I’m only 23 so I don’t know how advanced mine has gotten. they didn’t show me. they barely explained it to me
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I was 18 and had 6 in my lungs. they said the same to me. I am currently 23 and am struggling to find a doctor to help me. I cannot get therapeutic. I’m on 15mg of Coumadin and a lovenox daily. throughout the years, I have come to find I have more than lupus anticoagulant. I am in so much pain daily. I also have Raynaud’s phenomenon, i’m having TIA’s, spinal stenosis, APS, 40% blockage in my carotid artery or something ( I just was released from the hospital for that), my heart rate jumps to 150 resting, my skin feels like I am laying on sharp rocks all over sometimes, not often, but it is so painful, migraines.. the list goes on. I was accepted into the mayo clinic in Rochester MN but I never sent back my triage papers BC I was losing my medical insurance that week and was overwhelmed with finances. I am begging for help as well. I look to the lupus anticoagulant group on Facebook as a family in need. they have helped me so much. I talk with all my problems and have actually had gotten correct information and was able to tell my doctor what was wrong for once. it’s just a support group, not a medical advise group. just making that clear. and I would love to help BC I am at my bottom with this disease. no one can understand except those whom have it