I applied for disability after working for 20 years with USDA. My last day was July 7, 2006. I did fine with the transplant working, but dialysis just made me too tired to do a "good" job and If I can't do a good job I don't want to be there. I may rent out Bounce Houses (Jumpie houses and the kids call them) when I move to Spokane. If I ever sell this frick'en house!
Somebody (stauffenberg, maybe?) posted that only about 30% of dialysis patients are able to work. I'm curious to see if that is true for IHD members.
Since most CKD/dialysis patients who have insurance, have it through their employer, why don't the medical professionals, especially the dialysis centers, do more to help patients feel well enough to work?
Quote from: Black on September 09, 2006, 01:23:44 PMSince most CKD/dialysis patients who have insurance, have it through their employer, why don't the medical professionals, especially the dialysis centers, do more to help patients feel well enough to work?Very good question. Joe's been dealing with RLS (like so many others here) and therefore not getting much sleep and that definitely affects his work, how many times he calls out, how well he performs while there, etc. Sometimes I feel like he's not taken seriously about his RLS.
Although I am on disability, I am a writer. Presently I am doing a series of books on maxamizing health, overccoming disease and fighting the effects of aging. I also have a series of health brochures that I distribute to Daycare centers. But don't tell the IRS. I'm a non profit organization Sassy
Angie, "Life Line 4 Your Health: A Journey". can be found on Amazon. However, if you wish to have a copy of a few I have written, no need to pay will be pleased to send them via internet email. to anyone interested. Just let me know. Sassy