Raynaud's Syndrome: Anyone want to talk about Raynaud’s?
Anyone want to talk about Raynaud's Syndrome? My daughter has a severe case of it. I would like to start a support group here on Connect to find others, share our stories, treatments and managing daily life.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
bruizersmom, do you know if your Raynaud's is primary or secondary?
I don't even know the term. I was diagnosed after a teensie bit of frostbite...does that mean anything??
My granddaughter suffers terribly from Raynauds. However a couple of weeks ago she had a reverse symptom. Her fingertips became red and swollen and hot to the touch. She was treated with steroids and antibiotics. Is this the same thing or what could it have been?
I've had it for 30 years, it's worse in the winter with the cold weather as well as picking up ice cubes. I take beet root powder daily to increase my circulations, and I use a ball that I squeeze to keep the circulation moving. It's really helped me.
Hi mireckij
I've had Reynaud's for 60's years. My fingers turn Red, Blue,Green. I used to hunt and fish a lot in the Northern States including Canada (born in Quebec). When fingers get Blue or Green I can do very little. Never use hot water to warm fingers. Thank's for tip on heated gloves from Amazon.
Kevin