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Junior Member
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#2 | ||
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Senior Member
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Lisa,
I was just going to mention massage, relaxation and meditation and gentle yoga. I see you have most of that covered. One way to get massage is to get PT w massage as part of the plan. I don't find it as good- they can't give you a whole hour of massage but they can give you some and are trained. Can you tell us exactly how much of what you are on- especially the baclofen? ANN |
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"Thanks for this!" says: | LisaLisa37 (12-14-2012), SallyC (12-13-2012) |
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#3 | ||
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Junior Member
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"Thanks for this!" says: | ANNagain (12-14-2012) |
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#4 | ||
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Junior Member
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"Thanks for this!" says: | ANNagain (12-14-2012) |
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#5 | |||
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Member
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So sorry your going thru so much pain. Im suffering from alot of nerve pain and spasticity also. You seem to have a whole pharmacy going on there. Too many meds at once can interfere with each other. When my pain got worse, my neuro upped my meds but that made me worse. I was taking 80mg baclofen daily and 50mg amitriptyline daily. I was having worse problems. He decreased the baclofen and added tizanadine for the spasms. Much better. I currently dont take anything for the nerve pain, so Im muddling thru the pain as best I can. Easier said then done tho. Im not big into taking alot of pills, never have been. But I take them religiously to avoid being in too much pain.
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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"Thanks for this!" says: |
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#6 | |||
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Grand Magnate
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hi lisa,
i'm also sorry you're going thru so much. unfortunately meds are tough. so much of it is trial and error and up/down with doses. then, when you're on so many it's difficult. the main thing is that you have a good pcp (hopefully an internist) that listen to you, believes you and validates you. then you have a team approach (with you as the leader) that can work. do you have a neurologist? did you have an mri? do you have any positive tests for MS? i'm on a lot of meds also. i'm also on a pain med and my pain dr does random urine tests. that's typical of what drs do when giving pain meds. they know you're a legit pt and not abusing. i hope your dr can tease apart what will help you the most.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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"Thanks for this!" says: |
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#7 | ||
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Junior Member
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Thank you everyone for your thoughtful responses! I am so grateful to have a platform to come and talk about all of this with people that understand what I'm going through. It has helped me so much! Hope you are all well today and hugging your loved ones tight after all of the senseless violence going on this week
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#8 | ||
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Junior Member
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Sorry to hear what you're going through. I also have the same symptoms, have taken the same meds that you are taking, also with no luck. The only thing that's worked for me is Requip (or Ropinirole) for spasms. For nerve pain, sometimes I use over the counter Neuragen from the diabetic section at Walgreens. Hope this helps. Nora
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"Thanks for this!" says: | LisaLisa37 (12-15-2012), SallyC (12-16-2012) |
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#9 | ||
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New Member
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Hope you find relief! ![]() Melanie |
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"Thanks for this!" says: | SallyC (05-14-2013) |
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