just a quickie as GP didn’t have any idea 😳. I know we’re not Drs and can’t diagnose but has anyone had this rash before ?
both legs lasted 2 weeks . Didn’t itch
Thank you sooo much for looking . Hugs , ☕️ 🍫 for all xxxx
just a quickie as GP didn’t have any idea 😳. I know we’re not Drs and can’t diagnose but has anyone had this rash before ?
both legs lasted 2 weeks . Didn’t itch
Thank you sooo much for looking . Hugs , ☕️ 🍫 for all xxxx
HiNot sure
Could be lupus related
Thank you ☺️ pharmacist said systemic 👍
Your welcome yes definitely I had it before not as much rheumatologist saw purpura if search it images .
Rheumatologist or dermatologist needed can you email in photos to rheumatologist nurse helpline .I have that option because my cancer
I get it on my feet
There few types of purpura Can be any those
You have alot I'd send in pics glad help mine was much milder.
All best update us ☺️
Ok that's best rheumatologist will put it on file glad didn't last long
I had loads of small pimples on both my forearms, just skin coloured, my rheumatologist felt them and didn’t seem bothered. Investrust lupus, systemic scelerderma and myositis. They are slowly slowly fading away.
I’ve had these a few times over the years but I’m only recently diagnosed lupus sle.
Take care
Wendy xx
Hi Tiggywoos,
I have had something similar during a bad flare. No itchy stung when showering. GP didn’t know what it was and my then Rheumatologist said : I am not a Dermatologist”. So I was never any wiser sorry xxx
Blimey Charlie. That looks so sore 😢xx
The pain was from inside the legs really. My Rheumatologist was so disinterested. He actually shrugged 😡 xxx
Eeek yes you’re right the calves were painful .. think we get so used to pain we sort of file it 🤦♀️xx
It is painful. I struggle to walk anyway with two knackered knees so it was quite debilitating for me. Xxx
Nice to know you were taken seriously 🤦♀️😭xxx
I don’t think I ever have been to be honest 🫤 xxx
we all love you and take you seriously 😘❤️xxx (ps I know what you mean 😳)
Oh bless you. That is so kind of you. I meant the Rheumatologists. I had a Rheumatology Nurse tell me last month that it was patients like me that made life difficult for clinicians like her. I had just told her that I had booked my DMards bloods but ended up in A&E until 3 am with a blocked bowel. You really do have to wonder about these people and why they do their job xxx
I sort of have no words 😶.. I think I nice juicy pension and plenty of sick pay might have something to do with it for some not all but some 🤦♀️xx
My GP wanted to make a complaint for me but I will do it myself if she keeps it up. The last one said that it was no wonder I was in pain given my weight. She asked if I had heard is salads and remarked someone my size should never eat carbs. I was honestly speechless. I am a vegetarian and have salad 4-5 tines a week. What gives them the right to judge? They should walk a mile in our shoes xxx
I have SLE and yes I get this all the time on both legs. Can go quiet for a few days and then back come more. My legs are permanently marked now. My rheumatology has always said it is Purpura. Had the ANCA test, negative, so it's no Vasculitis. Hope this helps.
Gosh that’s so interesting thank you ! As I do have permanent marks on one leg and the others come and go like yours . Had blood test yesterday for Betchets .. xx
Cecily parsley knows about that I think and I see she’s in this thread already and hope she may help
I've never heard of blechets, please post the results. I was diagnosed with SLE in 1979, so I have had many years of Lupus flares and everything that goes along with Lupus life. The rash was actually my very first symptom, at that time it took 2 years to diagnose. Be happy to answer any other questions you have, if I can help. X
That’s so kind thank you …. I’m like many others on here bounced around with diagnoses … Betchets pretty rare I think and apparently you can test positive and not have it . Blimey we’re a complicated autoimmune bunch on here ! You’ve had lupus a long time 😞😘xxx
Looks like some kind DEPIGMENTATION/over pigmentation ?process going on, very speckled?
Query vitiligo? which is an autoimmune condition with T lymphocytes attacking melanocytes, pigment cells differentially.🧐
Darker skin sufferers get whitish patches all over?!
BTW I would definitely NOT expect any GP to be a competent dermatologist these days or ever. They simply do not have the training. No apologies.☝️🤣
I’ve got SCLE properly diagnosed now vitiligo is knocking on the door! Sad.
Thank you suvi and you’ve raised interesting point . I do have vitiligo on my left arm which I thought was prob just side effect of hydroxy as been on it years . The legs rash was different to my arms . Be interesting ti see what rheumy says if anything .
I’m sorry about your vitiligo is it all over ? . My GP shakes when he looks in my ears 🙄 so my expectations are low when it comes to him looking at rashes that’s why I went to pharmacist 😂🤦♀️xx