heidiapsfa's Page
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Such a terribly important cause. Thank you for featuring the even with us! I'm with ya!
As a Migraineur and an autoimmune patient, I found APS on my own and asked for testing by my neurologist. He looked slightly shocked he hadn't thought of it a...
June is Antiphospholipid Antibody Syndrome (APS) Awareness Month! at United States
June 2, 2009 to June 30, 2009
The APS Foundation of America, Inc. has designated June as National APS Awareness Month. We're doing all that we can to get the word out to get this rare blood clotting disorder more commonly known.
APS is associated with recurrent clotting event...
Can't attend, but hope it's a great event!
Profile Information
- In the online health communities I participate in, I'm:
- a Broadcaster (Getting the word out)
- The online health resource I contribute to most frequently is:
- http://www.apsfa.org
- This site is:
- my non-profit
- Another place where I contribute is:
- http://www.apsforum.com
- Which is:
- a community I manage/moderate
- I’m also on:
- http://www.twitter.com/apsfa
- It's:
- my twitter
- More about me (my health interests and reasons for joining WEGO Health)
- Vice President of APS Foundation of America, Inc.
Comment Wall (2 comments)
- At 9:13am on June 2, 2009,
Vanessa_Rhinesmith said…
- Welcome to WEGO Health, Heidi!
What brings you to our growing community of Health Activists? We have many community groups to fit a wide array of interests. I would encourage you to check them out!
Please let me know if you have any questions about how to get started - or if you can't quite find what you're looking for.
Be well,
Vanessa
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- At 8:06am on June 2, 2009,
Ellen S said…
- Thank you for RSVPing to our Twitter Power Tools event. I'm sorry APS won't be able to attend, but I do know that we will be having another soon and will be sure to let you know the details thru my Twitter as well as thru WEGO Health. Let's get the word out about APS!!!
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