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Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index
Pages: 1 2 3 4 5 Showing 1 - 20 of 109 for the best pain medicine. (0.207 seconds)

... Welcome Shelia, Ariel, and Anne. As other people have told you, you've come to the best place for info and to get something off your chest if you need to. ... (13 replies)
... Hi Sheila. Welcome to the forum. I take Topamax and a beta blocker daily. When the pain is really bad I take a Vicodin but not more than 2 or 3 a day. You are lucky to have found a doc who is knowledgeable about this horrible monster. ... (13 replies)

... my pain doc tried to increase it to 2400mg but it made me too drowsy. ... (13 replies)
... it's different than an IV infusion. You could also look into a pain pump. ... (13 replies)
... Welcome! I'm new to RSD so I can't help you too much. I used to take neurontin for chronic shoulder pain and I hated the side effects. I always felt out of it. For my RSD I'm taking Baclofen which is for neuropathic pain and a muscle relaxant. It's helping me. ... (13 replies)
... Welcome to the board! ... (26 replies)
... I want to thank each one of you for all the information that you have given me.The neurotin has helped my husband,and hopefully all of you will find something to help also. ... (13 replies)
... aid to think about this disease. Presently it's easier to be treated like a number, go to every kind of doctor, arrive at each therapy appointment and go through the motions. This does not include all the trouble with workers comp and their uncompassionate ways. ... (13 replies)
... Hi Ariel and Anne and welcome to the board. I'm glad you found us. I think it sounds like you have a good doc for RSD already. It seems that most of the docs who "specialize" in RSD are anesthesiologists who are also pain management docs. I'm sorry your husband has this, but I hope he is getting good treatment. ... (13 replies)
... My husband, Ariel was diagnosed just over two months ago. But, the RSD is appearing very aggressive, stage three already. He had shoulder surgery and started experiencing severe pain in the hospital. ... (13 replies)
... Thank you all so much for the huge welcome to the group. ... (13 replies)
... Hello Shelia...welcome to the Boards. I know you will find it helpful and supportive just as I did when I found this site in September of this year. ... (13 replies)
... Hi Shelia and welcome to the board. As Edna said, this is a great place. Everyone is really nice and supportive so feel free to join in whenever you want. I've had RSD for 17 years. ... (13 replies)
... Hi fillycat and welcome to the boards. ... (6 replies)
... Was the best pain medicine by far. But Medicare doesnt cover it so I stay on MS Contin ER and IR. ... (6 replies)
... penrenmun...first i wanna say happy holidays. Secondly i completely understand you. After my car accident and losing a decent sized chunk of the soft tissue of my left leg, i developed rsd. ... (5 replies)
... ation 20020099425 for "Interferential current treatment apparatus". I'd include links but it seems this board does not permit linking externally if I understand the rules. An issued patent however is not proof of efficacy or safety. ... (22 replies)
... When I google CPS or chronic pain syndrome it does not say its related in any way to CRPS or chronic regional pain syndrome it describes it as a separate entity ( pain feeding on pain) (33 replies)
... I take Methadone for pain control, if there is such a thing with RSD. But I am taking 20mg two or three times a day as well as I wear the Fentanyl Patch 100's. I have used other pain medicines but they have made me very sick. I have no problems whatsoever with the Methadone. ... (18 replies)

Associated Tags: cps, flareups. fear, pain, rsd

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