My concern is when will SSDI run out of funds. A person at the SSA office tells me some people can have a lifetime of benefits while others, they can be very strict with depending on each individual medical condition. As I told the person I am fine until I may accidently not knowing MSG, CARRAGEENAN or some other food toxins may create a seizure if I would eat a food with those things in them. I asked her of all SSDI cases if there were some people besides me that were disabled because of a reaction to food chemicals and she said there were but she never knew food chemicals could cause seizures. I was able to get my SSDI 2 years after my brain surgery. If I never had my surgery odds were I would never have won in 2003 after my 3rd try, as I had to get a SSDI lawyer to win it on his 1st try with me. I was able to get money retroactive from the first time I tried on my own in 2001 before my surgery. You may want to get
a lawyer who only handle SSDI cases and nothing else if you can't win it on your own. It's all part of the judicial system that a lawyer has to have part of what is ours. The worst part about it is the lawyers will tell the judge the same words you would tell them, as no different condition would be better or worse for most of us, besides maybe more auras or seizures judges would cause, by making us get a lawyer to win.
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