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@bjbail70

My son has APS since 2007. He has been on warfarin since 2007 with exception of being on pradaxa short time. He has had at least 3 TIA’s, aortic heart valve replacement 2020 and awaiting another aortic heart valve TAVR hopefully within a few weeks. He’s 53 and he also has diabetes 2. He is not on any drug current or since diagnosis for APS except warfarin. As far as hydroxychloraquine, I never knew that drug was an option for APS until now after reading some of these comments. I am his mother and took hydroxychlorquine (placqunil) for many years for rheumatoid arthritis. Never had a problem or side effects with that drug. Last 8 yrs I’ve been taking rituxan for rheumatoid. Works great! I am so glad to have stumbled upon this site/blog. Learning a lot about APS. I think you’ll be just fine taking placqunil. I do hv a question, does anyone with APS experience painful hands/feet or “burning” pain on back of your tongue? Son experiencing those problems now and don’t know why or how to treat. Thanks and prays for all with APS!

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Replies to "My son has APS since 2007. He has been on warfarin since 2007 with exception of..."

@bjbail70, it sounds like neurological symptoms for your son. I, too, have pain, numbness, weakness, burning, pins and needles, etc. hands/feet and get a painful, burning rash on chin/upper lip. There is something called burning mouth syndrome that you may want to look up. The hands/feet could be small fiber neuropathy or endothelial/microvascular dysfunction. I am 54 and dealing with very similar things as your son.

Hello @bjbail70, I would like to add my welcome to Connect along with @dlydailyhope and others. @dlydailyhope mentioned burning mouth syndrome as something to look up. I thought I would share a search link for Connect that lists the discussions, comments and more on burning mouth syndrome - https://connect.mayoclinic.org/search/?search=burning+mouth+syndrome. You can also type in other conditions and terms for searching to connect with other members with similar symptoms.