Self help for Fibromyalgia
Posted , 11 users are following.
I have found some really useful information for anyone wanting to try to manage their symptoms by self help. If you try searching under - CFIDS Fibromyalgia self help - there are lots of useful articles, tips and success stories. Hope its of use to some of you out there. x
1 like, 18 replies
joy47826 denise56617
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nitropilot denise56617
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Thank you for the info. I went to the official site. It has a lot of research information, which is awesome.
The webinar series to help us manage our symptoms looks promising as long as it's not one big advertisement. In my experience, like with Functional Bioanalysis, there are practitioners but the site gives you a wealth of information for free - without trying to sell you anything or get you on some kind of drug.
denise56617 nitropilot
Posted
The supplements info is very interesting as it tells you what each supplement does.It mentions quite a few of the supplements that Joy takes (previous post) It also suggests only trying one supplement at a time so you can see if it has any positive benefits on you. It also suggests stopping each supplement for a short time after taking it for a year to see if you are still benefitting from it. I don't take many supplements at the moment but this seems very sound advice so I think I will investigate this further.
alig39 denise56617
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denise56617 alig39
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alig39 denise56617
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alexis10 denise56617
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anne90395 alexis10
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I don't know about the other meds, but my Doctor will only prescribe Amitriptylene, as he says other have horrible side effects. Also none really solve the problem from what I have read on this website. I find amitriptylene helps with sleep and a certain amount with pain. I am thinking this is the best it can get! Others seem no better of with truck loads of drugs!
Take care,Anne
denise56617 alexis10
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denise56617 anne90395
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nitropilot alexis10
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JulieBadger alexis10
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Good Luck
haytophill alexis10
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Until 6 months ago, I was on Methotrexate (RA) & Hydroxychloriquine (RA), Omeprazole (stomach), Folic Acid (stomach + counter Methotrexate), plus the usual pain management of Gabapentin + Paracetamol, Tramadol, 75mg Amiltriptylene (to help sleep ?).
My usual monthly blood test included a test for CRP (Creative Reactive Protien) which is normally 41 mol in a band from 10 - 50 mol. Suddenly, this jumped to 1825 mol, ringing alarm bells at my surgery, with me getting phone calls after 6.0pm that dat, saying not to continue Methotreaxate, which I usually took on a Saturday for just this reason.
I was then taken off Omeprazole onto Peptac Pepermint Solution (yuk), which caused more stomach problems, so after 5 months, I went back onto Omeprazole. Problem with this is you can't take Gabapentin until two hours after Omeprazole.
For pain relief, up to 3600mg of Gabapentin a day plus 8 X 500mg Paracetamol is what I am allowed, currently on 2400mg Gabapentin. Amitriptyline can help sleep (up to 100mg per night) plus I take 10mg each morning to start the pain support.
Most of my pain is knees and thighs, I had accupunture through the NHS Physio, and that was a great help, as it stopped the feeling of tearing off skin mainly down the left leg at night. 10% Ibrupheren spread on painful joints can help (prescription only) and use the free gloves at petrol stations to apply, or you rick touching your eyes or mouth with traces still on them.
Rhus Tox Cream from Weleda also helps if pain specifically within one joint. The tablets which I use for my arthritic spaniel don't have much effect for me, but maybe worth trying.
I also get waves of pain through the muscles and bones in my right arm, down to and including the carpel and ulner tunnels. I find slight compression uning sport support items does help manage and greatly reduce the pain, I have one arm tube which I wear all day plus hand supports which last about 6 weeks due to wear and washing.
There's a lot in the reply, which I hope also helps others where their GPs are reluctant to prescribe. Not everything suits everybody, it's a case of trial and error, but there is good support medication available, plus NHS Pain Clinics, push your GP to more actively managing you, this has been the best thing for me.
caitriona47134 alexis10
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I think the meds depend on the type of pain you get and your bodies reaction to the meds
hope4cure denise56617
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no pain meds help to many side effects or I am allergic to them. Bios r not on the market long enough for me. I have read every study since 2010 and I'm not ready to accept them yet as I have read too many who have explained their side effects and suffered set backs.
also read many success stories on bios yet they stop working after a time because the body builds up antibodies to the drug then they no longer help.