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DiscussionWhat can I expect with Antiphospholipid Syndrome (APS)?
Autoimmune Diseases | Last Active: Aug 13 1:09pm | Replies (191)Comment receiving replies
Replies to "My son has APS since 2007. He has been on warfarin since 2007 with exception of..."
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.
@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.