i have aps and this is my story... (hughes syndrome/antiphospholipid syndrome) | APS Awareness
It's been a good six months since I have last posted something.. I was not thinking of posting this but I felt the urge to share my story with others. Hopefully this video helps someone like me, who doesn't know what aps is, who needs guidance, comparison, or simply a support friend. Also the people in my close circle who are confused as to what's been going on with me. I decided to finally open up in honor of APS Awareness Month. There are many names to this autoimmune disorder, antiphospholipid syndrome being the correct medical term, APS as an abbreviation, and also hughes syndrome or "sticky blood". If you want to reach out to me or want to connect and be support buddies you can reach me on my instagram @emmrami STAY STRONG AND KEEP FIGHTING, WE ARE WARRIORS!! tags to help people with aps reach this video: antiphospholipid syndrome , antiphospholipid antibody syndrome , antiphospholipid syndrome pregnancy , antiphospholipid symptoms , antiphospholipid syndrome story , sticky blood syndrome , hughes syndrome For Business Inquiries: [email protected]
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