Each member has different experiences of Raynaud’s and/or scleroderma and sharing them can be helpful in many ways – for research and information as well as for support.
The RSA has just launched a new online resource as a way of us bringing the RSA community together. This new, free site is aimed to help people who are either suffering personally, or supporting someone else who is. It can even help people working in the field who want more ways to learn about the disease or help with it. Whatever the reason, comments on this website will be invaluable.
For people to use this site and want to return to it, we need good, interesting content and that’s where we need your help: we need your blogs, your comments and your questions. You don’t need to have blogged before, you just need to write about things that you may be affected by or interested in. Visit: http://raynauds.healthunlocked.com/ and on the top right hand side you will see the word "join" so just click there to register.
Remember, even if you don’t become a blogger, you can comment on other people’s posts once you have registered. Don’t hold back – wouldn’t you like your words to make a difference?
If you have any queries about healthunlocked contact Helen at the RSA on: