Got spots

mig
mig Member Posts: 7,154
edited 22. Aug 2013, 18:32 in Living with Arthritis archive
Hello everyone,as well as ra I have lupus which only shows up on skin not in bloods,its been nearly 8 years since i had an outbreak,10 months ago I started on humira injections along with hydroxy,I have a blotch on the back of right hand and small spots on forearms and chest ,not lots but enough to concern me,yesterday I should have humired but on advise I put it off and phoned rheumatology ,the result is not to do the injection and go to see consultant on Monday afternoon ,I hope I don't have to stop it as life's improved since I've been on it.Pocket duties will be appreciated . Mig
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Comments

  • Boomer13
    Boomer13 Member Posts: 1,931
    edited 30. Nov -1, 00:00
    Oh Mig, Lupus too? I am sorry, that's really too much.

    Pocket duties done.

    xAnna
  • villier
    villier Member Posts: 4,426
    edited 30. Nov -1, 00:00
    Awe mig, as if you haven't enough to contend with, Lupus as well. I remember when the doc said to me when he thought I had it and know what you must feel like. I am in hospital on Monday getting my infusion but will be thinking about you very much, hope you are not in too much pain......................Marie xx (((())))
    Smile a while and while you smile
    smile another smile and soon there
    will be miles and miles of smiles
    just because you smiled I wish your
    day is full of Smiles
  • barbara12
    barbara12 Member Posts: 21,281
    edited 30. Nov -1, 00:00
    Hi Mig
    Aww bless I will have everything crossed for you that this is not a lupus flare..and you can continue with your meds...I remember how you saying how well it was working for you..please let us know how you get on xx
    Love
    Barbara
  • stickywicket
    stickywicket Member Posts: 27,764
    edited 30. Nov -1, 00:00
    I hope you don't have to stop it too, mig, and wild horses wouldn't keep me away on Monday. ((()))
    If at first you don't succeed, then skydiving definitely isn't for you.
    Steven Wright
  • Susiesoo
    Susiesoo Member Posts: 358
    edited 30. Nov -1, 00:00
    I will be there, too, Mig. Will keep fingers crossed for you.

    Susie
  • DebbieT
    DebbieT Member Posts: 1,033
    edited 30. Nov -1, 00:00
    I've heard lupus can be really hard going, I'm really sorry :( I hope you'll get the all clear on monday ((((hugs)))) x
    Healing Hugs
    Debbie.x
  • dreamdaisy
    dreamdaisy Member Posts: 31,520
    edited 30. Nov -1, 00:00
    Oh beggur. Dammit, s*d it and 'sear' (anagram :wink: ). Oh Mig, this doesn't sound good, rest assured I will be in your pocket on Monday. DD
    Have you got the despatches? No, I always walk like this. Eddie Braben
  • Megrose489
    Megrose489 Member Posts: 782
    edited 30. Nov -1, 00:00
    I'll be there too, mig. Hope it goes well.

    Meg
  • suzygirl
    suzygirl Member Posts: 2,005
    edited 30. Nov -1, 00:00
    Mig is Humira the same as Enbrel? If so that can cause lupus to flare unfortunately. I have SLE, do you have Discoid or SCLE? I hope it isn't the humira causing problems, when you have finally found a drug that helps. These auto immune beasts are a pig, always something to deal with.

    I wish you well for Monday. What are you using for the rash?
  • mig
    mig Member Posts: 7,154
    edited 30. Nov -1, 00:00
    It's sle ,it's only ever shown up on skin bloods have always been negative ,I'm not using anything at the moment,I used to have dermovate . Mig
  • dreamdaisy
    dreamdaisy Member Posts: 31,520
    edited 30. Nov -1, 00:00
    Hi Suzy, enbrel and humira are what my dad would have called 'same dog, different bit of string' but I say different dogs on the same bit of string.

    Oh mig, I really hope that the humira will prove not to be the culprit. How are the spots at the mo? Spreading? Reducing? Still the same? DD
    Have you got the despatches? No, I always walk like this. Eddie Braben
  • mig
    mig Member Posts: 7,154
    edited 30. Nov -1, 00:00
    They're still the same and still itchy. Mig
  • Toots
    Toots Member Posts: 483
    edited 30. Nov -1, 00:00
    So sorry to hear you've been dished up another bad lot, Mig. Will be thinking of you on Monday x
    Toots x
  • kentishlady
    kentishlady Member Posts: 809
    edited 30. Nov -1, 00:00
    Hello Mig. I'll be in your pocket too if there's room? Hope all goes well for you. Beryl. (((())))
  • applerose
    applerose Member Posts: 3,621
    edited 30. Nov -1, 00:00
    I'll be there Mig. Hope all goes well on Monday.
    Christine
  • stickywicket
    stickywicket Member Posts: 27,764
    edited 30. Nov -1, 00:00
    I'm still thinking of you, mig. I hope it goes well today. ((()))
    If at first you don't succeed, then skydiving definitely isn't for you.
    Steven Wright
  • mig
    mig Member Posts: 7,154
    edited 30. Nov -1, 00:00
    Thanks Sticky,just getting ready,still a bit itchy and spots on hands and forearms,appointments not till 3.30 so goodness knows what time I will be home.
    Just a little whimsy does anyone else keep a set of underwear for appointments or is it me . Mig
  • dreamdaisy
    dreamdaisy Member Posts: 31,520
    edited 30. Nov -1, 00:00
    I apologise for not wishing you well earlier - I had a late start and then an outing. You will be done by now and I hope you have an answer. As regards the underwear, are we talking the little black lace numbers? Thought so. :wink: DD
    Have you got the despatches? No, I always walk like this. Eddie Braben
  • barbara12
    barbara12 Member Posts: 21,281
    edited 30. Nov -1, 00:00
    Hope its all gone well Mig...(((())))xx
    Love
    Barbara
  • stickywicket
    stickywicket Member Posts: 27,764
    edited 30. Nov -1, 00:00
    mig wrote:
    Just a little whimsy does anyone else keep a set of underwear for appointments or is it me . Mig
    dreamdaisy wrote:
    are we talking the little black lace numbers?

    Lycra?
    If at first you don't succeed, then skydiving definitely isn't for you.
    Steven Wright
  • Toots
    Toots Member Posts: 483
    edited 30. Nov -1, 00:00
    Thinking of you Mig, hope it goes well for you x
    Toots x
  • mig
    mig Member Posts: 7,154
    edited 30. Nov -1, 00:00
    So consultant said she has never seen a lupus rash that looked like what I have but has ordered the lupus blood test done,she said neither does it look like anything to do with the humira but have had usual bloods done .So it's now off to GP to see what they come up with,could possibly be a trip to skin clinic.So I shall have a nice warm shower pjs on and humira feet up cup of tea job done.
    No not Lycra nor flimsy black things ,I go for comfort these days. Mig
  • stickywicket
    stickywicket Member Posts: 27,764
    edited 30. Nov -1, 00:00
    I think that sounds like good news, mig. I do hope so. Enjoy the cuppa. You've earned it.
    If at first you don't succeed, then skydiving definitely isn't for you.
    Steven Wright
  • Boomer13
    Boomer13 Member Posts: 1,931
    edited 30. Nov -1, 00:00
    No, you're not the only one re the underwear....Keep a set just for that, not black, lace or lycra :shock: .

    Could the spots be due to lupus vasculitis? I don't have lupus but have had various autoimmune phenomena one of which was vasculitis which caused red spots (petechiae) all over the backs of my hands wrists.

    I've heard that lupus can do this too and it's different from the typical lupus rash.

    Anna
  • dreamdaisy
    dreamdaisy Member Posts: 31,520
    edited 30. Nov -1, 00:00
    Oh, spherical objects. :( I hoped you would be more the wiser but, as usual, this malarkey doesn't care to oblige. :( Dammit. My thinking is that a referral to dermatology is in order and I hope it comes through sooner rather than later. DD
    Have you got the despatches? No, I always walk like this. Eddie Braben