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272 total results
Comments (244)
@kuma My dr never prescribed pain medication for Raynaud’s but a vasodilator to increase blood flow....
https://connect.mayoclinic.org/comment/1413957/
never prescribed pain medication for Raynaud ... ’s but a vasodilator to increase blood ... supplement, beneficial for both my Raynaud ... ’s and SLE.
My aunt had a severe case of Raynaud’s
https://connect.mayoclinic.org/comment/1173704/
My aunt had a severe case of Raynaud ... aunt had a severe case of Raynaud’s
I am zero-negative RA, sero-negative Sjogren’s, Raynaud’s and Behcet’s. It’s quite an autoimmune cocktail to live...
https://connect.mayoclinic.org/comment/1572022/
zero-negative RA, sero-negative Sjogren’s, ... Raynaud’s and Behcet’s. ... It’s quite an autoimmune cocktail to
There articles including Raynaud’s. Association. Have found the genetic genes. Above are three links. The US...
https://connect.mayoclinic.org/comment/1454057/
There articles including Raynaud’s.
Yes, you are correct Sue. I have both and Raynaud’s too. I was diagnosed with Raynaud’s...
https://connect.mayoclinic.org/comment/1247765/
I have both and Raynaud’s too. ... I was diagnosed with Raynaud’s back
I just started LDN a month ago for an autoimmune skin disorder, and was very surprised...
https://connect.mayoclinic.org/comment/1374699/
when it significantly improved my Raynaud ... ’s!
Hi @kaps2065 and welcome to Mayo Clinic Connect. If you are comfortable sharing it will help...
https://connect.mayoclinic.org/comment/1470894/
you ask how to decrease pain with Raynaud ... I am familiar with Raynaud’s, though ... My coworker has a type of Raynaud’s ... photos and told me my fingers were Raynaud ... ’s is provided in this link:
- Raynaud
I have Polyneuropathy because a very rare autoimmune disease damaged my nerves. That happened 10 years...
https://connect.mayoclinic.org/comment/1575466/
I have Raynaud’s in my fingers and toes
@SusanEllen66, you mentioned other 'gifts' of cPAN including peripheral neuropathy and Raynaud’s. I’m with you: last...
https://connect.mayoclinic.org/comment/819008/
including peripheral neuropathy and Raynaud ... ’s. ... cold feet haven’t progressed into Raynaud ... in photos of folks experiencing a Raynaud ... ’s episode.
@ogl and others, there is another discussion that you also might want to read through. Raynaud's...
https://connect.mayoclinic.org/comment/954010/
Raynaud's Syndrome: Anyone want ... to talk about Raynaud’s? ... /connect.mayoclinic.org/discussion/raynauds-syndrome
It sounds like Tremors Essential & Raynaud’s Disease. I had to get a second opinion the...
https://connect.mayoclinic.org/comment/1272183/
sounds like Tremors Essential & Raynaud ... ’s Disease. ... come to the conclusion that I have Raynaud ... ’s Disease not Parkinson’s Disease
Yes, I’m living with Raynaud’s, and I had cold urticaria as a child/teen. I’m living in...
https://connect.mayoclinic.org/comment/1243193/
Yes, I’m living with Raynaud’s, and ... My Raynaud’s is genetic: my mother, ... weird I had cold urticaria and have Raynaud ... ’s now. ... It went away, but was replaced by Raynaud
=Please tell,them it’s impossible for,you to do,these infusions at home; they can ‘code’ it for hand...
https://connect.mayoclinic.org/comment/1566598/
=Please tell,them it’s impossible for ... can ‘code’ it for hand arthritis, raynaud ... ’s, , limited dexterity, or anything ... you might also,have—even if it’s minor
Raynaud’s is more pronounced in my feet but also in my hands on occasion. Swelling, burning,...
https://connect.mayoclinic.org/comment/842184/
Raynaud’s is more pronounced in my feet ... when blood work came back she said Raynaud ... ’s. ... Covid vaccine had something to do with Raynaud ... ’s peaking through.
For me it took a few months. At first, I was diagnosed with Raynaud’s Syndrome. My...
https://connect.mayoclinic.org/comment/213711/
At first, I was diagnosed with Raynaud ... ’s Syndrome.
I live in Vermont and use to suffer immensely from my Raynaud’s Syndrome. However, I discovered...
https://connect.mayoclinic.org/comment/917061/
and use to suffer immensely from my Raynaud ... ’s Syndrome. ... I discovered through research that Raynaud ... link to an article on beet root and Raynaud ... ’s.
@jayjaydoubleu. Welcome to Mayo Clinic Connect! There are several discussions on Raynaud’s syndrome. I tried to...
https://connect.mayoclinic.org/comment/1109610/
There are several discussions on Raynaud ... ’s syndrome. ... Here is one on Raynaud’s you can read ... /connect.mayoclinic.org/discussion/raynauds-syndrome ... Then type in ‘Raynaud’s’ into the box
Hi. I was recently diagnosed with Raynaud’s. I could have had it for decades and managed...
https://connect.mayoclinic.org/comment/1204672/
I was recently diagnosed with Raynaud ... ’s. ... apparently 45 is late for onset of Raynaud ... ’s primary or secondary)- I’ve had an
One more quick note, I forgot to put it in. I also have had Raynaud’s for...
https://connect.mayoclinic.org/comment/1025929/
I also have had Raynaud’s for years ... realize until I developed Sjogren’s
I have seen vascular and I have good blood flow in my legs and feet. I...
https://connect.mayoclinic.org/comment/878216/
It’s the Raynaud’s that is killing me
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