Fibromyalgia and the Pain Barrier

By: Emma Fabian (View Profile)

“In the end, I had to accept this is my pain,” Ali tells me. “And I was the only one who could deal with it. I decided to strengthen my back with Pilates and swimming. Massage, especially with heat, helps too.”

Jemma hit upon a more radical treatment. “I searched the Web and found a theory that a build-up of phosphate in the body can cause acute pain,” she tells me. “So I went to an osteopath who detected loads of lumps he said were phosphate. Then I started taking a medicine called guaifenesin (it’s a constituent of some cough medicines), which is supposed to help excrete it. I’m sure it’s working. My osteopath says there’s less lumps. I’m up and about and in far less pain now.”

For all the fuzziness that surrounds FM, the pain associated with it is all too sharp for the thousands of women if affects.

Perhaps by sharing experiences and becoming a loud voice that forces doctors to listen, then—just maybe—this pain can be collectively relieved.

 

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posted: 05.30.2008
FaithTrustHope
Dear Ones, I too had FM, probably since my teens. I did not identify it until I'd been dealing with CFIDS for a couple years. It was diagnosed by a rhemutologist (sp?). Because my muscles contracted sporadically, I decided to try ten sessions of Structural Integration (Rolfing). Within a couple sessions, I noticed much decreased pain in my body. This continues today unless I do a repetitive motion for some time (causes flare- ups) or drive for a couple hours. I pray that all with FM find what works for them. (My Structural Integration therapist says no other FM patients received the same benefits.)
posted: 02.29.2008
Rebecca
Very true. My mum suffered from FM and got no help from docs for years. They thought she was 'a lonely old lady' but we who knew her knew she was not a complainer and in the end they agreed but she had to work out for herself what helped. Moderate excercise and chamomile tea were two things she liked.
posted: 04.25.2007
Amy Shouse
Thank you for this article. It brought tears to my eyes. Not because there were diagnostic solutions offered (with FM, the "first noble truth" one must embrace is that there are no solutions from the outside) but because it felt GOOD to read about validating stories. So many aspects of FM are, like you said, invisible. The excruciating pain (on good days --- it's just "I sudeenly feel fluish and I don't know why") I live with is inexplicable and after a while I feel the need to simply not share what's going on with me. I recently turned quickly to look at my niece so I could watch something fantastic she was showing me. This ruined my neck and eventually my back for four days. How do I explain that to people who don't understand the illusive nature of FM? I'm committed to understanding this disease and to not give up on caring for myself. Your article was a reminder that I'm not alone and that is such a sweet breeze of relief and hope.
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