FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions. |
|
Thread Tools | Display Modes |
![]() |
#31 | ||
|
|||
New Member
|
Hi Everyone,
I just joined the forum and I have been reading the various posts by everyone. I think that my case might be very similar to that of Sandy Kay. I live in the greater Los Angeles area and have suffered from chronic pancreatitis since my gall bladder went bad and was removed in 2004, I suffer from Chronic Pancreatitis, Sphincter of Oddi and Crohn's disease. My digestive system is a train wreck. Surgeries, and Procedures, only give me relief for so long. I have relied on pain medication to manage my pain. Due to the aforementioned, I have been on a feeding tube since March 18, 2013 when they shut my pancreas and stomach down. The docs were hoping that within 6 months I would be able to eat again with no pain; however, that was not the case. I have lost 60 pounds (which I did not need to lose - I could have lost 10 to 15 and been fine) and I have no energy or any quality of life since being on the feeding tube. At this point, my doctor referred me to a colleague of his who is a pancreatic surgeon who is trying to think outside the box and he referred me to the pain management group. The pancreatic surgeon told me about a pain pump, so I did a lot of research about them and found many articles that discussed it's use for the treatment of pain associated with chronic pancreatitis. However, when I visited the pain management center, the physician brought up the use of a spinal cord stimulator in addition to the use of a pain pump. He seemed to be in favor of the SCS hence I started doing research about their use in the treatment of pain assoiciated with CP. I have not had much success finding many articles about this treatment of pain from CP. Then I ran across the NEUROTALK site and the posts of Sandy Kay. I would like to learn more from everyone and also speak or email with Sandy Kay about her experiences as they seem very similar to my own. I am scheduled for the first epidural relating to CP in the next few weeks to see if I will recieve any relief. Thanks for listening and I will be attentive to this site. Regards, Richard Quote:
|
||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
Laminectomy for SCS scheduled for May 15 | SCS & Pain Pumps | |||
Nervous - Scheduled for my SCS Trial | SCS & Pain Pumps | |||
Surgery Scheduled | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Surgery Scheduled - UGH | Bipolar Disorder |