This is a closed group. They also have a public Facebook page at: https://www.facebook.com/APSFA.
A support page run by the APS Foundation of America, Inc., a nonprofit organization. This science-based medical information group and an informational source and a friendly support group for people who have Antiphospholipid Syndrome or for anyone who's lives are touched by it. It is sometimes referred to as APS, APLS, or APLA and is formerly known as Hughes Syndrome or "Sticky Blood" in the UK. APS is associated with recurrent clotting events including premature stroke, repeated miscarriages, phlebitis, venous thrombosis and pulmonary thromboembolism. If this disease touches your life in some way, please feel free to join in our discussions!
, TX
Accessible Location: No
Type of Organization | Private Facebook group |
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Categories | Disability Specific, Emotional Support |
Services offered in Spanish? | No |
Newsletter? | No |
Child Care Available? | No |
Age Range | All Ages |
Disability Categories | Medical Condition |
Does this organization belong to all disabilities? | No |
This organization belongs to these diagnoses | Antiphospholipid Syndrome (aPL) |
Is this a statewide parent group? | yes |
Website | https://www.facebook.com/groups/APSFriendsandFamily/ |
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