This is where RSA people can write an official RSA blog. Or you can allow certain trusted members to write from you.
You may decide to turn this blog off and keep everything in the Community blog area.
This may keep the site looking more dynamic.
Another example: This is where RSA... - Scleroderma & Ray...
Another example
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Another Heated Glove post
Like all all of you winters aren't fun but decided to go, it seems Raynauds can progress. Thought
Participants required for Raynaud's study
hands of people with Raynaud's phenomenon/disease, using infrared imaging. Some of you may have...
RSA - Leeds meeting on 13th June 2011
Chester. It would be nice to say hello to some of you if you are attending.
Participants required for Raynaud's study
hands of people with Raynaud's phenomenon/disease, using infrared imaging. Some of you may have...
Raynaud's Awareness Month
awareness online, so if you have a social media page you can share this photo too.
Thank you for...
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Another newbie and worried my problems are so much less than others on here!
MANY CONGRATULATIONS TO ANNE AND THE RSA FOR REACHING THE COOL MILLION
Any experience of Methotrexate please?
How long do you stay off work with Scleroderma/Polymyositis?Moderation team
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