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Testimonials:
What
our clients are saying about the Los Altos feeding Clinic.
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.
Kathleen
----mother to Kristen (7 years old)
My daughter Kristen was born in March of 2000 with congenital
Hydrocephalus, and as a result of elevated intracranial
pressure in utero, she suffered an ischemic episode
and developed hemiplegic cerebral palsy, severe visual
problems, epilepsy, and developmental delay.
Kristen had her first shunt placed when she was 2 days
old. She was sent home at 6 lbs, with a nasogastric
feeding tube in place and instructions to feed her through
the tube whatever she couldn't finish through the bottle.
After her 4th neurosurgery at 7 months old, she was
still barely 12 lbs. It was suggested that I stop attempting
to breast feed and the NG tube was re-inserted, this
time it was in for nine months. Because Kristen could
not handle the volume, she developed severe reflux,
even though we were extremely careful to run the pump
very slowly. We would think she was okay, then before
we knew it she would be throwing up across the room,
choking, and turning blue. The feeding tube that went
in through her nose would come up out of her stomach
and out of her mouth, and I would need to leap across
the room and pull it out. And if that wasn't awful enough,
I would then have to re-insert it. Over and over again.
We were referred to a local feeding therapist when Kristen
was almost a year old, whose evaluation stated that
her "oral-motor components are intact and adequate
for the management of liquids from a bottle and pureed
foods from a utensil other than a spoon. At this time
Kristen has an oral aversion to the spoon and when it
approaches she closes her mouth and turns away. She
seems, however, to enjoy the taste and texture of the
food that is offered to her either by finger or by dropper."
At this time, I began to feed Kristen with a 1 ml dropper,
because of her "oral aversion to the spoon".
As you can imagine, it was an extraordinarily time-consuming
process. I continued to do so until some other well-meaning
therapists said that I shouldn't try to feed her when
she didn't want to eat and suggested that we go back
to feeding her with a bottle until she "wants to
eat". By this time, I had managed to get her into
the 5-10th percentile on the growth charts, and her
"failure to thrive" diagnosis was considered
resolved.
Time passed, Kristen was almost 3 years old, and ready
to enter the school system. Her main nourishment was
still Pediasure from a bottle. No one knew what to do
about her feeding situation. I knew she wasn't getting
enough, but I didn't want her to have a feeding tube
placed because if an infection were to occur in the
G-tube site, it could travel to her other shunt endings
and end up infecting them, which could have deadly consequences.
We prayed and prayed that every year, she would somehow
"start eating". How that was supposed to happen
was a mystery to all, as she was still turning away
from the spoon. She underwent her 8th neurosurgery for
shunt malfunction when she was 3 1/2. She remained on
Pediasure in a bottle for the next 3 years, when we
re-initiated feeding therapy with the same therapist.
By this time, Kristen had fallen off of the height chart,
and was barely on the weight chart. We were given almost
the same advice from the feeding therapist as we had
the first time. The doctors said her intake needed to
be at least 1400 cals per day, but when we began trying
to give her that much she fought even more. When the
school nurse contacted me and said there was a problem
with "restraining" Kristen at school so she
would eat, I felt that I had reached the end of my rope.
Maybe I would need to pull Kristen out of school so
I could feed her at home all day so she would be able
to get the appropriate amount of calories the doctors
recommended. I wondered if anyone knew what a nightmare
we were going through, and how almost the only thing
I could think about from the moment I got up in the
morning until the time I went to bed at night was the
amount of food/Pediasure/calories that Kristen had consumed
for the day and if it had "been enough". Of
course I knew that most of the time it hadn't, and the
anxiety it produced was almost unbearable. There seemed
to be no place to turn.
I went online and searched again for help. This time,
the Los Altos Feeding Clinic came up, and I read and
read all of the success storied and testimonials of
children that Ben had helped to eat. It seemed almost
too good to be true. I called that afternoon and spoke
with Ben, who listened carefully and was optimistic
about Kristen's abilities.
We went in for an evaluation a few days later, and showed
Ben how Kristen wouldn't eat. He said it was a pretty
"straightforward case" and we almost fell
over. We made an appointment for the following morning.
The next morning, Ben was able to get 9oz. of thick
pureed baby food in Kristen in 15 minutes. We continued
for 3 sessions per week for about 2 1/2 to 3 weeks,
and then I learned how to feed Kristen. After 7 years,
Kristen's caloric intake is now up to over 1400 calories
per day of thick pureed food, she is being fed entirely
by a spoon and a cup from the front, each meal averages
less that 15 minutes, and she is completely off of Pediasure
and the bottle. We look forward to continuing to work
with Ben to upgrade the texture of Kristen's food and
to facilitating her to self feed as well.
To this day, I don't understand why this help was so
hard to find. Did I mention that I am an occupational
therapist? Did I mention that I have had access to the
"best of the best" as far as feeding therapists
are concerned, both on the web as well as through the
continuing education that I have access to as a healthcare
professional? I have read book after book, article after
article, on sensory integration theories, occupational
therapy intervention, adaptive feeding techniques, gastroesophageal
motility issues, etc., etc., etc. In looking back, I
realize that these behavioral techniques could have
been employed with Kristen following that initial feeding
evaluation, when Kristen was less than a year old. Why
did it take over 6 more years?
We remain profoundly thankful to Ben Zimmerman and the
Los Altos Feeding Clinic for the therapy that we feel
"saved our lives". If that sounds somewhat
extreme, consider the psychosocial ramifications of
being out in public with a 15 year old drinking a bottle.
Every piece of literature that I researched stated that
feeding problems do not get better, they get worse with
time. And the insertion of a feeding tube into Kristen's
stomach had the potential of deadly ramifications. But
even in my training as an occupational therapist, feeding
tubes are seen as "necessary" and "beneficial"
when a child refuses to eat. The risks, the strain on
the family, and the daily stress of the care of a child
with a feeding tube are something no doctor or therapist
can begin to explain.
Thanks Ben, more than you will ever know.
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
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.
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.
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.
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.
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.
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.”
Los Altos Feeding Clinic
2235 Grant Rd. Ste 2
Los Altos, California 94024 |
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