Good afternoon, I’m sharing a post that was posted on APS’ Facebook Messenger posts.

www.instagram.com/p/DK4_asVM9EI/

In lieu of June being APS awareness month, I’m trying to share the same daily updates that both aps sites on instagram share. Again, If the links I share here don’t work, either follow them on instagram or go directly to their web pages.

Good afternoon everyone, I know it’s been almost a month since I last posted but life has been pretty crazy. The biggest thing has been dealing with drs regarding my health-isn’t that always a full time job when you have chronic illness (illnesses?)

I deal with a few autoimmune conditions-sjogrens, APS, I’ll post something here regarding what it is-different forms of arthritis, and anemia along with chronic pain and dysautonomia. All of these cause me issues I unfortunately have no control over and make life miserable most days.

https://www.instagram.com/p/DKUieIguvEx/?igsh=YnQxNTA3eWp5YzRt

Hopefully this link works—June is APSawareness month and their page and apssupport uk are both sharing info each day this month to educate people on the issues that APS can cause or contribute to. Sadly, not enough patients nor drs, are educated enough about this once “rare” condition.

If this link above does not work-go to instagram and check out apsfa or their actual website apsfa.org or apssupport uk, or their website aps-support.org.uk. They classify APS as an autoimmune disorder, however if you’ve got issues with blood clotting, I’d suggest finding out what your family history is and getting tested.

Ok, I have caught you up for now on my past month, hoping everyone here is/has had a better month and has a great rest of your week.