anyone who has anti-phospholipids has... - Hughes Syndrome A...
anyone who has anti-phospholipids has problem in forefront feet orthopedic said it might cause arthritis that attacks the joints of the feet
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Sort of, I get sore feet, mostly right sided and in the arch, more recently, I feel as thoug a muscle has knotted just at my big toe, I massage the area, and the day after I have a lovely bruise, sometimes just a tiny one, but right now it's thumb sized. Sarahx
I have tendon damage that cause clawed toes in all my toes and my achilles Tendons are very tight due to shrinkage plus Neuropathy in both feet x
I have oddly over recent weeks had a burning sensation on top of my right foot. It is quite regular but nothing can be seen and I cannot think of anything that I have done to hurt it.
I get heel pain, stops me walking sometimes
I have pain in hands and feet. Having hand surgery soon.
Very educative the question posed and the comments posted. I'd been diagnosed with APS and have suffered pain in the forefeet for the past two years; according to my Immunologist the pain is not related to the Syndrome.What is helping to ease the pain is walking and practicing specific yoga poses. I live in Venezuela where perhaps medical care is not at England's level. Please do let me know your evolution.
I live in Lebanon and we have very good doctors I did several MRI for the feet and bone scan and doppler and the last was an Xray for the soles of the feet. I saw an Orthopedic who has come back to lebanon 2 years ago from Mayo clinic and he thinks that APS and Sjogrens as I have both may cause some kind of Arthritis as the joints of the toes are inflamed and can't walk more than 10 minutes he advised me to put medical insoles they are soft and it helped me. I'm seeing another Orthopedic next week and if he tells me I need an operation then I'll go to London UK as my Rheumatologist is in the Lupus center that was created by Dr Hughes and I was lucky enough to see him eight years ago before he retired and he diagnosed me as having APS. Another thing Dr Hughes told which is nice to know is, during a big medical convention attended by 400 Rheumatologists they decided it should be called after him Hughes Syndrome. I'll keep all who answered my questions posted after I see the doctors in London.
Do please keep us posted on your evolution. It seems to me that I'll have to consult Dr. Hughes sooner or late.
How do I know if Dr. Hughes ever comes to Venezuela? Do you know? If I ever go on consultation to London. what doctor will you recommend to me? My APS is a primary one.
Oh thanks a lot! Keep posting for all of us and take care