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Re: Pain Management?From: Anon (anonymous@obgyn.net)Wed Oct 30 09:29:35 2002
Folks: I'm a long time lurker, recently diagnosed. I usually have no urge to get into a shooting match with Kristi. But I could not let this post go. Please do not take everything she says about Pain Management as gospel. I have suffered migraines and cervical disc issues for years. I know a great deal about chronic pain and current therapies. Please do not believe that Pain Management physicians simply feel that endometriosis is menstrual cramps; and subsequently they don't know how to treat that type of chronic pain. While that may have been true for the physician that Kristi interacted with, to apply it with a broad brushstroke to all Pain Management physicians is untrue and unfair to the Pain Management field Pain Management physicians have a huge arsenal of weapons at their disposal today including a range of medications (long and short acting narcotics, antidepressants, antiseizure medications, anti-inflammatory to name just a few classes), radiofrequency ablative techniques, facet injections, trigger point injections, epidural steriod injections, physical therapy, TENS, massage therapy, biofeedback, and when helpful (usually done by the partnering OB/GYN) lap scopes for lysis if ablation of lesions, adhesions, UAE, and chronic pain mapping. Some Pain Management physicians are so into chronic pelvic pain that they do conscious pain mapping. Meaning you are sedated just enough that they get a lap scope into you, then touch the various parts of your pelvis to see the exact part of your pelvis that hurts so much. S/he then figures out what nerve innervates that organ/tissue and whether or not it can be destroyed or ablated to permanently relieve the pain. For some women, for the first time in their life they can say "THERE, right THERE, THAT'S what hurts!" And then the doc can say "BAM!" there goes the nerve to that piece of tissue, and no more pain. Granted that's a bit dramatic but you get my point about conscious pain mapping. Pain management docs are the ones that do pain mapping. If you want to talk to some women that are receiving chronic pain management currently for endometriosis, go here: http://neuro-mancer.mgh.harvard.edu/cgi-bin/forumdisplay.cgi?action=topics&forum=Chronic+Pain+2&number=258&DaysPrune=1000&LastLogin Do a search on endo and read the posts. There's a wealth of info there. They can tell you their current struggles, their gains, their experiences. And they can give you a perspective that is missing from Kristi's post. Please don't let one person's bad impression of Pain Management trick you into thinking all Pain Management docs are clueless schmucks who don't have a inkling about endo or managing the chronic pain that is associated with it. Good Pain Management for endometriosis CAN be found. The issue is that good Pain Management for **anything** is a Godsend. Finding it is not always easy. You will probably wind up seeing more than one doc before you find one that you like. And you need to be open to all therapies - not just the ones that *you* pick and chose. And you need to be willing to work in collaboration with the doc - rather than dictating to the doc how the treatment will go. Those are mandates not to endo and chronic pain, but to chronic pain *in general*. Those are the types of things you will learn over on MGH. Just my two cents - well, probably $0.79. A Newly Diagnosed Anon Migraines ACDF and now endometriosis
At Tue, 29 Oct 2002, Kristy wrote:
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