Antiphospholipid Syndrome (APS) Case Files (Gut, Tinnitus, and Migraine) - Prof Graham Hughes 

I don't think Covid had anything to do with mine, I was diagnosed with APS last year after having symptoms of what I thought was clotting for years, I was just too young and fit to meet the criteria to be tested but I had problems none the less. I suffered a lot but I'm still alive and thankful! I survived clotting in my lungs, blocked arteries in my legs plus some terrible frostbite on my one foot. I stopped smoking, drinking, eating too much. My ears are always ringing, I usually cant feel my legs and my endurance is terrible, I would do anything to have normal again. Please save me Warfarin!

I have been taking Vitamin E Baby Aspirin and support socks, my legs feel so much better. I work 1Ohrs on my feet 4 days a week.

APS had a myriad of manifestations, and clinicians should be aware of this chameleon disease.

I've recently developed small numbers of petechiae appearing on my face (1-4 per day, more if I am doing strenuous exercise). Because of this, my doctor sent me for lab work which indicates APS. It will be 3 months to 1 year before I can be seen by a Rheumatologist. I have no history of blood clots. I wonder if the petechiae is a result of APS? I'm also concerned about imminent stroke because my grandmother had a massive stroke that incapacitated her for more than 2 years before she passed away.

Wondering what specialist should I see. I was diagnosed years ago., After 4 miscarriages, 16wks,20wks and 25 wks preterm birth, died 6 months later. My father had tia's but he had a history of drug abuse and grandmother his mom almost died of a blood clott. My symptoms are my legs have always ached as earlier as my 20's at work, support hose help somewhat, no migraines , no tinnitus , went for doppler studies nothing found but nothing else. Standing in place to wash dishes and standing in place in general my legs ache.I am going to try baby aspirin and vitamin E. No sure what else?

Very interesting! I was diagnosed APS 12 years ago. I had thyroid removed due to cancer 2 years ago. My dad has dvt, Ménière’s disease, my brother has celiac disease and my mom and I both have migraines. Could this all be related?

I recently got diagnosed with APS and lost eyesight from my left eye due to the clot but I lost half of my eyesoght from my left eye not full, now i am taking pills like Xcept vita-6 and loprin I want to ask what else should I follow?

This is what happens when get a flu shot every year.