Tthere is no Pancreas Lipomatosis reported by people with Complex Regional Pain Syndrome yet. We study people who have Pancreas Lipomatosis and Complex Regional Pain Syndrome from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
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Complex regional pain syndrome (long lasting pain condition most often affecting one of the limbs (arms, legs, hands, or feet)) can be treated by Lyrica, Gabapentin, Cymbalta, Neurontin, Amitriptyline hydrochloride (latest reports from 2,387 Complex regional pain syndrome patients)
Pancreas lipomatosis (latest reports from 64 Pancreas lipomatosis patients).
On Aug, 30, 2016
No report is found.
* Approximation only. Some reports may have incomplete information.
Hi my name is Lance. I was diagnosed with RSD in 2005. I had it in my shoulder post surgery. I have not had a flare up in years but recently I had surgery to have my gallbladder removed. Now they found a hemangioma on my liver and I have the most severe burning pain in my leg and hip. I have also been getting headaches so bad it feels like my head is on fire. I have seen my Dr several times and have been told that I have cancer but then the next visit they say I'm not sure u have cancer. Now me and my wife are going crazy as we were sent to another Dr and she advised that it might be my RSD spreading. I was shocked I didn't even know that RSD could spread. Since then I have been reading up on the spreading of RSD and my symptoms match. My eyes have been giving me problems the burn and I can't see very well. My eye problems seem to come and go but when it comes it comes on strong with headaches and ringing in my ears. I don't know how much more I can take. My dr's office treats me like I'm a drug seeker and none of the pain medication they are giving me is working. I'm currently on fentonyl patches and they don't work or stay on... anyone have any ideas on what works best?
im so nervous I wake up every day with less sight I have a 4 year old son I try to be strong around him I got a very supported husband I thank god for that sometimes I think there better without me but I would never hurt my self I just feel that way sometimes very depressed
I have had CRPS for 2 years. Just a few nights ago I started experiencing stomach pain. My Doctor didn't know what was causing it so gave me a stomach pill that didn't help so I didn't take it. I take a lot of meds, more than I listed. Just last week the stomach pain was soo bad I couldn't get ...
I am desperate for help. I have been sick for 14 years. It started from a IV and it caused Complex Regional Pain Syndrome. I have been dealing with organs swelling and having to be removed. I started having thyroid issues in 06 as well my face on the left side started to atrophy. I found out ...
Hi my name is Lance. I was diagnosed with RSD in 2005. I had it in my shoulder post surgery. I have not had a flare up in years but recently I had surgery to have my gallbladder removed. Now they found a hemangioma on my liver and I have the most severe burning pain in my leg and hip. I have ...
Got cprs type 2 after carpol tunnel operation a year ago 😢 its moved up my arm and shoulder. Took 6 months to diagnose.....we live in south Africa were in the world can I find a possible treatment to put me in a remission. I'm only 41.
I had crps 8 years ago after an ankle fracture,researched and found a dr who commenced me on dibenzyline,the problem resolved after6 months. I am am now 4 months post ankle fracture (again !) and symptoms have returned. My ankle/leg is pink, ankle joint is swollen ,movement is limited,pain ...
Hi, am a 50 year old wife, mom & gram...disabled hairstylist with RSD/CRPS. I have treated since 2009 and have just weaned (stepped down) from all meds except Lorazepam. I can't afford health insurance, nor the cost of doctor visits/meds. Since all have been done, 2 weeks now, I have the most ...
Hello, my name is shawna i have had RSD (CRPS) for about 20 years now since i had my baby 2 years ago my pain is a million times worse. I am currently taking gralise I don't notice any difference. I RSD effects my right arm and both legs. I feel like i am going crazy trying to find a health ...
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