posted
i am experiencing toes turning purple and going numb... happening more often. whats going on?
Posts: 11 | From Ft. Wayne,IN | Registered: Dec 2009
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Ohhh. What does your doctor say about this?
Have they assessed you for Raynauld's?
Do you have a LLMD? Some lyme patients to experience this and it often gets better with treatment. -
Posts: 48021 | From Tree House | Registered: Jul 2007
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sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270
posted
My mother has "raynaulds" and that is what her fingers do exactly. Can happen to your fingers or your toes.
Posts: 4035 | From Mississippi | Registered: Jul 2008
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posted
My toes have never turned purple but numbness... had it all the time as did my close friend with Lyme. Definitely follow up on the purple part though, suggestions above sound right.
Posts: 24 | From Connecticut | Registered: Jan 2010
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-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96239 | From Texas | Registered: Feb 2001
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Pinelady
Frequent Contributor (5K+ posts)
Member # 18524
posted
Could be Lyme. With Raynaud's. My daughter just
showed me her hot red burning toes. I said hey I
remember those. I had them over a year ago. Now go
take your medicine. I saw a show the other day on a
truck driver who suffered over a year and almost
lost his feet. He had a blood infection.
-------------------- Suspected Lyme 07 Test neg One band migrating in IgG region unable to identify.Igenex Jan.09IFA titer 1:40 IND IgM neg pos 31 +++ 34 IND 39 IND 41 IND 83-93 + DX:Neuroborreliosis Posts: 5850 | From Kentucky | Registered: Dec 2008
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posted
I have SEVERE Raynaud's that seems to be getting worse. My fingers and toes are affected. My fingers get so white, then they can turn any color from red to purple to even BLACK! The doctors have seen it in person! What IS the treatment for this?
My doctors all know I suffer from this, however nobody seems to be treating it. I guess they think it will improve on it's own? I'm on Toprol for heart issues and I've been told that the only real "semi-treatment" is some other type of vascular diaoltor med or something similar to that.
Apparently, none of my doctors want to put me on a med like that for multiple reasons ------- other health issues, etc. I don't know, but SOMETHING MUST BE DONE!
I have a call into my neurologist and cardiologist right now. What med do some of YOU take to help with your Raynaud's?
Thanks so much for any suggestions!
terri3boys
Posts: 268 | From Texas | Registered: Aug 2007
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-------------------- I'm sorry but I am no longer accepting any private messages due to my own battle with lyme. Posts: 3897 | From New Hampshire | Registered: Jun 2008
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