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DiscussionRaynaud's Syndrome: Anyone want to talk about Raynaud’s?
Autoimmune Diseases | Last Active: Dec 25, 2023 | Replies (225)Comment receiving replies
Replies to "Good Morning, I have had raynauds for about 20 years. Only getting worse. Mornings are very..."
My fingers do the same changing of color (white, gray, ruby red). You are so right, stay away from very cold or hot water. I took gloves off in -15 degrees F and couldn't get back on. Also had taken boots off as water got into boots. Couldn't get them back on. Got to cabin and used Hot water. Pain was unbearable I've had Raynauds for 55 years.
1. NIH, etc. feel it's genetic.
2. Toes tingle mostly at night.
There is no known cure. The tiny veins in fingers and feet are just there. Keep stress levels down. I know how you feel.
Weic,
Thank you for your input. What heat pads specifically and where can I buy them? Did you go to a cardiologist for Procardia who treated you for Raynaud's? Or has a rheumatologist helped you with possible remedies? My daughter has been struggling with freezing and burning in her hands for years with no relief. Are there no gloves made specially for Raynaud’s outside? I just can’t believe there is so little information on such a debilitating condition. Thank you for any guidance to meds, gloves, shoes, and special fabrics in sweaters or jackets or jumpsuits, etc. that make this tolerable. NMC