Hi! I feel scratching(my legs and lower back) for three months. Is it related with APS(lupus anticoagulant)? Best wishes to all...
Is scratching related to APS? - Hughes Syndrome A...
Is scratching related to APS?
Hi i get the itching. .,it drives me nuts.You havent changed any of your meds have you?as some meds do cause it...tramadol affects me like that.....but i itch like mad when i am flairing .I mentioned it to my rheumatologist last year who said that some people can itch during a flair.7
i hope that helps......happy itching 😆
take care Vicky
Thanks for your advice APsnotFab. Best wishes for you...
Some things as simple as changing Bath soap -laundry detergent etc. or change of meds - i get this and i have to go on a steroid cream , very expensive and i can only stay on it 14 days , and Dc. get pissie if i use it with out telling him and then when i do - he says use the cream HA HA
I believe the APS can and does cause it and another big culprit is NERVES and they can effect anything in my book .
I am hyper { have been all my life } so far anyways .
I also have HUGE problem with feet -- I am going threw it as we speak -- very painful and seeing a new podiatrist- been on prescription band aids for the last week{ not working but i have another week to go}
is really interfering with my walking and swimming for my Fatty liver problem. so skin all over can be effected !!
C & J
Hi jetjetjet! Its obviously that nerves are related with skin. I am sorry for your problem with your feet. And about bath soap and laundry detergent i use only baby natural product.
Best wishes to you...
May I ask about the fatty liver please? Reason is I had a fatty unkown cycst on mine years ago lots of pain. Is this related to APS?
i started showing fatty liver after 2009 when all my clotting was discovered-- they have no cause - i am considered NASH-when i bring up the APS they are nervous about listing it as such--I am high stage 3
stage 4 starts at 17.5 and my last fibro scan @ 100 % accuracy was 16 .7
I can't take any of the meds for it so my walking and swimming is all i can do-unfortunately i am having such a problem with my feet it is making it tough . i have till July
i have asked about the possibilities of the fat showing on Fibro could actually be clotts but that would take a Doppler ultra sound of which my Dc. didn't want to do because she said that treatment would be the same as the 2 anti's i am taking now . i disagree. That Dc. left FEB. first and i start with a new one{I AM NOT EXCITED ABOUT STARTING WITH NEW DC>!!!} i just got her trained in the last 4 years. anything else i can talk with you about please PM me if you would
Thanks Becca ----------------------------------- C & J
SORRY
I have found that when I am on a higher dose of Warfarin I itch more.
I must admit before I was diagnosed I had terrible itching on legs and sometimes arms and also middle lower back. Once I was put on warfarin and my INR got higher it seemed to go away What are your INRs at the moment. As long as mine stays 4.0 and above im not too bad.
Hate to mention this but I had a very itchy back, before problems due to APS, since being on Warfarin, no longer a problem may not have been connected but always wondered
I had that and it was a blood clot in the artery leading to my kidney