Hi all,

I just joined this group to find support for my new diagnosis of CRPS in my right ankle. While I know being new one is supposed to open up and write or talk about one's story, I don't quite feel ready to do that yet...still trying to discover what CRPS will mean to my life.

Also trying to get the Drs to come up with a treatment plan that won't take weeks and months to activate...seems like the medical end of this is moving so slow. I'm sure it's just my perspective, since the pain & burning are so fierce sometimes...makes the Drs seem lazy!

Best to all...thanks for letting me vent in a tiny way.

Terri

Welcome TerriLHF.

Someone will be along to help.

Hello Terri,

Welcome to the NeuroTalk Support Groups.

We have a Reflex Sympathetic Dystrophy (RSD and CRPS) Forum

There's no pressure here about opening up and telling your whole story so
please don't worry about that. You will find support and information and right
now that's probably what you're looking for, so please don't worry.

you take care there

Terri,

It is great to have you come and be with us. You will find a great number of dear friends to listen when you are in need of ears. Please let us know how we can help you out. You will find out we are supportive and relaxing place.

Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene