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#31 | ||
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It really sounds the same. Ive never heard of BFS. This is interesting to me. I have always had hyperexitabliliy of my nervous system, but never this pain, spasms, twitching and autonomic dysfunction anything like this. |
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#32 | ||
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Ragtop,
I am familiar with the bfs forum. My first symptoms were twitching and vibrating and they lead to the bfs forum. It's actually how I heard of sfn. When I started to get more symptoms and in particular the burning I came across a few posters that ultimately received skin biopsies that confirmed sfn. Drs ( I think ) use it as a bail out. One neuro said I have bfs and refused to entertain the idea of sfn. As health girl pointed out bfs and sfn seem very similar. If they are so similar it seems ridiculous to me that neuros would put people in that category without biopsy to rule out sfn |
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#33 | ||
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I don't know what to make of this ( maybe it's even just coincidence). The areas that I rub my compounded cream on twitch, shake and vibrate less than normal. My cream has 10% Diclofenac and 2% amitriptyline. Diclofenac is an antiinfmammatory. Do u think my vibrating may be thousands of muscle spasms happening very quickly due to tight/tense or inflamed muscles? This symptom ( twitching and vibrating ) were my first ones and have been with me every second of the day for a year. Happen every second in all areaS at the same time ( hundreds all over every minute) effects do wear off after a few hours. I HSve been taking extra strength Advil but it doesn't seem to do the same thing. Tonight before bed I only put the cream on my feet ( both) left side of lower back and left side of neck. My entire left side of body is vibrating much less. Thus is odd bc both sides of my body do this equally. I don't know.. Anybody with more knowledge care to throw their two cents in?
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#34 | ||
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I just wanted to ask how your symptoms compare to a month ago? Are you writing a journal? It can take a lot to distill what is useful over time. An example? Well, I have about three years (with a few "oh the humanity pauses involved) of journal. Pain scale just doesn't have the reverb I hoped and I stopped that after a few months. Yesterdays three feels like todays one in the mirror.
I usually note odd changes or that it id day so and so of this muscle in my calf soasming bad enough my leg is turning in. That sort of stuff. I'm pulling for some relief for you. Jon
__________________
I urge you to please notice when you are happy, and exclaim or murmur or think at some point, "If this isn't nice, I don't know what is." - Kurt Vonnegut "It's an art to live with pain, mix the light into grey"- Eddie Vedder Just because I cannot see it, doesn't mean I can't believe it! - Jack Skellington |
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#35 | ||
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Magnate
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--that benign fasciculation syndrome and small fiber neuropathy are quite the same thing, as small-fiber neuropathy refers specifically to dysfunction of small, unmyelinated and thinly myelinated sensory nerves and fasciculation involves muscle, and even the smallest muscles are ennervated by more thickly myelinated nerve fibers.
There's nothing that says, though, that a similar originating process or etiology may be behind both in some cases. Moreover, it is common to have mixed types of neuropathy, in which both myelinated and unmyelinated fibers are involved. Often, a process that attacks the axon--the nerve fiber itself, instead of the myelin covering--will affect both small and larger fibers. (Small-fiber syndromes, by definition, are axonal; larger fiber syndromes can be axonal, myelin-based, or both.) Last edited by glenntaj; 05-15-2015 at 06:00 AM. |
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#36 | ||
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Many of the BFS'ers talk about "hot spots" - an area that has the highest concentration of fasciculations. But, for many people the hot spots move around and I would say that very few had the symptoms limited to one specific area. Again, like SFN - the symptoms can wax and wane, change location, etc.
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"Thanks for this!" says: | janieg (05-14-2015) |
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#37 | ||
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"Thanks for this!" says: | janieg (05-14-2015) |
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#38 | ||
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#39 | ||
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I have on and off but not right now. It makes me really depressed to write things out and sends me to a mental breakdown. Plus, none of my neuros care and don't let me tell them all my symptoms antway. They look annoyed when I pull it out and don't let me past the first few symptoms |
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#40 | |||
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I'm so weird. |
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