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167 total results
Comments (148)
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.
@ktrubia208, I add my welcome. I invite you to join others dealing with Raynaud's in this...
https://connect.mayoclinic.org/comment/1061718/
invite you to join others dealing with Raynaud ... #39;s in this discussion group:
- Raynaud ... Syndrome: Anyone want to talk about Raynaud ... ’s? ... /connect.mayoclinic.org/discussion/raynauds-syndrome
@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
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.
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 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
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
Welcome to Mayo Clinic Connect. You have come to the right spot for information. Folks are...
https://connect.mayoclinic.org/comment/1067677/
husband suffer with neuropathy and Raynaud ... ’s syndrome.
Hello Helen, I see a PA in rheumatology on Thursday. I have PBC and Raynaud’s, both...
https://connect.mayoclinic.org/comment/602845/
I have PBC and Raynaud’s, both associated ... with Sjogren’s.
Thank you, Colleen. That article does help and I’ll try not to worry until my doctor...
https://connect.mayoclinic.org/comment/751214/
I will also join the Raynaud’s discussion
Wow, that was quite a line up!!! I think that PAD and Raynaud’s would be my...
https://connect.mayoclinic.org/comment/790010/
I think that PAD and Raynaud’s would
MCTD shows as a “speckled pattern” on lab tests. I have a combination of lupus, scleroderma...
https://connect.mayoclinic.org/comment/737187/
I also have Raynaud’s, inflammatory
@curiosityisa10 hello, I have peripheral neuropathy also and Raynaud’s disease. I would say, the very last...
https://connect.mayoclinic.org/comment/901049/
have peripheral neuropathy also and Raynaud ... ’s disease. ... say, the very last thing anyone with Raynaud ... ’s disease or any circulation problems ... I know it’s frustrating.
@ray666 Hi Ray, Cutaneous Polyarteritis Nodosa is a very rare form of Vasculitis. It’s an autoimmune...
https://connect.mayoclinic.org/comment/882730/
It’s an autoimmune disease. ... So, I have PN, and Raynaud’s disease
When I was first diagnosed with MCTD the Raynaud’s was severe in my hands, feet and...
https://connect.mayoclinic.org/comment/715269/
was first diagnosed with MCTD the Raynaud ... ’s was severe in my hands, feet and
This sounds VERY similar to the symptoms I experience. I have been diagnosed with fibromyalgia, central...
https://connect.mayoclinic.org/comment/960106/
fibromyalgia, central sensitization syndrome, Raynaud ... ’s syndrome.
My comment on hormones may only be helpful for women. When I stopped taking estrogen patch...
https://connect.mayoclinic.org/comment/953753/
Hands still get cold from Raynaud’s.
Hi Gina, I understand what Raynaud’s feels like and have had episodes off and on starting...
https://connect.mayoclinic.org/comment/919067/
Hi Gina,
I understand what Raynaud’ ... s feels like and have had episodes off ... deaf ears with the usual “ you have Raynauds ... ” as though that’s it, followed with ... haven’t met a doctor suffering with Raynaud
@mctdfibrofairy sounds like you live near me! I have fibromyalgia, Raynaud’s and severe polyneuropathy. I don’t...
https://connect.mayoclinic.org/comment/927326/
I have fibromyalgia, Raynaud’s and severe
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