Guest guest Posted October 29, 2002 Report Share Posted October 29, 2002 How would someone go about getting disability for pancreatitis? When do you know if it's severe enough? I've been off work almost 4 months this past year due to being ill with pancreatitis. Sphincter of Oddi dysfunction to be exact. I'm being treated at Mayo Clinic and my doctor has been great. My home doctor is also very supportive. Does anyone have any answers. My last attack (which I'm still off work for) caused my amylase to hit 1500 and my lipase was over 28000. The pain has been unrelenting, worse in the mornings after not taking pain meds for several hours I can hardly get out of bed or even sit up. Does anyone else have most of their pain located in their back? I've never submitted anything to one of these sites before. I'm 39, a non drinker, but have high triglycerides which they're treating. I guess that's all. Thanks for any help you have to offer. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2002 Report Share Posted October 31, 2002 > How would someone go about getting disability for pancreatitis? You can apply for social security disability benefits anytime. Either go to the social security website & download the application form or get a form from your local social security office. Be sure you answer all the questions. Don't be " macho " & minimize anything. Give full details about how your life is affected by your condition. Your doctors will be contacted; your medical records from doctors, hospitals, etc. will be examined. It sounds formidable, but it is very much worth the work to do the best job possible in filling out the application. You must be disabled for 5 full calandar months in a row before you are entitled to benefits. For myself, the process went fairly easily. I had become increasingly unable to work & by August, 2001, was working approximately 2-5 hours per week, instead of the usual 32 hours. I applied for disability in January, 2002. In April, 2002, I was notified that I was elligible for benefits as of Jan., & started receiving monthly benefits as well as a check for retroactive benefits (Jan-March). They counted my being disabled as starting in August, 2001. >When do you know if it's severe enough? If you can't work because of pain or nausea or because you're taking pain-killers, its severe enough. > Does anyone else have most of their pain located in their back? Most of the time my flare-ups start as either nausea or as back pain, just below where the bra strap lies. Hope some of this is helpful. Please feel free to ask any questions which may arise. jang Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2002 Report Share Posted October 31, 2002 > How would someone go about getting disability for pancreatitis? You can apply for social security disability benefits anytime. Either go to the social security website & download the application form or get a form from your local social security office. Be sure you answer all the questions. Don't be " macho " & minimize anything. Give full details about how your life is affected by your condition. Your doctors will be contacted; your medical records from doctors, hospitals, etc. will be examined. It sounds formidable, but it is very much worth the work to do the best job possible in filling out the application. You must be disabled for 5 full calandar months in a row before you are entitled to benefits. For myself, the process went fairly easily. I had become increasingly unable to work & by August, 2001, was working approximately 2-5 hours per week, instead of the usual 32 hours. I applied for disability in January, 2002. In April, 2002, I was notified that I was elligible for benefits as of Jan., & started receiving monthly benefits as well as a check for retroactive benefits (Jan-March). They counted my being disabled as starting in August, 2001. >When do you know if it's severe enough? If you can't work because of pain or nausea or because you're taking pain-killers, its severe enough. > Does anyone else have most of their pain located in their back? Most of the time my flare-ups start as either nausea or as back pain, just below where the bra strap lies. Hope some of this is helpful. Please feel free to ask any questions which may arise. jang Quote Link to comment Share on other sites More sharing options...
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