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#11 | ||
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Member
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Thanks guys. I am taking my meds as imstructed, but they don't heal u. My arms and legs feel permanently asleep. Permanent pins and needles in entire legs arms most of my back and abdomen . I just don't understand how this is all happening without dr finding anything. I feel like maybe the discs in my back have moved and they r pinching the cord ( two herniated discs but apparently not doing damage.). Anybody have ideas, what r the docs missing?
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#12 | ||
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Member
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Quote:
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#13 | ||
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Member
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Yes, Ana apparently normal
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#14 | ||
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Junior Member
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[QUOTE=jurgen975;1138389]
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Long story, short, I have been suffering from (idiopathic) SFN (and a few other things) for over 13+ years. Firstly, I have always understood that SFN never gets better (no such thing as being healed). It only gets progressively worse . If you "get better" and all the pain is gone, it's something else and not truly SFN. And secondly, mediations like gabapentin (etc) don't "cure" SFN. They are given to help relieve some of the pain. Reguards |
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#15 | |||
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Wisest Elder Ever
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I do believe there is no 100% cure. But I do think some PNs do get better either with lifestyle changes, and/or some supplements.
One can stop progression if a reason is found, and eliminated, and some healing is possible. The compressive neuropathies can heal. I had hypothyroid compression in my wrists, and they did improve with time once that cause was discovered. Some Toxin/drug PNs may improve if the offending agent is removed. Some diabetic PNs improve with lifestyle changes. But often they do not go away completely. Idiopathic just means no cause yet found. It is not really a true diagnosis either, but a just a descriptive term. The genetic neuropathies remain progressive however, (until research reveals some way to improve them, say perhaps stem cell treatments or a drug, etc).
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
Last edited by mrsD; 04-26-2015 at 05:04 PM. |
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"Thanks for this!" says: |
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#16 | ||
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Newly Joined
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#17 | ||
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Member
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[QUOTE=LMPinkereton;1138462]
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There is not much literature about this except that it is possible that it in reversable but that only happend is some cause after a period of 3 years.I have this for 6 years now. But a dapsone neuropathy is mostly a motor neuropathy.The professors i visited could not agree if this was a dapsone induced neuropathy or not and they didnt even know if i had a small fiber neuropathy or not nothing showed on my EMG. Secondly the neuropathy i have is very local. When i new i had a neuropathy i searched the internet for a cure and i came across a group in the netherlands that used acapuncture/electro ecapuncture and supplements. So i had more that 100 electro acapuncture treatments but i think 20 where more then enough to kill the worst pain i had.This treatment is very effective for killing pain and i took acethyl L carnitine/alpha lipioc acid for years. This didnt help so much but i didnt. Over the years i stopped this supplement. Even after those 100 electro acapuncture treatments the pain in my feet became worse but slowly demised till zero. I still had tingling so i tried something new actually its a protocol for people with a CIAP. I took 2000 IE vitamine D in combination with PEA and PEA cream for 3 weeks and after that a so now and then a pill with vitamine D. Actually i should do this for a half a year i dont see the need for this. its in dutch so you have to translate this http://www.neuropathie.nu/overige/ci...eschermen.html |
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#18 | ||
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Grand Magnate
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Welcome Midniteangel.
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__________________
Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
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#19 | ||
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Member
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[QUOTE=LMPinkereton;1138462]
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That's what I have read too... It just gets worse . That's what scares me cus I have it so bad already what's going to happen? It's not just my feet or hands etc. it's every inch. Ive been having blind spots in my vision and blury vision for a while now. Saw the eye doc yesterday she said my optic nerve is thinning and referred me to a specialist. Sooo scared about not being able to see. I know glen says he's improved but he's pretty much the only one...ahh. Trying to hang on. |
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#20 | |||
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Member
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Some can improve if their cause is identified and treated or removed and if the nerves can regenerate which generally take a long time.
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