I can see the halfway point in the distance, and I am so
glad we still have so much time!! Gavin
has come so far, and I know he will continue to improve with each day. Feeding struggles are long journeys and I
have begun to realize that sometimes you just have to wait until your child is
ready to eat. Gavin spent two years in
therapy just playing with food and exploring different textures. It was frustrating at the time to not see
progress with eating, but I see now how important that time was. He was able to overcome so many sensory
issues that prepared him for eating…kind of like prerequisites. I truly believe he would not have been as successful
with chewing and swallowing had we not gone through this therapy. Gavin is finally old enough and smart enough
to understand the concept of eating!! He
asks for snacks all the time nowJ. He wants to eat so badly, and it is so
amazing to see him finally be able to eat some foods without choking and
gagging!! I also think this program is
amazing for kids with NDI. There is
nothing physical that is preventing Gavin from eating, he just needs to be
taught those important skills of chewing and moving his tongue that he never got
the chance to develop. The water does
still make it a little tricky, and no matter how much progress I want to make
with food, water has to be my first concern.
Gavin has been practicing chewing more. I cut up an apple today for him to chew in
the mesh, and that seemed to go a little better than the toddler apples we
tried yesterday. Gavin kept asking for
an apple as I put him to bedJ. If I weren’t exhausted, I would have taken
him downstairs to get one!! Gavin also
chewed peaches in one of his meals and loved them. He even asked for more!! I made some chicken and rice with some
vegetables from my low sodium cookbook last night that they pureed at the
clinic today, and Gavin did great with it.
It is so nice to see him eating food that I know we would eat in our
house…even if it is pureed. We discussed
eliminating PediaSure from Gavin’s diet, and everyone is on board!! Since he is able to eat foods to satisfy all
of his dietary needs, we will switch to whole milk and V8 Fusion, making sure
we bump up the calories as needed. I am
so excited to not have to smell that nasty PediaSure anymore!!
Gavin has started self-feeding during the meals!! He is using kind of a fancy spoon with two
bends in the handle. The spoon will be
loaded up for him, and he is instructed, with some assistance at first, to
raise up his elbow as he brings the spoon to his mouth. Gavin LOVES his independence, so he has
caught on real quick! I now see hope
that not only is there going to be a day that Gavin eats solid food, but that
he will be able to feed himself as wellJ.
We got a card in the mail from Gavin’s “school”
Primrose! I read him what each of his
teachers wrote and he smiled and giggled at each oneJ. We miss you all at Primrose and cannot wait
to come home!! I know Gavin will miss
his tubing time up front, especially with Ms. Nash, but I’m sure you can bond
with him during gym time…he randomly mentioned again that he does not like
gym!! He gave me a very elaborate reenactment
of someone rescuing him from gym class…you would have thought it happened just
yesterday!! Thank you Ms. Long for all
of you support and encouragement as we’ve been here! Our little eater will be back before you know
it!!
Sandy: Your blog will be so encouraging to all parents, who have been going through "eating" disorders. So happy you have bonded with those other mothers; I'm sure you give comfort to each other. You are an amazing Mom, who fought through so many obstacles to get you and Gavin exactly where you needed to be! One day at a time……….thinking of you - Eileen
ReplyDeleteHi Sandy,
ReplyDeleteI am just now catching up on the week. I've had a busy busy week! I am so glad you received the card. We miss that sweetheart! I am so glad things are going well. Think of you all often, and I can't wait to hug Gavin!
Love, hugs and prayers,
Kandi Long