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Nail Discoloration Disconcerting
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Lyme Disease
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Savedbygrace12
Regular Member
Joined : Jun 2019
Posts : 332
Posted 8/21/2019 11:53 PM (GMT 0)
Hey all I hope you’re all well.
Lately my nails aren’t as pale but on the moons and a bit above it’s almost a purplish color.
I’ve been worried about
it due to the Raynauds symptoms and suspecting my circulation hasn’t been great and the vein issues.
Anyone else experiencing anything similar and what do you suggest?
Thanks for all!!
Savedbygrace12
Regular Member
Joined : Jun 2019
Posts : 332
Posted 8/22/2019 6:27 PM (GMT 0)
I know I have lots of nail posts but no doctor who even gives much about
the nail changes I’ve had. This is why I come here for your guys advice and because you all understand Lyme and Co. struggles.
Little Bear (LB)
Veteran Member
Joined : Oct 2015
Posts : 687
Posted 8/22/2019 7:14 PM (GMT 0)
Hi Savedbygrace12!-
I have Raynaud's. I have seen my finger tips turn blue. But my toes are a lot worse.
Wearing gloves, thicker socks (if your feet are affected) can help.
I gently massage my toes until the blood flow comes back. Sometimes exercise (if you are able to) can help with circulation. Or just wiggling your fingers and toes.
Some doctors might prescribe calcium channel blockers, vasodilator, or antidepressant fluoxetine (Prozac).
At one of my appointments with my LLMD, she said that she would prescribe Prozac to me. For personal reasons, I didn't want to try the Prozac.
There are triggers for some people. For example, stress and caffeine can make your symptoms flare.
Best Wishes!
Savedbygrace12
Regular Member
Joined : Jun 2019
Posts : 332
Posted 8/22/2019 7:29 PM (GMT 0)
Thanks so much for your reply. I’ve been thinking about
gloves to use at work. I’ve been really struggling working lately. Constant pain in my legs and my fingers just aren’t making things easy. Also when I tell doctors about
my fingers and nails they shrug it off.
It’s a struggle.
I really appreciate your reply!
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