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Old 05-07-2012, 02:48 PM
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HalcyonDays HalcyonDays is offline
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Join Date: May 2012
Location: Oklahoma City, OK
Posts: 5
10 yr Member
HalcyonDays HalcyonDays is offline
New Member
HalcyonDays's Avatar
 
Join Date: May 2012
Location: Oklahoma City, OK
Posts: 5
10 yr Member
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OK! Seems like I've seen a few posts since I've been on last. I'll try and answer what questions I saw.

In regards to my ability to work, I actually can work, albeit I absolutely must have pain medication to manage my CIPN, or I'm reduced to a shambling wreck. Standing for any length of time makes it worse, as the nerves in my legs are probably nothing what they used to be, especially my left leg. The pain is always in the same region, right below my knees to just above my ankles. The fact that I can work was another reason I was skeptical of being able to qualify for SSDI or SSI, because as Teatime put it, I can work a job for more than 4 hours at a time. Granted it has to be a sit-down position or it causes me extreme pain if I'm on my feet for any length of time.

The big mystery to me though is my CIPN pain only really started to manifest in a significant way almost a decade after my initial chemotherapy exposure. It was when I was 18 that I really started to notice the pain, and I initially was diagnosed with a severe case of Restless Legs Syndrome, but after more testing the diagnosis was changed to severe CIPN. The pain has steadily increased ever since, and its constant, 24 hours a day, 7 days a week, without pain medication. I honestly don't know why it has only started to become worse as I've gotten older, CIPN I don't think is even fully understood by my doctors, and even less by me personally.

All of the talk of me getting on SSDI/SSI was external, I never came up with the idea myself. That's why I'm here, because it confused me that I felt I was able to continue working as long as I had a pain management system set up (currently I'm on Tramadol 50MG every 6 hours, which I pay for by doing commission artwork), but had several people, including a social worker from St. Judes telling me I should try to get it. My confusion over SSI/SSDI was that everyone always kept referring it as SSI, I always assumed they were the same, but you know what they say about assumptions I suppose. I have been offered a follow up study at St. Judes for adult patients that will provide me with paperwork that has been proven to assist former patients in getting their disability cases won, so I might look into that at some point if this persists.

I'll do some more research.

~HD
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