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We had SSI for Ryan early on in his diagnosis. The social workers at the hospital were crucial in helping us get it. Also, you need to discuss the extreme need for it with the doctors because they can word the paperwork so that it makes things sound more disabling. We stopped getting SSI because we needed the Medicaid health insurance more than the money and the SSI was putting us causing them to cancel that. Your travel expenses should be deductible on your taxes at the end of the year as a medical expense. After 6 years of us traveling an hour back and forth for pheresis/infusions, at one point daily, we are now blessed and the local hospital does Ryan's infusions. It's about 8 minutes from my house. He no longer has Medicaid and we have to fight with a regular insurance company alot more. I didn't work for the first 3 years of his diagnosis, but now I am back full time. For a bit I sold Avon to friends and family for some extra cash. It was pretty easy and if you sold enough you got 50% profit. Hang in there and things will get better. It was rough for a while but now it's not as hard and I'm lucky enough to have an understanding employer when we do end up in the hospital.
Permalink Reply by Colette Ann Frysz on August 20, 2009 at 8:50am
Permalink Reply by KaTrina Slaughter on September 17, 2009 at 2:06pm WELCOME - Friends, Family Members, Patients, and Researchers - JOIN US!
The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this rare complement disorder. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome.
Sharing information, inspiration and support for one another, we seek to gather together people and knowledge as we strive to improve the lives of patients and families dealing with a diagnosis of aHUS.
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