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Originally Posted by malawigirl08
I joined but didnt find it very helpful - much prefer here, this feels like home and more people use and answer.
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I feel the same way. *edit*
From what I see, there is very little info on treatment there or where things are going in terms of research. From what I have seen, the research are little mini studies they are doing and nothing of great significance.
This forum is an excellent repository of information with very knowledgeable and proactive people.
When I search the net, most treatments are still geared towards pushing Pharma drugs which is fine if the pain can't be treated otherwise, but bad if it makes you worse.
All I remember was when they gave me the diagnosis, of SFN at the Cleveland Clinic, they said they didn't know much about it and they could either give me Lyrica or Cymbalta.
These drugs made my symptoms worse as I was triggering all the time.
Until I started using supplements, I didn't have much releif.
*edit*
Thanks.