At three months old Jesse was put into the hospital because he wasn't eating well and had lost so much weight. He was in the hospital for a week and at that point it was discovered that his jaw and tongue were not coordinating together to eat. The week Jesse was in the hospital he had many blood tests, an EKG and a head scan.
For months now Jesse has had eating therapy along with physical therapy twice a week. He's going to be a year old on October 22nd and he isn't sitting on his own, he's not crawling or walking, has stigmatisms in both eyes and has to wear glasses.
The first of August Jesse had an MRI and the Doctor discovered that the white matter in his brain is under developed. So we are hopeful that as he grows the white matter will continue to develope.
Jesse then had to have an upper GI test, which he had to drink a dye so the Doctor could see if everything flowed through like it was supposed to, which it did. Once they knew everything was ok, Jesse was scheduled to have a feeding tube put in on September 1st.
After three months of having the first feeding tube Jesse will have to have a different tube put in and will have to go back through the same surgery again.
On October 10th Jesse had genetic testing done and depending on the results of these tests he may have to have more extensive testing done.
My Son Jeremy Ogle has insurance through his work but it doesn't cover all of Jesse's medical expenses along with the feeding tube supplies which is causing a huge financial strain on the family.
Please keep the prayers coming and any donations would be greatly appreciated.
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