Antiphospholipid Syndrome : 30 Years On - Dr. Graham Hughes 

What an incredible, incredible man

Very interesting talk... can’t believe, this is THE Dr. Hughes. 👍

Its an absolute nuisance of a disease. I was diagnosed with APS at 18 along with a DVT and I am and always have been a healthy athletic guy. Found out Xarelto wasn't working/conflicts with Toxoplasmosis ?? and now I'm on warfarin. Already having some side effects such as fatigue and bleeding.

I was diagnosed with APS just today by my incredible rheumatologist. I am a 39 year old male with Psoriatic Arthritis, and had what was considered a cryptogenic ischemic CVA three months ago. Upon reviewing my labs from the time of my stroke, my Dr. noticed that I tested positive for the lupus anticoagulant antibody. After a second round of labs, and another positive result, he determined my DX. I was very upset, at first, by the thought of this disease; having had a stroke has been stressful enough without the new added fear of clotting at any time. However, with time to process this, I am so thankful to know now what likely caused my stroke, and how easy it is to treat and prevent future occurrences with the use of anticoagulants. I am shocked, however, that it has taken three months, and countless physicians reviewing my case, for someone to finally catch that I have this syndrome. I’ve read that 1/3 of stroke patients under 50 present with APS. One would think that would be an automatic suspect for the genesis of a stroke in a patient as young as myself. Greater awareness of this disease is necessary within the medical community, especially in the specialties that treat stroke patients, namely cardiology and neurology. Leave it to my Rheumatologist to have found it- I always tell him his job is to solve medical puzzles! Thanks for the informative video, and for your work to understand and treat this disease.

Amazing Dr Hughes! Read about your discovery of this! I had a TIA and 11 days later had a stroke of the thalamus, eighth nucleus apparently, in 2018. Dr Hughes, I have had high anti- nuclear antibody titers, first discovered in August 2020 after a known tick bite. Titers for antinuclear antibodies are 1:1280 and 1:5120 discrete nuclear dot Pattern on all tests, the last being performed by EXAGEN. I think they use an automated system so I got a higher titer because of that. I understand most laboratories will stop at 1:1280 on dilution, and that the higher titer on EXAGEN Avise test is a greater number because of its specificity and automation, I believe. All extensive Auto antibodies testings have been negative until getting the highly sensitive Exagen AVISE test which showed positive anti-phosphatidylserine/prothrombin IgM and IgG. My stroke was presumed to be from high blood pressure, moving from pre-diabetes to mild degree of diabetes, and elevated cholesterol. I understand that all of these conditions contributed to me having a stroke. Now that I have this diagnosis, with negative on related analytes, including low likelihood of SLE currently, would you please comment on the type of specialist I should consider for the presumed anti phospholipid condition. I also had an equivocal anti-RNA POL III IgGs I have a very large family and two children of my own. I am interested in knowing to help my family and myself. I believe there is also some component positive for me for factor V Leiden. Would you kindly recommend the type of specialist/specialists I should seek I am from the United States if you could recommend anyone in particular who has the best knowledge I would travel also. Thank you in advance for replying. I would greatly appreciate it!

I was diagnosed with APL, what does has to do with my swollen legs and pain in legs, any advice??

My neurologist diagnosed me with APS when I experienced a TIA at age 42. Coumadin caused bleeding, so I just continued with high doses of aspirin. 5 years after my TIA, I had a heart attack. Now, my rheumatologist has me on Xarelto that I can barely afford since there is no generic option. Are there any other effective treatments for APS?

What can I eat? Recipes please😱