Bear fight with spinocerebellar ataxia 7

Spinocerebellar Ataxia type 7(SCA7)Is a genetic progressive disease that attacks the cerebellum and the brain stem. I'm sure most are unfamiliar with this, as it is a extremely rare genetic disease affecting only 1:100,000 in the population, his specific type, type 7, affecting 2% of all SCA's (spinocerebellar ataxia) as there are multiple types. There is no cure and no treatment. No drug, shot, pill, or routine can stop it. It attacks the body and causes multiple organ failures. Blindness, dysphasia, vomiting, ataxia, convulsions, heart failure, kidney failure. The list goes on.

After waiting for what felt like days Our sons MRI was abnormal. His brain showed cerebellum atrophy. They ordered a number of genetic tests. We were told to just make memories. And that he would gradually get worse.

Jeremiah was admitted into the hospital Saturday. Numerous test have been ran but no answers have been found.

His dad and I have not been able to work due to him being hospitalized. Please continue to keep my family in your prayers as we go through this heart breaking journey. Whatever donation is greatly appreciated.