[shello]

Hi there,

I've had CRPS in the leg/foot since 2010, I have CRPS Type 2 from nerve damage. I've just joined to hopefully learn and share with others about CRPS and hopefully gain a better understanding of this syndrome. Look forward to talking and sharing.

Shello

[alt1268]

shello,

Welcome to the group is nice to have you. Sorry to hear you have this horrible disease. You will find this is a great place with kind people who are willing to give a lot helpful information. Feel free to ask questions, rant or rave or just participate.

Originally Posted by shello

Hi there,

I've had CRPS in the leg/foot since 2010, I have CRPS Type 2 from nerve damage. I've just joined to hopefully learn and share with others about CRPS and hopefully gain a better understanding of this syndrome. Look forward to talking and sharing.

Shello

[catra121]

Welcome to Neurotalk! Sorry that you have CRPS...it is a nasty thing. I've had it since 2009, though I have type I. This is a great place to get support and advice and to just connect with others who have this condition. It has made such a huge difference in my life connecting with the people on here and finally feeling like I am not alone. As Alt said...feel free to ask questions or even just vent. This is a good place filled with very suportive and understanding people who can really relate to what you go through on a daily basis with this monster.

[birchlake]

Shello, welcome to the forum! Sorry to meet you under these circumstances. Yes, a great place to learn, support others, and vent!

I have had CRPS in the foot since 2008, a complication of a (routine?) surgery.

No wonder you have to sign so much paperwork before you go under the knife!! HA.

Sense of humor is critical in dealing with this thing. Keep your chin up!

[daniella]

Just saying welcome and sorry you face this too. This is a very warm and educated community and I hope you benefit from it too.

[scots ox]

Welcome tp the site. I joined recently and it's been a great help.Hope you make lots of friends and get the support you need. At least most of you guys are in a country that understands the disease. UK is a bit backward!

[ginnie]

I want to welcome you to Neuro Talk. You have found a very supportive site that deals with alot of differnent medical issues. You are right on the forum to most help you. You will find information, and may be a few new friends to talk to. I came here in a very shakey state of mind, and found compassion and good friends. I never left, even when the worst of my cervical problems were fixed. I hope you feel free to ask any questions you want, and explore all the forums. You are welcome to join into any conversation you want to. Again welcome, we are glad to have you. ginnie