
Testimonials:
What
our clients are saying about the Los Altos feeding Clinic.
Amanda and Matt, parents of Mya (2-years-old), Indiana

Our daughter Mya was born at 37 weeks by c-section since she was breech. There were no complications with her delivery to speak of. At only a few days old we noticed that Mya did not show a lot of interest in breastfeeding or taking a bottle. Her weight was increasing and her pediatrician did not seem to be worried.
As time went on the resistance to the bottle grew. She would start to cry at the sight of a bottle and even cry when we tried to feed her. We saw a GI doctor and he said she was having silent reflux. Mya was placed on a variety of medication but nothing seemed to help for more than a few days at a time.
We finally were able to be seen at a local Children’s Hospital and found out that Mya was aspirating milk into her lungs. She had a NG tube placed at 4 ½ months of age and got a g-tube at 8 months old. Mya never had vomiting problems prior to her experience with a feeding tube. After she got a tube she would vomit up to 4-5 times a day. We tried everything to help her including medication, using a feeding pump, doing a night drip, spreading out boluses over an hour, etc.
My daughter saw 3 different feeding therapist prior to coming to Los Altos Feeding Clinic. She had numerous tests done and everything came back normal. Mya had even passed her swallow study! So basically we had a 19 month old child who had no medical reason why she could not eat or drink but basically just refused to do it. After trying local feeding therapy for over a year I knew that we had to do something. Mya’s weight gain was almost non-existent and she had fallen off the growth chart completely.
Thankfully we found the Los Altos Feeding Clinic and now after 8 weeks of therapy Mya is eating over 1000 calories of pureed foods and drinking 24 ounces of milk a day!!! She has been off her tube 100% for over 6 weeks now!!! She is back on the growth chart and has gained almost 2 pounds! It has been amazing watching her grow and not be hooked up to a tube for several hours a day!
Ben Zimmerman was there for us every step of the way and always available to answer any questions we may have. We never felt rushed through appointments and we even did therapy 7 days a week to keep Mya off her feeding tube! Although at times we have felt that this journey has been a roller coaster ride we know that one day we are going to get off this roller coaster for good!
Ben has been able to get Mya’s extreme vomiting and gagging problem under control and at times I truly wondered if it were ever going to be possible! Now we realize with the right help anything is possible! Ben Zimmerman has such a passion for his career and it shows!! We couldn’t have made a better decision for our daughter!
Shwetha, mother of a 5-month-old
Our younger son was born full term and was healthy the first couple of months. Starting at 2 months, he slowly developed a refusal to feed, and was diagnosed as having acid reflux. Our pediatrician sent us to a GI, and the GI tried a bunch of medication - zantac, prevacid, erythromycin et al and a slew of tests.
After over 2 months of trying various options, we found that he had started to lose significant weight, and had fallen off the chart. The GI was concened that he was "wasting away", and was at risk of being declared Failure to Thrive. She wanted to intervene right away by geting a tube in him - and I was in tears right there. What had happened to my healthy little baby? Being very concerned about this approach I begged for time. The GI gave us all of 3 weeks and suggested that I reach out to Ben for feeding therapy. Those 3 weeks turned out to be life saving for our then 5 month old.
Ben started feeding him a bit of solids (the baby had never had solids before) and some milk at every feed. And feed over feed, we started to see a gradual reduction in his refusal and his vomitting, and a slow and steady increase in his appetite and eating. We were very encouraged and hope was renewed all over, but were still under pressure from our doctors, who wanted to see rapid weight gain happen. I was skeptical if that was even practically possible, it seemed to me the doctors wanted magic.
We expressed our concern to Ben, who without hesitation decided to provide round the clock feeding support to our baby to get us over the hump. For the next couple of weeks, Ben would feed our baby every 4 hours from 6 in the morning, until 7:30 at night, weekdays and weekends alike. There were days when I was tired and exhausted, but every single morning Ben would be there before I was, bright,and positive and encouraging, ready to feed my little one. And soon enough, within days the baby started to show dramatic improvement in appetite and eating and weight gain. The refusal and vomitting were starting to disappear too.
Over a period of 3 weeks, he gained over 3 pounds, and his feeds were going from long, difficult, crying sessions to quick, efficient, happy meals. The baby too, was having a lot of fun - laughing and playing and squealing at mealtime. His biggest smiles of the day were now for Ben. The magic the doctors had wanted, had indeed happened - thanks entirely to Ben.
Ben then worked with me to teach me to do the feeding myself. He was wonderful as a teacher too - patient and encouraging, and still methodical and persistent, fully understanding and supportive of a parent's needs. We now leave Ben's clinic as immensely relieved, happy parents of a healthy baby. My baby who had been born textbook-healthy and perfectly normal, and had this difficult, but common problem has now gone back to his happy, bubbly, cheerful self. I don't even remember how things got so bad so quickly, all I remember now is Ben's support helping us get back to the wonderful place of happy parenthood.
Craig, father of James (8-years-old)
Dear Ben:
I want to thank you for the incredible results you were able to achieve with James and finally solving his eating problem that no one else could.
As we told you, prior to learning about your clinic we had taken James to three other places to try and solve James’ extremely selective eating habits. We first saw a physician in Palo Alto who believed that James was sensitive to foods based on sight, smell, and texture and that this could be related to the very far end of the autism spectrum called Asbergers. This physician stated that since James was performing above grade level at school, was good at athletics, way far above grade level in math, etc. that this further confirmed his finding because medical studies showed that such children with similar eating problems have these same characteristics. This physician referred us to a specialist in San Francisco who confirmed this finding. After many discussions and treatment plans with the San Francisco specialist James did not improve.
Following this we went to an occupational therapist located in Arizona. She was so well known that people from all over the world came to see her. Her finding was the same and we then implemented her approach to no avail, and, of course, at a continuing considerable expense.
We then went to Stanford University and enrolled in their plan. Stanford also confirmed that James was obviously very selective with food because of how he viewed the sight, smell, and texture of it and that he had to be desensitized to this. They also stated that James was not placing food in his mouth correctly where the proper taste buds could in turn produce a positive sensation for food. We went through their program with no change in James’ eating.
During this time James who was now age 8 was continuing to lack adequate nutrition needed for proper mental and physical development. Our family could not travel because the very few food items that James would eat would not necessarily be available. James’ problem affected the entire family in many different ways and even caused major arguments between me and my wife as to how to deal with this matter. Finally our new family pediatrician told us about you.
Before we saw you James would act like we were killing him if we asked him to try an unfamiliar piece of food that was no larger than a grain of salt. If we insisted that he eat it he would cry and beg us not to make him eat it. It was a horrible situation to witness. To see James sit at our at our kitchen table today and feed himself four different food items, some of which he had never seen before, was remarkable.
James is now willing to eat anything placed before him, even oysters. I do not think that I could even eat an oyster. James may not be completely happy with what he is eating but he will nevertheless eat it without a fuss. This is light years ahead of where he came from and you were able to accomplish this in all of 8 weeks. James has gained weight during the last 8 weeks and is now at his proper weight. It is nice to no longer see his ribs show.
Our household in no longer in a bunch of stress over this, my wife and I are no longer arguing about the problem, and we can finally travel and enjoy a summer away from home. We are now taking our first vacation in years and are going to Hawaii this July with other trips planned thereafter.
I wish I could say more than just thank you. I truly hope you will remain in this profession because you are a rare find and many children will need you. Again, thank you so very much.
Very truly yours,
Craig
Michael and Belinda, parents of Ivy (2-years-old), Australia
“No Gastrostomy needed”

.....are the words Belinda and I have longed to hear for the past 18 months.
One of our twin daughters, Ivy, has had a rather challenging start. Our girls were born at 24 weeks in Westmead Hospital, Sydney and required a huge amount of care for the 1st 3 months of their lives.
Molly left hospital first escaping any complications that often arise in babies the premature. She is two and half and doing very well.
Ivy however, has had to deal with hydrocephalus, meningitis and an ensuing 8 neuro operations plus laser eye surgery.
Ivy pretty much had an NG tube from 2 months old and this coupled with a severe gag reflex and gastro intestinal reflux has made feeding her a big, big issue.
We were fortunate enough to have a paediatric gastroenterologist who was all for minimal surgical intervention and kept on delaying Ivy’s inevitable gastrostomy. My wife and I were very reluctant to have Ivy put through the operation for three reasons:
- The increased risk of infection to Ivy’s brain via the two v.p. shunts she has
- The burden of yet another operation
- My wife’s gut feeling that we should avoid this operation entirely. (I have a healthy respect for my Wife’s gut feeling).
The Gastrostomy loomed and at our last visit (Sept ’08) to the Gastro-enterologist it was arranged that I meet the surgeon and be taken through the procedure.
We also went to a 2nd Hospital for more information and hopefully a second opinion.
Both hospitals ended up giving us a date for Ivy’s gastrostomy, one for the 15th December 2008 and the other midway through 2009.
It was at this time that my own investigation for an alternative had led me to contact Ben Zimmerman at the Los Altos Feeding Clinic in California and after talking extensively with Ben and his previous clients we decided (against the advice of all our doctors, speech therapists etc. )to leave for California in early November to attend the Los Altos Feeding Clinic for 6 weeks.
I am so glad we made that decision and am very grateful Ivy had this opportunity .
Needless to say we were anxious about travelling half way around the world with Ivy to undergo treatment that we or anyone we know had no experience or prior knowledge of. Anyway the results speak for themselves. On the 3rd day, Ivy’s NG tube was discarded. At 21 days she had gained 2kg. At 4 weeks I took over the feeding and on the 23rd December after 6 weeks we landed back in Sydney with no tube.
I found the next weeks tough getting Ivy used to another feeding environment, recovering from a 13 hour flight and having to be solely responsible for her feeding but Ben is only a phone call away and we have regular calls about Ivy’s progress.
At home I alone feed Ivy in a closed bedroom away from distractions. She has bad days but overall progress is phenomenal. The food is a smooth puree still and probably will be for another 6 months. As yet her hunger cycle hasn’t kicked in but it won’t be long till she’s dragging the food off the spoon.
Ivy still gags and coughs throughout her meal but to a much lesser degree than when we first returned and it’s a rare thing now to see her vomit during and /or between meals, unless she’s constipated.
Personally, I envisage Ivy will be sitting and eating with us at mealtimes in 2 months time but I will be guided by Ben on this.
All in all, our experience at the feeding clinic was very, very positive and to have Ivy off the ng tube and off the feeding pump, her face free of tape, her lovely sound sleep, and huge reduction in reflux is a wonderful dream come true......we are incredibly thankful to everyone involved.
Michael Trehy

Amy mother of Julia (5 months)
My second daughter Julia was born full term. Healthy and happy things started off pretty normal for her until we noticed some excessive spitting up. Little did we know what was lying ahead for us. Julia ended up having a very severe case of Reflux which made her very uncomfortable.
At only 5 weeks she began refusing to nurse and refusing to eat completely. We thought she was going through a rough patch and that it would pass soon. After weeks with no change we got worried. At Julia's 2 month check up she had barely gained any weight and was diagnosed as Failure to Thrive.
We immediately took action to try to get her weight up. We began trying to force feed her. I literally would sit there for hours and hours each day trying to get her to eat just 2 oz. Every single feeding was an absolute nightmare. Julia would just cry, scream, kick and do what ever she could do to not eat. It was heartbreaking to see my baby go through this several times a day. Eventually, from exhaustion she would fall asleep and only then when she was passed out would she begin to eat tiny bits. The worst part was after all that she would then vomit all the food we had just worked so hard for.
After many doctors appointments her pediatrician prescribed her Zantac. That ended up being no help. Julia was then referred to a GI specialist. Her GI doctor changed her medication to Prilosec and said that would do the trick. Hoping the medication would help we waited for any sign of improvement.
After weeks, then months of no change we were frustrated. No doctors could offer her any help so, desperately my husband and I turned to the Internet. We found a few options but the one that stuck out to us was Feeding Therapy. Until then we never knew such a thing even existed. We then asked our Pediatrician to refer us to a feeding therapist. They sent us to one at our hospital but after our first visit we knew she was not qualified enough to handle Julia's problem. It was very disappointing.
From there we turned back to the Internet and found Ben Zimmerman at the Los Altos Feeding Clinic. After reading so many great reviews it felt like the clouds had parted and there was finally help out there for Julia. We quickly made an appointment to get Julia evaluated and after just seeing her once Ben said that she was going to be an easy case and he knew exactly how to handle her. I left the appointment completely hopeful. Finally there was someone out there to help my Julia! After months of agony there was finally hope. Today Julia completed her 5 weeks of Therapy. Ben's technique was absolutely what Julia needed. Never once was he too forceful and after each session Julia would come out happy, smiling and laughing.
After only two sessions her feedings went from one hour plus to just 20 minutes. Incredible! She started her therapy as a baby that would not eat and today she is a baby that is opening her mouth to eat solids and drinking out of a cup. I know we still have fine tuning on some things but we're definitely on the right path and Julia is climbing up that growth chart. To say thank you to Ben would not be enough. He has made Julia a happier baby and that to me is a special gift. Thank you so much Ben! Amy Goldammer
Manilla mother of Nida (3-years-old)
My daughter was a premie (27 weeks) and weighed 2 lbs. 4 oz. She had a hemorrage in her brain on both sides that caused hydrocephalus. She required a vp shunt when she was 3 months old and had 5 surgeries due to shunt malfunction and one time it got infected.
They started her on my breastmilk through an NG-tube when she was one month old. She could suck for 2 months. Half of the feeding was through a bottle and when she would get tired the rest would be fed to her through the NG tube. After the surgery for vp shunt, she lost her sucking reflex.
When she was discharged from the hospital at 7 months old, she came home with the NG-tube. I hated to put the G-tube. When she was one year old, she started vomiting and had diarrhea. We were changing the formula, but her condition was still the same. Finally the GI MD said that the NG-tube might be the cause because it is not supposed to be for long-term use. So we had to put the G-tube.
I have tried going to so many OTs, but nobody could help her with eating by mouth. One day I was in the waiting room of one of the OTs and I saw a 3-year-old with an NG-tube. I started talking to the mom. She told me about an OT whom her GI doctor from Lucile Packard Children's hospital had just referred her to. I got really interested because that OT was referred to her from the GI MD. She was also planning to see Ben Zimmerman.
We exchanged phone numbers and that is how I got Ben's phone number. I always thank God for the day that I met that woman who gave me Ben's number. He was the answer to all of my questions. Listening to other people's success stories in Ben's waiting room was giving me more hope that my daughter would eat by mouth one day. And yes she is now. She is 3-year-old now and it is almost one year that she can eat.
Benjamin there are no words that I can find to thank you enough. Each time when I feed her I pray for you. My prayers will always be with you.
Thanks a lot
B., mother of S. (1-year-old)
S. is a premature baby, born at 8 months. He was taking bottle for the first four months of his life and then started refuse the bottle. It progressively got worse over a two week period and then he stopped taking the bottle completely.

We live in UK and at that point he was admitted to a hospital for an assessment. The doctors in NHS had been proposing gastro oesophageal reflux could be the main contributor for this condition. However, he was not vomiting much beforehand. Investigations point of view he only had blood and urine test to rule out any infections which came back negative.
In the mean time he was started on NG top up feeds. After NG tube was inserted, his oral intake became much worse. Also, he started gagging and vomiting multiple times in a day. It was very difficult and painful for us to watch him gagging and vomiting where he throws up the tube and it took about 10 minutes for the gag to settle down.
After the NG tube was inserted we could only give him 2 oz. feed at a time to prevent him vomiting and we were almost feeding him 24 hours a day. However, even with that it was difficult to establish a reasonable feed. He dropped off from his growth chart and development got delayed.
We were looking for some place in the NHS which specialises in taking children out from the tube feeding. We could not find any hospital in NHS provide such a care even the Great Ormond Street Hospital, one of the biggest children hospital NHS does not have a specialist with successful cases of kids coming out from the tube feeding. Also, we could not find places in the Private health care, UK providing such service. We felt that our Speech and Language therapist in UK and her action plan would not help him to come out from his tube feeding at all.
Our Speech and Language therapist in UK asked us to start him on solids and said he would get better afterwards. It was very difficult to make him take solids as well. We were very disappointed and started to look else where in the Europe and the rest of the world.
Only in US we found this specialist treatment programmes after months of research in the internet. When we found Los Altos Clinic and reading their successful stories of children coming out from the tube feeding we felt our prayers are answered and the divine showed us some help. We contacted the clinic which is very helpful and a gave a lot of parents contacts whose children were treated here and came out from tube feeding. We decided to take the big step as last resort to prevent him going to have G tube eventually.

His therapist Ben was very helpful and according to his treatment protocol he has been eating and drinking by mouth and gaining weight. He also restarted to take the bottle. We would like to thank Ben for the wonderful service he provides to these type of children.

Mary
–--Mother of Zach with multiple food allergies
and reflux
My
son Zach is 22 months old. At two months of age
he began arching his back and refusing to nurse awake.
Blood appeared in his stool and spit up, and he developed
eczema. He was diagnosed with a dairy allergy
and gastroesophageal reflux disease, but despite trying
an elimination diet and Zantac he continued to refuse
food when awake (both liquids and solids). His
weight gain stalled, dropping from the 50th percentile
to below the 5th percentile over the next 6 months,
and he was diagnosed with a feeding aversion and failure
to thrive.
Subsequent
RAST allergy testing revealed that Zach had multiple
food allergies, and at one year of age he was put on
100% Neocate hypoallergenic formula. His reflux
medication was also changed to Prevacid, and then to
Prilosec to see if that would help. By the time Zach
was 18 months old we felt that his allergies and reflux
were finally under control, but he still continued to
refuse food. His eating was 99.5% from a bottle
and mostly while asleep, and his weight remained around
the 5th percentile.
We
consulted speech/feeding therapists, several GI doctors
and a nutritionist, and had numerous tests done (upper
GIs, endoscopies, colonoscopy, etc.) to see if we had
missed something. Meanwhile, every day we counted
each ounce of food he consumed and struggled desperately
to give him the minimum amount of calories he needed
in order to keep him from dropping off the growth curve
completely and needing a tube.
All
of that changed when we brought Zach to the Los
Altos Feeding Clinic. On the very first day,
Ben was able to get Zach to eat pureed foods from a
spoon, and in quantities we couldn’t believe.
Before coming to the clinic, the most pureed food Zach
had ever eaten at one sitting was 2 oz, and that was
rare. But Ben fed him 7 –8 ounces at each meal
that first day, and in only a few minutes! By
the end of his therapy I was feeding Zach up to 11 oz.
of food per meal (purees from a spoon and formula from
an open cup) and he had gained 1 pound.
It
has been almost three weeks now since we returned home
from the clinic, and we have been able to continue feeding
Zach very successfully using the protocol Ben taught
us. Although he has a ways to go before he is eating
age-appropriate foods, we are amazed at the progress
he has made, and thrilled to see that his weight has
already climbed back up to the 25th percentile! He also
has so much energy I can barely keep up with him.
Prior
to coming to the clinic, we had Zach evaluated at the Kennedy Krieger Institute (KKI) in Baltimore. They
told us we would have to wait 6 months to enter their
intensive Day Treatment Program, we would need to be
there for 8 weeks, and in the meantime they would recommend
that we get Zach a G-tube! When I heard that,
I knew we had made the right choice in coming to see
Ben first – even if it meant we had to travel
from the East Coast to California.
Unlike KKI, Ben was able to see us within a few weeks,
he completed our therapy in less than 5 weeks, and he
is committed to keeping kids OFF the tube, which was
exactly what we wanted for Zach. He also provided
just the sort of supportive environment and tailored
flexible program we were looking for.
We
are SO grateful that we found Ben and the Los
Altos Feeding Clinic!!! If your child has feeding
issues, we cannot recommend Ben’s program highly
enough.
Sara---
mother of 11 year old
My daughter Ria has cerebral palsy from birth.
I am her mom Sara, and a scientist by profession.
As a little baby Ria had a lot of oral sensory issues
and through the first few years of her life she had
a lot of feeding issues, particularly fussy about what
and how much she wanted to eat. This gradually went
away and she turned out to be someone who enjoys eating
her meals. However drinking continued to be a big issue.
Ria
almost always refuses to drink and the only thing I
can get her to even consider drinking is water. Her
teachers at school are always complaining about how
little she drinks and how she refuses a drink any time
she is asked or offered. Additionally she always showed
extreme aversion to cold drinks.
We
approached Ben Zimmerman with this dilemma a few months
back this year to see if behavioral therapy may be a
way to help Ria with this challenge. Ben was recommended
to us by some of my friends who had success with feeding
challenges in working with him.
Additionally
many of these kids were from the autistic spectrum so
I wasn’t sure if Ben would work with a child with
CP. I was pleasantly surprised that Ben did not
approach the child from their diagnosis and actually
felt that behavioral therapy can be applied to any child.
Additionally his work was not restricted to feeding
alone but drinking could also be tackled in the same
manner. With this information we started our sessions.
Ben
was able to within a few sessions get Ria to drink a
significant volume of drinks and also increased the
variety of drinks she would take. He was able to get
her to drink water, milk and juices at cold and warm
temperatures.
We
found Ben to be fantastic in his style of interaction
with Ria being steady and compassionate. He also
was able to explain what he was doing and why he was
doing it, very clearly to us, which allowed us to understand
the process better and helped in our follow-through
at home. I was also impressed by how systematic Ben
was in his approach.
We
have now been working with Ben’s protocol at home
and Ria continues to drink more than she every did before.
It is exciting to see this progress and we look forward
to continuing the work so that she begins to really
ask for the drinks one day. The great thing is that
Ben is also a great resource and is always available
to answer questions.
I
highly recommend this method and Ben to anyone who has
a child with any diagnosis or no diagnosis but who simply
has challenges in feeding and drinking.
Amanda mom of Caitlin (6-months-old)
As a member of Kaiser Permanente since 1999, I would like to provide feedback regarding the feeding therapy services referred by Kaiser Santa Clara.
In March of this year, our first chilid, Caitlin, was born with multiple birth defects. She had two heart defects (ventricular septal defect and coarctation of the aorta) and tracheoesophageal fistula. By three months old, all of her defects has been surgically repaired but we were left with the chronic challenge of feeding her. Caitlin had required an NG feeding tube since birth and at the time when her surgeries were completed, she still only took half of her required calories orally.
In June, Caitlin was referred to the one feeding therapist Kaiser contracted with at that time. We worked with this therapist from June until August with very little progress. Each week we would drive a half hour each way (from Santa Clara) to simply sit and discuss what I had tried at home the previous week. The last twenty minutes I would attempt to feed my daughter while the therapist observed and gave feedback. She mentioned that she prefers to have the parents feed during the session instead of herself. As soon as my daughter fussed, we would stop and try a new method. This went on week after week until I realized it was a complete waste of time.
During the time we were at UCSF for Caitlin’s heart surgeries, one of the occupational therapists had told me about Ben Zimmerman at the Los Altos Feeding Clinic. I gave him a call after three months of using the Kaiser referred feeding therapist and he agreed to work with my six month old daughter. At that time, I also contacted Caitlin’s pediatrician with the intent to work with Mr. Zimmerman. She made the referral and happily, it was approved.
Caitlin started seeing Mr. Zimmerman twice a week at the beginning of September and the immediate difference I noticed from the other therapist is that he did the work of feeding my daughter and assessing her troubles. We slowly increased our frequency of visits as he familiarized himself with her challenges and finally diagnosed and proposed treatment as an “intensive case”. He suggested we work with him daily for a minimum of two weeks in order to break her dependency on the feeding tube.
We agreed to this and spent twenty-six straight days at the Los Altos Feeding Clinic, including weekends, in order to teach Caitlin how to eat normally after being tube fed for the first six months of her life. We had made this committment knowing that the only other option was a G-tube placement. Another surgery would have been a tremendous strain physically, emotionally, and financially.
After the first five days of intensive therapy, Mr. Zimmerman was able to remove the NG tube with the confidence that he would be able to keep it out. He did the feedings for the next two weeks until it was time to train us, Caitlin’s parents, on her specific feeding protocol. We were able to learn quickly at which time we all agreed she was able to be discharged from the intensive program.
Throughout all of Caitlin’s medical experiences this past year, Mr. Zimmerman has made one of the biggest impacts on our family. I have never encountered a more dedicated, hard-working, medical professional who would do whatever it takes (with the parents consent) to get his job done. Caitlin has been steadily gaining weight and developing normally for the last three months since we removed the feeding tube. We will forever be indebted to Mr. Zimmerman for what he has done for our family and Caitlin’s quality of life. I would highly recommend Mr. Zimmerman and the Los Altos Feeding Clinic to any family with a child six months or older who has a feeding problem. If the parents stay the course, he will likely get the job done of breaking a child’s feeding tube dependency.
Ted and Judy Wise, parents of Alex (4-year-old)
We never imagined we would be writing a testimonial about a feeding clinic. But Ben Zimmerman at the Los Altos Feeding Clinic has made such a profound difference in the life of our son, Alex, that we felt other parents who are experiencing the eating challenges we have faced needed to know there is a place where they can find a solution.
Our son, Alex, is a healthy 4 ½ year old with no medical problems but had a very limited diet of cheerios, yogurt, goldfish and occasionally french fries and bacon. We had tried everything to get him to change his diet -- lots of praise, bribery with toys, begging, offering him only new food as advised by our pediatrician (we caved after our son refused to eat for more than 36 hours), not making issues with food but none of these strategies worked. He would refuse, adamantly, saying he was “scared” and in a rare moment when he would take a bite of something new, he would gag and cry. We tried to get help – we read more than half a dozen books on pediatric feeding difficulties, we consulted several pediatricians, we had Alex checked by pediatric GI to make sure there weren't any stomach/digestion issues and even took him to a child psychologist. None of the strategies worked and none of the specialists could offer a strategy that would address our son’s eating issues.
Frustrated, we searched further and found the Los Altos Feeding Clinic. In the first weeks Ben focused on broadening the range of tastes Alex would eat by using pureed foods. These were the weeks when Ben showed Alex how past behavioral tactics that he had used with us would no longer work. At moments it was challenging but we were impressed at how well our son responded to Ben. Then there was the first session where Ben introduced solid food (hot dog and an apple) and we just about fell off our chairs as we watched Alex eat with a smile on his face. It was remarkable—and it just got better from then on. After a 5 week program of 3 sessions per week, Alex now eats EVERYTHING!! You name it, Italian, Mexican, Asian, any vegetable, fruit, salads and even sushi!
Today, we are just floored by the outcome and truly grateful to Ben Zimmerman for his “magic”. We are extremely proud of our son and very relieved to have his eating issues resolved. It wasn’t until we went through the program at the Los Altos Feeding Clinic that we realized what a toll the eating issue had taken on our son. Today, Alex is very proud of his eating accomplishments, confident, happy and eager to try new food. Amazing!!!
Amutha, mother of Shiva (3-years-old)
My name is Amutha. My son Shiva was born premature at 24 weeks. Four months after coming home from NICU he developed severe oral
aversion due to infant GERD. We had to put in a g-tube since he had not
gained eight in four months. Over the course of two years we worked
with at least 5 different Speech Therapist , an OT , nutritionist and
psychologist for his feeding. He did take 4 oz of yogurt with lots of
distractions. Whichever way I tried the maximum I could get him eat was
400 cal orally. The aximum he would take both oral and tube feeding combined was 960 cals. He had a super sensitive gag reflux. He gagged
and vomited with almost all the meals. He used to vomit at least once a
day even when I was not feeding him orally. We did the overnight
feeding. Me and my husband used to co sleep with him everyday in fear
of running to ER in the middle of night with his detached g-tube in
our hands. That has happened only 4 times in two years and he almost
strangled himself once in a while when he was asleep. Why would we not
sleep peacefully :). The days went by me feeding him over half an hour, spending another hour with him to making sure he would not laugh or
cry. If not he threw up and the entire process started again. This
happened four times a day for his breakfast, lunch, snack and
dinner.
When he was 28 months old the developmental pediatrician said he was it
risk for becoming mentally retarded. We needed to eliminate his tube
feeding and get some time, energy and good sleep so we can concentrate
and look at his deficits and work on his overall developments. I knew
in my heart my son is not mentally retarded. I knew if he started eating by
mouth there is this whole other world waiting for him to explore. We
decided to come to Los Altos Feeding Clinic. After working with Ben
Zimmerman for a total of 29 days we are going home with my son being
completely tube free. He has been tube free from the end of second
week into the program. He is now feeding 6 oz of purees and 6 ounces of
liquids for each meal three times a day. His total calorie intake is
now 1500 calories and he is thriving. I forgot to mention he takes his
meals in less than 8 minutes. I am saving so much time I can actually
start to work on his other developments. I have already started to see
lots of developments in all areas. I heard about Los Altos Feeding
Clinic some time in mid of 2007. I regret that I didn't come here at
that time. He would have caught up in his developments by this time.
Maria, mother of Jack (age 7)
We have recently returned to New York from a 3 1/2 week intensive program at Ben Zimmerman's feeding clinic. My son is seven years old and suffered from extreme food selectivity. At age 2, he started gagging and throwing up on food and started severely limiting his food intake and variety.
My life for the last five years has revolved around trying to get him to eat and spending sleepless nights worrying because he did not. His diet consisted of white bread(no crusts), white bagels, pancakes, waffles, french fries, yogurt (smooth texture) and pretzels (he had no problem with junk-cakes, cookies, candy, chips, etc). He refused all fruits, vegetables, meat, eggs except for the occasional chicken mcnugget. He also had alot of weird rituals with food-ie. had to be the correct temperature, pancakes only for dinner, only eating half of each cracker, etc, etc, etc., etc!!
Also of note is that at age 2 Jack decided he did not like being barefoot. He has worn socks 24 hours/day ever since--in the pool, on the beach!!! He would FREAK out if anyone tried to remove them. I gave up and got him speedo "swim socks"! Jack has undergone 3 years of occupational therapy for his eating issues and for sensory integration disorder, at one point going 3 times a week for the eating specifically. We have taken him to at least 3 different psychologists, a speech pathologist specializing in feeding issues and have spent probably thousands of dollars.
After extensive research online I found Ben Zimmerman. After 3 1/2 weeks of 3 meals/day/ 5 days/week, Jack was eating everything from sushi to spinach. It also took Ben about 2 seconds to get Jack to take his socks off! He has been barefoot-in the pool, in the sand- ever since! Jack came out of each session happy and proud of himself. I was shocked to see how he went back to the clinic so willingly everyday.
We have been home for 2 weeks now. The first few days were very hard. We have stayed consistent and each day is getting better and better. Ben is always there for phone consultation when you need him. The other night we went to a friends house and Jack had pizza and raw veggies with dip like all the rest of the kids. He went in the pool barefoot and without a shirt(another little quirk that Ben fixed!) All present at the party could not get over the change in Jack. Needless to say, we are thrilled. We can't say enough about Ben Zimmerman and would recommend him for anyone in the same situation. My only regret is that I did not get Jack out there sooner!
Michelle, mother of James (21 months)
James was a 25 week preemie twin who spent the first nine months of his life in the NICU. With underdeveloped lungs, James struggled to live and his ventilator dependency was the beginning of cause and effect situations. At two months old James underwent a tracheotomy due to subglottic stenosis, or scarring caused by being intubated for so long. It wasn’t until James was six months old that a bottle was introduced using a Haberman nipple and eight months old before he was able to consume enough volume to stop the supplemental NG feedings.
Because the plan was to reconstruct James’ trachea around his first birthday, it was the opinion of all (Drs., OT’s, PT’s, SLT’s) to not push him to eat solids until then; if he refused we would stop. At sixteen months, the doctors successfully reconstructed his trachea, the stint (inserted during surgery) was removed four weeks later, and after four consecutive weekly visits back to the operating room for subsequent scar revisions (removal), James was decannulated on December 11, 2007. What was a momentous occasion was overshadowed by the fact that James left the hospital after the initial reconstruction refusing to eat anything and sporting an NG tube. No one anticipated his initial refusal to eat, not even a bottle, would develop into classic feeding aversion and NG tube dependency. Then the NG tube complications started. We were told he must have a sensitive stomach, as we had to watch the life drain out of him with each feeding as he violently gagged, turned colors and eventually vomited during his bolus feeds.
It was becoming apparent that James had forgotten the behavior of eating by mouth. We would be “starting from scratch” and even with weekly OT and SLT visits it was going to take a long time. The NG tube had been in for three months already and we found ourselves being referred to the GI specialist for discussion of G-tube placement. The date had been set, and the clock was running. By chance we discovered that there were intensive feeding programs, however the specialist informed us that most programs would probably not accept James until after the NG tube was removed. Fortunately my husband took it upon himself to not be discouraged. He found Ben Zimmerman and the Los Altos Feeding Clinic website on a Monday, met with Ben on Wednesday and relocated our family to a hotel two hundred miles from home to start the program the following Tuesday. Ben passionately agreed that we needed to atleast try intensive feeding therapy BEFORE we allowed James to go through yet another surgery, and while I thought Ben was maybe too confident, my hesitation was replaced by hope.
I am thrilled to report that today was our seventeenth day in the program and we will be going home tomorrow. Ben removed James’ NG tube on the second day and assured us it would not need to be replaced. James is eating three meals a day each consisting of 5 ounces of pureed food and six ounces of milk. We are amazed with the changes we are already seeing in him; he is stronger, more active and even his hair has filled in.
We have tired of speculating in all of James’ miracles what was the “thing” that did it…What allowed him to get over pneumonia for the last time? What was it that Ben did that succeeded where all others had failed, or rather not dared to venture? All we know is that we have a fighter who had never been comforted by eating, whose entire lifetime of experiences having to do with his face involved invasive tubes, tape and gloves. We did not anticipate that the intensive feeding program would be easy, nor do we think that the upcoming weeks and months will go without a hitch. We do know that our sacrifices will be worth it and that with each day we should see improvement. Finally, we are going home without a “tube.”
Kirstin Dahm, mother of Haley (10 months)
My daughter Haley was born with Pierre Robin Sequence at 32 weeks and severe acid reflux. She had a jaw distraction at Stanford Children's Hospital at 6 months of age to make her jaw bigger. It was a very successful surgery and the Plastics team did an amazing job.
After her surgery the plastics team kept asking me at each appointment "Is she eating?" The answer was always the same "No." The team could not understand why she was not eating. Haley still had a cleft pallet but it should not have prevented her from eating. We had an upper GI scan and all was normal. She had excessive vomiting, and an extremely sensitive gag reflex.
When Haley was 4 months old I started seeing an occupational therapist at Lucile Packard Children's Hospital. Each meal I would spend playing with Haley's food, getting her familiar with the small, taste, and touch. I even taught her to play the drums with the spoon, but she wouldn't eat.
At ten and a half months, she had never eaten food by mouth when we came to Los Altos Feeding Clinic. The occupational therapist had discouraged me from coming and said to me "It’s all about volume there." I thought to myself "Well, it’s all about volume for me too. I need her to have enough food to grow and gain weight." So then I had to read the website. I was even more convinced. No one else I had talked to or met with had a plan to get Haley off the NG tube. When I read what other people had written I thought, these other children have much bigger problems than Haley and if he can get them off the NG tube, maybe they can get her off the tube too.
So we came to Los Altos Feeding Clinic and Ben Zimmerman got Haley off the NG tube. This has meant so much to me because she was scheduled to have surgery for a Nissan and for a G tube, and now she needs neither. He prevented her from having unnecessary surgery. I am so grateful. I just wish I had known about Los Altos Feeding Clinic sooner. I am more than happy to talk to anyone who has feeding problems with their child and they want to know more about our experience.
Watch video: See Haley Eat
Uma
- mother of 5 year old twins
My daughter Nitya went from eating nothing by mouth
to completely getting all her nutritional needs met
by oral feeding in just 10 weeks. My name is Uma and
I am mother of 5 year old twins (two of surviving 25
week preemie triplets). My daughter Nitya came home
from the NICU at 5 months with a G-tube. Following that,
at 8 months she was on tracheotomy for the next 3 years.
During this time she was not eating by mouth at all
and was followed by OTs for oral-motor sensory issues.
Since her decannulation in Dec 2004, we tried several
approaches: home cooked blenderized food through G-tube,
getting her to be hungry, sensory approaches, etc. all
supervised under an OT - but these did not get her to
eat by mouth. In March 2006, my occupational therapist
suggested that I contact Benjamin Zimmerman at Los Altos
Feeding clinic… Now I am feeding her at home and
this has been such an amazing experience for us to see
her accept food by mouth.
Also in the last 5 years we could not get Nitya's teeth
cleaned. Her dentist suggested that she may need general
anesthesia for a complete cleaning. Well, now since
we started the behavioral therapy she is allowing me
to brush her teeth. She has also randomly spoken 20
words and is imitating babbling now. Nitya has made
tremendous progress in the last few months.
Watch
video: Nitya
now self-feeds
Audrey
– mother of Vivian (18 months old)
Vivian was a 35 week preemie born at 4 pounds
5 ounces and 15 1/2 inches long. At birth her right
lung collapsed. She remained in the NICU for over a
month. During her stay she had her first genetic test
which came back negative for major syndromes, such as
Down Syndrome. Vivian has been tested for over 100 genetic
syndromes, all negative. She was unable to eat much
due to her vaulted palate, bifid uvula, and a submucous
cleft. Vivian had every test (swallow study, upper GI,
etc.), every evaluation (speech, ENT, GI, etc.), and
also seen a ton of specialists all over the country.
No one was able to do much about her eating. She had
been able to suck from a bottle for a few months and
eat about 1/8 a jar of baby food.
When Vivian started eating less and less, we turned
to the Los Altos Feeding Clinic in July of 2006 after
finding them on the internet. Vivian was at the Los
Altos Feeding Clinic for a total of 5 weeks. During
that time various techniques were customized by Ben
Zimmerman to help Vivian to eat. By the end of the 5
weeks I was doing all food preparation, calculations,
and feeding. Vivian went from taking 690 ccs of Pediasure
to eating up to 1680 calories by mouth!
Linda
- mother of 26 week twin preemies with cystic fibrosis
My 6 year-old twins were born at 26 weeks
gestation and were on ventilators for the first 3 months
of their lives before they were finally diagnosed with
cystic fibrosis, a genetic illness which affects the
lungs, pancreas and other mucous producing organs.The
long intubation led to severe oral aversion, and the
increased acid production,common in children with cf,
led to reflux and emesis, contributing further to their
aversion.
After many years of feeding therapy that resulted in
little progress, we learned of Ben Zimmerman's clinic
through their Gastroenterologist's office and also through
a client whose older son attended the same kindergarten
as my son. I was excited by the progress of her toddler,
and called the Los Altos Feeding Clinic for an appointment
for my twins in May of 2006. 5 months later, they are
no longer tube dependant, they are drinking the special
high-calorie formula they have been getting through
the tube since birth, and they are eating calorie enriched
baby food for the first time in their lives. What is
especially remarkable is that all of this was done without
having to resort to the technique of introducing hunger
to them - which is something we couldn't do because
maintaining a high calorie diet is essential to the
health and well-being of children with cystic fibrosis.
For the first time, we are looking forward to a future
in which my children can enjoy food and all the social
milestones where food plays such an important role.
Thank
you Los Altos Feeding Clinic and Mr. Zimmerman!
Helen
--- Mother of Rebecca
Rebecca
is 2 years old, she has a rare metabolic disorder (UMPS),
which means that she can’t produce enough energy
to grow & develop. She has been diagnosed with failure
to thrive and developmental delay.
She was born at 2.5 kg (5.5 lbs) and from the start
had difficulty feeding, she had recurrent thrush in
her mouth and would not suck. She was weaned at 4 months
and seemed to enjoy solid foods more than milk but she
still did not gain sufficient weight. At 4 months we
were told there was something wrong and investigations
started. At 6 months Rebecca was placed on an NG tube
as her weight was so low. She remained on the NG tube
for 7 months, at this stage her doctors wanted to give
her a G-tube. Rather that let her go through this we
managed to wean her onto drinking from a cup and managed
to get her to drink sufficient high formula milk to
enable us to get rid of the tube altogether.
Rebecca was finally diagnosed when she was 16 months
old and was placed on medication. At this stage we felt
it was time to try and resolve her feeding difficulties
as she could now get the necessary calories and energy
from her food. All the interventions that had given
her nutrition had resulted in a complete phobia for
eating. She would not open her mouth for food, if we
managed to get any food in her mouth she gagged or vomited.
To get her to drink sufficient high calorie milk we
had to bribe her 8 –10 time a day with books and
music. Her weight gain was very poor and we were again
being threatened with the g-tube.
We are based in Ireland and had tried all the usual
food desensitisation programs. We searched the web but
could find nothing in Ireland or Europe, which would
actually make Rebecca eat without giving us advice or
starving her. Eventually we came across the Los Altos
Feeding Clinic web Site and it seemed to offer what
we were looking for. We spoke with Ben Zimmerman and
with other parents who had been through Ben’s
treatment and we were convinced. We took the 11hr flight
to San Francisco and did not look back.
Ben worked one-on-one with Rebecca and had her eating
solid foods within 2 days. He modified existing protocols
and developed new techniques to deal with Rebecca’s
food refusals. After a month Rebecca was taking 1200
–1500 calories orally she had gained 1lb and was
being fed 3 times daily. Each session taking just 30
minutes.
In the month since we came home Rebecca has gained 4lbs.
She has so much more energy and stamina – we never
expected that food would make as big a difference as
it has – but every week she seems to hit some
minor development milestone. We know that we would never
have got her to this level of eating without the Los
Altos Feeding Clinic and even better Ben continues to
stay in touch and help us fully refine her feeding process.
I have no hesitation in recommending Ben Zimmerman and
the Los Altos Feeding Clinic. It works. Thank You!
Jennifer
---- mother of Max who is 3 years old
Hi Moms,
I
recently began taking Maxwell, my 3 year old, to a feeding
clinic in Los Altos for severe food refusal. Those of
you who know me well, know that he has lived off of
milk, yogurt, cheese, and crackers for the past two
years (I am not exaggerating -- he has never eaten pizza,
fruit, macaroni, juice, etc).
I
have taken him to see several different pediatricians,
a nutritionist, an occupational therapist, and a child
psychiatrist, but until recently was unsuccessful in
finding someone who could help him. I had tried everything,
except putting him in an inpatient behavioral unit (i.e.
a hospital setting). I recently discovered the Los Altos
Feeding Clinic and started taking him there.
Before
going, he refused to try anything (he said he was scared
of the food and so on). He has some texture and sensory
issues, which is what initially started his food refusal.
Ben Zimmerman started working with him, and after only
a month, he is eating food at home (all pureed at this
point). We will be gradually increasing the texture,
until he is eating "real" food. My husband
and I are thrilled with the results so far and wanted
to share this information, in case you or someone you
know is in a similar situation.
Debbie ----Mother to Andrew (16 months old)
Hey there Moms!
My name is Debbie. My son Andrew is 16 months old. He
was born full term and weighed 8Lbs 12oz, however he
was born with congenital heart disease. At 2 days old
he had his first open heart surgery to repair his Aortic
valve.
At 7 weeks old he was still in the hospital and had
not gained any weight. He refused to drink by mouth.
Knowing he needed an other heart surgery, we knew he
needed to grow; therefore the next step was a G-Tube.
At 8 weeks old the g-tube was in place and Andy shut
down. He refused everything in his mouth; he would gag,
wretch, vomit and could only handle about 60 ccs/hour
on a continuous pump for 18 hours a day. Life was tough
for him and our family. We made it to 6 months for his
second heart surgery; a VSD repair and de-banding of
his PA valve. Andy came through the surgery ready for
life. He had much more energy.
We thought it was time to feed by mouth again. OT, GI's
and PT were absolutely no help what so ever. They'd
say stop feeding him by mouth the second he gags; I
would put a spoon to his mouth and he's gag so the feeding
would stop. Their theory didn't work.
After a 3 month wait we were accepted to St Joseph 's
in NJ for an intensive feeding program. The first day
there Andy ate 4 oz of peaches, so the doctors and behavioral
specialists told us to go home and we would have more
"FUN" feeding Andy at home. By this time Andy
was 1 year old. The next 3 months at home were no "FUN"
at all.
Andy shut down, it would take over and hour to feed
him 4oz of baby food and he wouldn't drink anything;
so back to using the g-tube forever at this point. Until
I found Ben Zimmerman at the Los Altos Feeding Clinic.
Thank God! Ben took Andy on within weeks of my first
phone call to him. Within the first week at the clinic
Andy was no longer using his g-tube for nutrients. After
2 weeks of Ben feeding Andy I got to try. Incredible!
Less than 30 minutes to feed Andy 8oz of food and 6oz
of milk. Real milk, no more formulas!!
We spent 4 full weeks at the clinic and then went home.
Everyday gets better, and faster to feed Andy. Ben Zimmerman
is a miracle worker; I had lost a hope of Andy ever
eating like a normal child, and Ben gave me back hope,
and a life. What he gave Andrew is much more. Andy is
talking, eating and walking. He is thriving in a matter
of a few short weeks. All I can say is trust Ben, he
knows!! And trust in yourself and your child that you
can get through the feeding by mouth; everyday is a
huge improvement. Andy has a chance now at a normal,
healthy life because he is eating by mouth. He is much
happier, he's personality has changed for the better,
even his color has changed from eating real food!!
Eileen--- Mother to Daniel (14 months)
We have used the Los Altos Feeding Clinic (LAFC) and
would love to share our experience with it. First a
lot of background on our situation. Our child, Daniel,
has oral aversion. In other words, he does not tolerate
things in his mouth, be it toys or food. This child
will literally starve himself to death given the chance.
At two months old, I found that he would react to nursing
as if he had reflux. Feed for a few sucks then yank
himself away, arching his whole body away from me, crying,
kicking and pushing. Nursing was brutal. We figured
out that he fed better when he was too sleepy to fight
us. So we would schedule his feedings with his nap time
– rock him asleep, and start nursing. At four
months old I was excited to start him on solids thinking
things would be different. We persevered with solid
foods for a good four months until he was 8 months old
with no progress at all. Then one morning he was intently
watching me eat a piece of toast, he seemed quite interested.
So I offered it to him. Daniel licked the toast and
a TINY speck (size of a pinhead) of a crumb was on his
tongue and he started retching. Immediately I swept
it out with my finger and called the pediatrician. He
said that that was definitely NOT normal and told me
to hold off giving him real solid food for now.
I continued trying the jars. If he was given the fruit
jars, he was retch the first few bites, and end us taking
most of the stage 2 jars vomiting approximately every
other day on them. If he was given a vegetable (peas,
carrots, sweet potatoes) or protein jar (beef and vegetable,
chicken noodle), he would retch, gag, and vomit at the
first bite and empty out the entire contents of his
stomach. Given how difficult it was to get the food
into him, we simply didn’t bother giving him vegetable
or protein jars anymore. He readily took the Yobaby
jars at first, then he started retching also, vomiting
approximately every other day on those too.
He required A LOT of toys and distractions, feeding
at the park, in front of the television, or in the bathtub
to take jars or yobaby. He required to be rocked asleep
for his milk feedings. Things were quite difficult with
a lot of cleaning up of his vomit.
The pediatrician referred us to O.T. specializing in
oral issues. We were then referred to GI after about
4-5 sessions with minimal progress. The GI said it was
classic oral aversion and there was nothing they would
do for us. Daniel even went in for an upper GI study
and swallow study. Results came back normal except for
the fact that he vomited during the study. She recommended
the Kennedy Kreiger Institute (KKI) (sp?) in Baltimore
Maryland where they have a behavioral feeding clinic.
She said that they have success with kids that they
can’t help. We were also seen by the Stanford
Infant Behavioral and Development Clinic across the
street from Lucille Packard Children’s hospital.
Everyone said that Daniel had severe oral/feeding aversion
but they all threw their hands up and said they couldn't’t
help and did’t know what to do. Then I read a
glowing review about the LAFC from a mom who had a picky
eater. If I recall correctly, this boy only ate dairy
items and breads. He had never eaten a sandwich or fries
or any “normal” food that a 3 year old eats.
We went in for an initial evaluation. Ben Zimmerman,
the guy who runs the place, observed me feeding Daniel
a jar. Then took over the feeding for the last a few
bites. When he was done, Ben said that Daniel was “a
simple case.” I was shocked because all the medical
establishment people had no idea what to do with Daniel.
Honestly I had my doubts. It seemed like too confident
a statement to make. We went in for another seven sessions
and Daniel came out like a different child in two and
half weeks. He now takes the protein and vegetable jars,
without vomiting. There usually is a retch for the first
one or two bites, but these days, he is vomiting approximately
once every week or two. And he doesn’t empty the
entire contents of his stomach. Daniel will try to make
the effort to keep it down. He also has started to take
some normal food like scrambled eggs, pasta, Chinese
noodles, hamburger, and fries. And we no longer have
to give him his milk asleep – he is drinking it
from a special cut-out cup that we feed to him.
Daniel started out in the 10th percentile for weight
and was quickly dropping as we started the LAFC. The
doctors were talking about the possibility of Daniel
getting a GI tube. Now he is a little below the 50th
percentile for weight and never required the feeding
tube. He still has some areas to work on though, like
taking more textured foods and weaning him off the baby
jars. Our insurance did not cover it although others
do, but it was truly worth the expense. It is some of
the best money we have EVER spent.
I also know of another family with 6 yr old cystic fibrosis
(CF) twins who are classmates with my older child. They
were taking most or all of their food through the tube.
One of the twins is ready to come off the tube through
the work that Ben has done at the LAFC, and the other
who did not eat any food orally before is making significant
progress.
Best of luck,
Eileen Shih
Vlada---- Mother to Julia (8 months old)
My baby girl who nursed so well in the first month of
her life stopped eating when she was 6 weeks old. She
could go without eating for up to 11 hours (which is
not OK for a 6 weeks old baby). She would not nurse
or take a bottle except when asleep. Even when asleep
it was a challenge: it would take her 3 hours to finish
a 3oz of milk or formula. By the time she finished it
was time to feed her again; we were constantly feeding
her.
She was diagnosed with reflux and was prescribed Zantac,
which helped very little. She was still eating slowly
and showing no interest in food. Because she was refusing
to nurse or take a bottle for long hours, we started
using a dropper or a spoon to feed her. The spillage
was high and she would vomit once in while. We went
to see a regular hospital feeding therapist who encourages
us to continue distracting her attention by showing
her toys or TV. We did not even go for a follow up visit
because these methods were not effective. Our daughter’s
weight gain slowed and I was extremely scared for our
baby’s health and development.
I hoped in vain that she would eat better with solids.
It would take us an hour to an hour and a half to feed
her one meal. She would hold food in her mouth and swallow
only if we gave her a pacifier. She eventually developed
a dependency on the pacifier to trigger her swallowing.
Toys and TV were effective distractions only in a short
term.
Then, a couple of months ago I heard about the Los Altos
Feeding clinic and Ben Zimmerman who does miracles with
babies and kids: THEY START EATING! Kids who never ate
by themselves started eating at his clinic.
I cannot describe how much I appreciate what Ben did
for us. It was hard to change our behavior during feedings,
to pay attention to our own reactions and responses
to the baby. But the results have been overwhelmingly
successful and worth all the hard work.
Ben showed us techniques that we had never heard of
or been shown before. After only one week of feeding
her and learning her habits, Ben was able to teach us
how to stop using distractions during her meals. We
adopted Ben’s protocol on a gradual basis, and
brought our daughter’s caregivers into the process
on an equally gradual basis. This has worked very well
for both baby and adults, and will continue to bear
fruit during the coming months.
We know our daughter will continue to improve if we
stick with the program – and this is the best
program we have seen! I would unreservedly recommend
Ben’s feeding clinic to any parent whose baby
has feeding issues.
Marion--- mother to Luke (4 years old)
I am the mother of a four year old little boy that ate
normally solid foods from a spoon up to the time he
was fifteen months old, which was exactly the moment
his brother was born. Subsequently, he would only take
the bottle and refused solid food. The bottles were
like a smoothie, filled with protein, carbs, vegetables
and fruits. We went to a food clinic within a hospital,
went to many different therapists and consultants, to
no avail. Prior to starting the program with Ben, my
son would drink eight to nine bottles a day and would
eat occasionally a yogurt, refusing any other solid
food.
The first session with Ben, my son was fed 8 oz. of
solid food with the spoon. We saw Ben approximately
for 3 1/2 weeks, mostly three times a week. My son is
now fed solid food with the spoon and drinks from an
open cup. He has three meals a day, no bottles, and
is rather happy to sit down and eat.
I am thrilled and overwhelmed with the success of Ben's
method. I wish I could tell all the parents out there
that have feeding difficulties with their children,
do not waste your time and money to go down the road
of therapies after therapies. Go to Ben, his method
works like a miracle. Some people may think it is hard
to go through it, but it really is not. It is in the
best interest of your child. Thank you Ben! May many
parents benefit from your knowledge.
Marion
Sumaya----Mother
to Rimaan (5 months old, only eats in sleep)
Our
son had severe food refusal/oral aversion when he was
5 months old. He would absolutely refuse to take his
milk. He would go 17 hours without getting hungry and
we would feed him using dropper.
His
weight was steadily dropping, so we had to take great
pains to make sure he gets something. It would take
1 to 2 hrs to feed him just 4 ounces of milk in his
sleep and all we would do in a typical day is feed him.
He
required a lot of toys and distractions. Sometimes he
required to be put asleep for his milk feedings which
also was quite impossible as he was deep sleeper and
would stop sucking after 1 or 2 ounces.
And
after all this effort, he would throw up. Things were
quite difficult with a lot of cleaning up of his throw-up.
He would always gag and throw up whatever was fed. We
had to literally force feed him to make sure he got
the bare minimum. This was becoming increasing stressful
on me and my husband that we both had to take time off
from work to take care of our son.
We
also tried solids on him which was even more disastrous,
as he would throw up the milk he had in the previous
feeding. We were not even successful in getting him
to take even 1 small spoonful of food. Because of the
stress, my health was getting impacted too.
After
hearing about success stories about Los
Altos Feeding Clinic from numerous feeding support
groups and our GI specialist, who was familiar with
the clinic, gave us a referral to Los
Altos Feeding Clinic.
Within
the first week, we could see difference in our son’s
mealtime behavior. The feeding therapist Ben Zimmerman
confirmed Rimaan's problem as behavioral. The therapist
used a certain behavioral approach to feed Rimana. The
treatment had its course of 4 weeks with 3 visits per
week.
Rimaan's
food intake improved dramatically after the 2nd week.
I could get my son to open his mouth and eat. Because
of consuming solid food, his liquid intake improved.
Now my son eats very nutritious foods because of which
he has gained a few pounds. From 5th percentile, he
is now in the 50th percentile.
Previously
he would throw up at least 4 times a day his complete
feeding and now it is just once a day. This program
has certainly worked for us so far. This has been
our miracle.
We
extend our grateful thanks to Los
Altos Feeding Clinic for helping us out and restoring
normalcy in our lives. Now I can do other fun things
with my son besides just feeding him. The support system,
resources, and information from Los
Altos Feeding clinic is excellent and helped
us through this ordeal.
Kristin---Mother
of Allyson (repaired cleft lip/palate and ectodermal
dysplasia)
Allyson
is 2 ½ years old and has been fed through
a g-tube since she was 3 months old because she
was aspirating and classified as “failure
to thrive”. It was determined that she
had an “underdeveloped swallow” and
couldn’t coordinate her “breathe, suck,
swallow” properly because of her cleft palate. She
also has reflux and delayed gastric emptying. For
most of her life, Allyson has been fed through her
g-tube via a pump at a relatively slow rate. Allyson
is also affected with ectodermal dysplasia. This
condition is characterized by poorly formed teeth,
many missing teeth (her only tooth on the bottom
is a molar), dry mouth and minimal saliva, and a
small jaw/large tongue.
At
nine months old, Allyson was cleared to try pureed
food, but we were “warned” not to push
food on her too much until her cleft palate was
repaired (at thirteen months). Several doctors
and therapists told us that “she would eat”
once her cleft palate was repaired and the g-tube
would be gone a few months later. I assumed
they were right and that she’d eat once she
was anatomically “fixed.” No one
told us HOW to make her eat. So we tried and
offered and waited and tried and offered and waited. We’ve
worked with two OTs and a SLP for approximately
15 hours/month for the past year and half –
that’s 270 hours of professional expertise! During
that time, Allyson was 100% medically safe to eat
and never had any oral aversions or defensiveness. Her
reflux and delayed emptying were under control with
medication (Reglan, Zantac, Prevacid). She
tried a variety of foods and seemed to enjoy eating,
but would never eat enough by mouth to sustain her
caloric needs. At 2 ½, Allyson also
no longer sat still to eat, so she often ate while
being chased around the house with a spoon. After
all of our efforts, Allyson was still being feed
50% through her g-tube - I was desperate for help!
I
found this website earlier this year when I was
frustrated about Allyson’s apparent enjoyment
in eating, but unwillingness to do so consistently. We
had gone through too many rounds of “one step
forward, two steps back” and I was determined
to find a program to move us forward and help us
reach our goal of being “g-tube free by three”! We
had an evaluation with Ben in the spring and he
told us that he could have Allyson off the g-tube
in 4-6 weeks. Yes, I was skeptical, but I was
willing to try his behavioral approach and help
her learn to eat by mouth. On our second day
at the clinic, Ben was able to feed Allyson enough
pureed food by mouth that I didn’t have to
feed her through the g-tube that night. It
was the first time in 27 months and 5 days that
she wasn’t hooked up to her feeding pump at
bedtime! That was over 6 weeks ago and we haven’t
looked back! Now I’m feeding Allyson
using the protocols we learned at the clinic and
she consistently eats 6-7 ounces of purred food
and drinks 4-5 ounces of formula or milk at each
meal. She’s also taking just one Prevacid/day
and has been weaned off all her other medications.
Ben
is able to help any child to eat as long as they’re
medically safe to do so. Allyson had many cards
stacked against her when it came to eating by mouth
– g-tube dependent for over 2 years, cleft
palate, missing teeth, lack of saliva, a large,
uncoordinated tongue in a smaller-than-average jaw
- and she’s now eating! It’s a
huge commitment and a lot of hard work, but the
end result is priceless. We spent just 5 weeks
at the clinic working with Ben and he’s changed
our lives forever… he can change yours too!
Nicole---Mother
of Greg (4 year old with severe autism)
Our
son was almost 5 years old when he entered the Los Altos
feeding clinic. Greg had feeding problems all his life
and for over a year had refused all solid food. He never
had medical problems; however, he is autistic and sensory
issues arising from autism caused a strong aversion
to putting anything in his mouth.
We
tried several years of feeding therapy in our home town
with no success. Our insurance recommended a hospital
based feeding program but they were unwilling to treat
our son due to behaviors related to his autism.
Fortunately
we found Ben Zimmerman at the Los Altos feeding clinic.
Ben's feeding method broke down our son's aversion to
food in just a few days, and soon he was taking baby
food willingly. The program trained us to feed our son
properly in different locations. We went home after
just 3 weeks.
We
were worried about our son continuing to eat after going
home where there was a long history of food refusal,
but the feeding program was so solid that our son had
few problems. In fact, he now asks to eat when he is
hungry. We are thrilled with the results of this feeding
program.
Ellie---mom
to Sava (17 months)
Our son, Sava, came to the Los Altos feeding clinic
when he was almost sixteen months old. At that point,
his weight had fallen off the charts and his height
was starting to slip as well.
As
an infant, Sava had bloody stools and moderate reflux,
which later got diagnosed as allergies to dairy and
soy; through food trials, we've determined that he is
allergic to several other foods as well. Sava breastfed
well and exclusively for the first six months, with
me on a strict dairy/soy free diet.
He
started becoming a distracted nurser when we started
to introduce solids, and by nine months he was nursing
so erratically that I was forced to switch over to pumping
in order to make sure that he drank the required amount
of breastmilk. I continued to pump--a full-time round-the-clock
job--until we came to the Los Altos feeding clinic,
since breastmilk was the only nutritious food Sava was
guaranteed to take on a regular basis.
We
started Sava on solids at six months, but he never took
to the spoon with enthusiasm; around nine months, he
stopped taking the spoon altogether, and we followed
the advice of pediatricians, as well as an occupational
therapist, not to push him. He self-fed from eight until
sixteen months, but because his diet was already limited
and he became increasingly picky, by sixteen months
he was eating very few foods, and he was not getting
enough calories. If we tried to give him anything from
a spoon, he would push us away and start crying and
fussing. To make things worse, because we were so desperate
to have him eat, we gradually helped him develop all
sorts of bad eating habits: breakfast only at the park
while playing, french fries almost every dinner, the
list goes on.
We
came to the Los Altos feeding clinic with one hope:
to help Sava learn to eat from a spoon and to convince
him to take in more, and more varied, calories; we also
hoped that I would be able to get off the pump, since
pumping had left me with no time to work or rest.
After
four weeks of therapy with Ben, and many emotional ups
and downs, we were able to take Sava home and to feed
him three 6 oz. solid meals a day. Instead of the three
or four foods that we had come to rely on as his main
staple, we can now feed him everything to which he is
not allergic. Meals last an average of fifteen minutes,
and we no longer worry that he is not getting enough
nutrients. Sava is still not the enthusiastic eater
that some children are born to be, but his behavior
during mealtimes is unrecognizable from what it was
six weeks ago. To say simply that Ben Zimmerman and
the Los Altos feeding clinic have been a blessing would
not convey the extent of our gratitude. Our lives have
been transformed.
Ann---mother
of Kathryn (12 months)
Katie
was born with a cleft palate and throat muscle palsy
which made it very difficult for her to drink.
At 8 months she underwent surgery to repair her cleft
which left her traumatized and unwilling to take a bottle
or sippy cup. She would only consume milk by spoon
and it was not enough to sustain her growth or cognitive
development. She had fallen off the charts in
height and weight despite us spending practically all
our time struggling to get her to eat. At the
Los Altos Feeding Clinic we were taught new feeding
protocols and how to prepare high calorie, nutritionally
dense food so now meal times are no longer a fight and
Katie's steadily gaining weight. As a result,
she’s climbed up to the 25th percentile in weight
and is still gaining.
Rachel---mom
of Scarlett (6 months)
My husband and I welcomed twins, a boy and a girl, born
at 33 weeks. After a few weeks as "feeders and growers"
in the NICU their ng tubes were removed and they came
home. Our daughter Scarlett never took the number of
bottles they wanted her to in the NICU and we were instructed
to feed her what she did not finish in a bottle via
a ng tube. We stopped this practice after one month
of being home with her. At this time she began spitting
up large volumes of her bottles and her disposition
at feedings went from lethargic to irritable and combative.
Everyone said she would "grow out of it" and "oh, you
have a reflux baby" and the most annoying, "she is probably
picking up on your stress, try to relax!" We did everything
we could to make feeding her relaxing: dimming the lights,
soft music, walking her around the block, swaddling
her, you name it. My mother in law sent me the web link
to Los Altos feeding clinic but I hoped she would grow
out of it. We struggled through life with our twins
at 3, 4, 5, and 6 months old with an unbearable weight
of stress, concern, worry and anguish. We took Scarlett
to a pediatric gi who dismissed our concerns. We consulted
with other pediatric gi specialists, many of whom suggested
the fundo surgery, which has a lifetime of side effects.
We tried every medication for reflux available. We met
with a speech therapist who did weekly weight checks
and encouraged us to get a feeding tube and "try to
bond with her in other ways". Scarlett was losing weight
and in the 5th percentile. In the whole month of May
she gained 2 ounces. Each day and night was a slow passing
of minutes and hours spent fruitlessly coaxing her to
eat. At 4 and 5 months some days she took in as little
as 13 ounces, the highest was 24 ounces. It could take
30 minutes to feed her 1 ounce and we usually had to
feed her when she was asleep because she would scream
like we were killing her when we fed her when she was
awake. My husband and I were juggling careers, twins
and serious concerns about our daughter's health. I
gave up hope that she would "grow out of it" but did
not want to subject her to surgery with its side effects
and likely consequences of demanding a feeding tube.
The final straw came when we tried to feed her solids.
She vomited literally everything and every time we fed
her. We tried that for weeks and finally gave up and
consulted with Ben.
At
6 months of age, Scarlett began his program. We had
to leave our home, friends, family and our jobs (in
Texas) to fly to CA
and move into a hotel to do the program. Of course,
I'm not including paying for the program! But it had
reached a point in our lives where it was no longer
bearable or tolerable. Within a few days Ben had eliminated
Scarlett's gag reflex completely and she was eating
close to 2 ounces. Encouraged by the gains we saw in
the first week, we started the second week with optimism,
only to have her progress slide back and plateau. Luckily,
she improved somewhat the last week. Ben told me at
one of her first feedings a case like Scarlett he'd
like to ideally work with for 6 months. If I lived in
Sunnyvale CA, that
would certainly be possible, but I didn't and we could
only afford three weeks of his program. It would have
been easy for Ben to tell us he had done the best he
could, he needed more time, etc but his number one goal,
which was reflected in everything he did and said, was
to ensure feeding times were a managaeable as possible
for us as parents. While the whole experience of particating
in the program can feel surreal and scary at times,
Ben is an exceptionally caring, thoughtful, and considerate
individual who takes every available moment to check
in with you as parents and support you and your child
through the process. Scarlett is a heathly, thriving,
9 month old who JUST landed on the growth chart. While
she is still a "fussy" eater and by no means a chubby
baby (she is now in the 5th percentile for growth) she
does not vomit copious amounts everyday, usually only
spits up a few times a week and takes in more calories
each day than her brother, thanks to us making a very
high calorie food concoction Ben trained us to prepare.
Luckily the high powered blender we use to prepare her
food also makes sublime margaritas and with Ben's support
and feedback on our adventures in feeding our child
and her progress, we're making it. Since coming home
with her we've seen a decrease in the amount of crying
normally associated with mealtimes and we look forward
to a future of happy, heathly eating.
Since
taking Scarlett to the feeding clinic her entire disposition
has changed completely. She used to be an irritable,
fussy temperamental baby. She is now a funny, joyous,silly
giggly baby. Scarlett was only 6 months old when we
brought her to Ben and we realize our experience isn't
typical of many of his clients since our child was so
young and we had a limited frame of time (3 weeks intensive
to see him). However her progress, despite it's slow
pace, has been significant and rewarding and I could
not recommend Ben more. His patience, understanding,
confidence and and compassion is a godsend to parents
desperate and out of answers or (like us) getting all
the wrong answers.
Emma---mom
of Sheldon (10 months) and Rozanna (7 years)
Both of my two children received treatment at Los Altos
Feeding Clinic. Rozanna was born full term and never
had any medical problems. For a reason we may never
know, she lost interest towards feeding around 3 months
of age. I had to stop breastfeeding and pump, adding
formula to breast milk in a bottle to increase calories.
She didn’t care much for the bottle, even when
she should have been very hungry. It was so strange
that a child would not want to eat. Things did not get
better with introduction of solids. She’d only
eat crunchy foods that did not smear on her hands or
in & around her mouth, such as a fresh cucumber,
celery, watermelon. After a while, she got used to Pediasure
from a bottle. Her weight, even though growing little
by little, remained under the curve, and I did not have
peace being unable to make my child eat better. Years
of weekly OT sessions at Stanford and Children’s
Health Council, consultations with a psychologist and
psychiatrist, did not produce significant results. At
7 years of age, I still had to feed my daughter in order
to get sufficient amount of calories in, and she took
a very long time to chew her food.
It took only a few sessions with Ben Zimmerman, to change
my daughter’s behavior around meal times. For
the first time ever, she eats by herself, finishes her
meals in under 20 min., and her weight is on the chart!
She has more energy, independence, and self esteem.
I wish we met Ben back when Rozanna was a baby. It would
have saved us a lot of worries and frustrations, and
helped Rozanna grow stronger and happier.
In
2006, my second child was born, and I really hoped he
would be a good eater. And he was, but only at nursing.
When time came to introduce solids, we had problems
with not swallowing food but simply spitting it out,
bite after bite. Frequent vomiting was later attributed
to reflux and managed with medication, but swallowing
problems continued. The weight curve was flat and got
further from the curve as time went by. Because my baby
was healthy otherwise, the pediatrician referred us
to Los Altos Feeding Clinic. Sheldon was 10 months old
when we started therapy. I was able to watch the sessions
from the waiting room and was impressed by Ben’s
patience and ability to find an approach that was just
right for my child. In a couple of weeks, my baby was
eating from a spoon, and I was soon trained to feed
him myself. Within weeks, Sheldon’s weight curved
upward, crossed the bottom percentile, and continues
to grow at a steady speed.
After achieving stable progress with solids, we’re
back at the clinic to learn to drink from a cup. (I
guess I missed the “window of opportunity”
to introduce a bottle early on, and so Sheldon refuses
anything but breast for his liquid intake.) After just
1 week of treatment, there’s no crying or resistance
to the cup, the clothes are clean and dry, and I can
really see the progress in Sheldon’s acquiring
a new skill. Every time he comes out of the treatment
room after a session, I see a smile on his face. What
a difference a full stomach makes! My kids also enjoy
the time before/after sessions when Ben plays with them.
He’s a pleasure to know.
I’d
like to point out that, unlike most children who experience
feeding difficulties, my kids were born healthy full
term babies. And if not for the help we got from Ben,
they might not grow up to be so healthy and happy. I
highly recommend Mr. Ben Zimmerman at Los Altos Feeding
Clinic to anyone struggling to feed their child.
Barbara, mother of Ben (3-years-old)
My son's feeding aversion started when he was 2-years-old. The food he was eating consisted of applesauce, yogurt, smoothies and crackers. During his 2 year check up with the pediatrician I addressed my concerns about his limited food intake. The doctor explained that there was no reason for concern adn this was just a "picky" phase which he would grow out of.
At the same time, my son was being tested for delayed speech and needed to start speech therapy once at week. I learned from the initial evaluation and his assigned speech goal was to strengthen his weak jaw muscles and this would eventually help with his feeding aversions. As the year progressed my son's speech started to improve a little but his feedin gaversion and food intake got worse. As a result, I spent hundreds of dollars on any and every book on eating habits for toddlers and continued with no success.
By his 3rd birthdayhe was only eating cereal, applesauce, crackers...and sometimes a smoothie. His ribs were starting to show and his tall body was getting too thin. This time at my son's yearly check up our pediatrician said not to worry and to start presenting meals with no snacks in between and eventually he will eat. The doctor warned us that my son might not eat for a day but will be too hungry to resist the meals the followeing day. So I went home determined for this plan to work. My son did starve himself for two days and the third day he woke up throwing up clear liquid with bile shortly followed by spells of dry heaving. Then the rest of the day he spent on the couch trying to get his strength and color back. I thought it was a virus he was fighting until it became a pattern.
Once again, I met with our pediatrician about these recent developments and he recommended some tests to be done. The results showed there was no organ damage and all the blood tests came out fine. The next step was to get an upper GI test but after my son and I returned from a family vacation, I was exhausted and frustrated with having no plan and on what to do with my son getting thinner and refusing to eat.
Another reason for my exhaustion was going through the past year with my son's challenging behavior. I was not able to communicate well with my son due to his delayed speech as well as my son's hunger lead to many lengthy tantrums.
So I started to do my own research on the computer. I believed there had to be a place, hospital, or clinic that could help with this type of problem. The advice from others was driving me crazy because it all started with, "oh, it sounds like you have a picky eater. Don't worry he will grow out of it."
Luckily, I found a place called the Los Altos Feeding Clinic. I picked up the phone immediately and called Mr. Zimmerman. After looking over his website and reading his background I started to finally feel some glimmer of hope. To be honest, I was counting down to days till our evaluation with Mr. Zimmerman.
After our initial meeting with Mr. Zimmerman I believed we were at the right place. He discussed what the treatment program would entail and gave me a list of famillies who had graduated from the clinic. He explained that not all kids are the same, therefore, each treatment program is different and esigned for your child. Furthermore, I was told that Ben would eventually be eating various meats, seafood, vegetables, and fruits. I laughed a little when he said this because it sounded too good to be true. I went hom that night feeling our family finally had some direction. I knew it would be a hard process but our only choice was to go forward. We started treatment that week, and we called the list of families who went through the program. I enjoed all the conversations and it was confirmed that each child is different in age, health, and development but all have similar eating problems and most of all, all families felt the same frustration and exhaustion before attending the Los Altos Feeding Clinic.
After 6 weeks, my son is now 40 pounds, and in the 95th percentile for his weight and height. He is eating more than 150 different types of food ranging from tuna, slamon, broccoli, lettuce, steak, mango and even crab claw (which he loves!).
I do not wish any parent to go through their child not eating. It is a draining and emotional process. I am so thankful and forever grateful for Mr. Zimmerman helping our family by teaching my son to eat and as a result helping my son grow in height, weight, and spirit. My son's speech has drastically improved as well as his awareness and reasoning. I feel like my son is more active and alive.
Suyan, mother of Nina (1-year-old)
My daughter Nina was a full-term baby born at 6 pounds 7 ounces. The feeding was very smooth at the beginning, but it has become difficult since Nina started vomiting a lot at 2 months old. It took at least an hour to give her 5oz milk, and she would throw up almost half of it even under the control of Zantac. She was referred to a GI specialist when she was 6 months old due to the severe vomiting. Acid reflux and oral aversion were diagnosed then. However, the feeding continued getting worse. She totally refused to take a bottle when she was seven months old. She was not taking solid food, either. She was admitted to the hospital for detailed exams. Although every result came back normal, she was discharged with a NG-tube after the 11-day of hospitalization.
The nightmare had just begun…Nina hated her NG-tube. She tried to pull it out all the time, the tape on her face irritated her baby skin, and the vomiting didn’t stop. I took her to occupational feeding therapy near our home in Florida three times a week. I gave her lots of smiles and praise when she occasionally took a bite. However, for the most of time, she was just turning her head away from the spoon. After she was on the NG-tube for one month, the doctor suggested us to consider a G-tube, which we would like to avoid. I started looking for the information regarding feeding programs. I talked to Mr. Ben Zimmerman at the beginning of December. After three weeks, we were at the Los Altos Feeding Clinic.
Nina’s tube was out by the third day of therapy. After a 7-week treatment, Nina was taking all her food and drink orally, and had gained 2.5 pounds. We came back to the clinic for another 2 weeks to train my husband as a backup feeder (mom needs a break…). We ended up with an easier protocol because Nina’s eating skills had improved over the past two months. Now, she is taking 400-500 calories per meal, three meals a day. Each meal takes 20 minutes. The best of all, she barely throws up!!! I guess the stomach is not meant to receive food directly…
Nina just turned one last week. She looked so cute without the tube on her birthday pictures. Thank you, Ben, from the bottom of my heart.
Los Altos Feeding Clinic
2235 Grant Rd. Ste 2
Los Altos, California 94024 |