Getting Amy to eat

Amy is sometimes hard to feed, she has always had trouble, its not her swallow its her chewing,Amy still has her g-tube in but we only use it for her seizure med's and sometimes liquid's.We now have a great chair that she sits in for meals, similar to the one she uses at school its great. This is Amy one morning before school reading her book waiting for her breakfast.Amy has come a long way in the feeding department, our next goal is to get her to feed herself for every meal.

H.U.G.S

Today is March 1st and we are going to have a HUGS meeting, that's (Hydrocephalus United Group Support) this support group was started four years ago by Margaret Woods and I, Margaret has a beautiful daughter named Abby who also has hydrocephalus and doing well, we would like to reach out to the hydrocephalus public and give all the support we can, we may not have all the answers but we sure can listen. Ill post pictures of the meeting in a later post.