Advice please??: Has anyone ever had mottled legs... - LUPUS UK

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Advice please??

Karen1983 profile image
10 Replies

Has anyone ever had mottled legs like this just wandering why they could be this bad they feel so tired, heavy and painful. I do have livedo rectilarius.

Many thanks

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Karen1983 profile image
Karen1983
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10 Replies
happytulip profile image
happytulip

My legs look just like that. I've been told its livedo reticularis. It can worsen with a change in the weather. Its worse in the cold with me.

in reply tohappytulip

Yes me too.

Sara_A profile image
Sara_A

Yes it looks like the livedo reticularis, I have this too. Maybe the pain and heavy feeling is from the sluggish blood flow ( I think that's what I've read somewhere?!)

Have u got aps?

misty14 profile image
misty14

Hi Karen

My legs,arms and hands have it too. It's livedo reticular is as others have said, can be more prominent in a flare!. Your certainly not alone Karen!. Do you take circulation treatment?. X

Catlady56 profile image
Catlady56

Yes I get this too

Lupiknits profile image
Lupiknits

Another one here.

Karen1983 profile image
Karen1983

Thank you all for your replies I was tested for aps antibodies but didn't show up. Do you think that can change? As tests was over a year ago. I will show consultant my pics on next review. I'm not currently taking an circulation medication. Really appreciate your help. Keep well everyone x

in reply toKaren1983

I was tested too and nothing showed up for Hughes but I think it can be a seronegative - certain this is what I was told oh the APS HU community. It lists Livedo reticularis on my diagnosis's - I think I asked about this once and the rheum just said it's common threesome with Sjögren's and hypothyroidism - thicker blood. I tried aspirin but it made my nose bleeds worse.

Sara_A profile image
Sara_A in reply toKaren1983

Yes as far as im aware the antibodies can change so it may be a good idea for them to recheck it esp if u are symptomatic

in reply toSara_A

Thanks. Yes I am certainly very symptomatic of Hughes so will definitely ask at my next consultation in December. All my autoantibodies were negative when tested 2 years ago so got the brush off - although I was on maintenance dose of Prednisolone when tested. Then, six months later off steroids etc - my ANA showed up clear positive and high IgG, inflammation etc so was offered lip biopsy and bingo!

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