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  • Mrbshoney
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    Post count: 4

    Nancy – at last someone who has "been there", it seems a little rarer than other symptoms of the disease. I did start this with a little apparent swelling in my feet and a bad case of the orange-peel skin on my ankles and about halfway up my legs, all the way around, not just on the front. The legs finally eased off and now the rash is concentrated around my ankles (and up about 4 inches above them), but the protein deposition is severe in my feet. I have grown 2-1/2 shoe sizes, and my big toes are so swollen that my physician fears I might lose them. Prednisone doesn’t touch this – I use Ultravate, under plastic, every night for 5-7 days and then have to do a taper to stop. I’m good for a few days (still 2-1/2 sizes too large for my regular shoes), then the hard skin returns.

    I am also thankful that this is not concentrating on my eyes, and also that itching is not too much of a problem. I sure was hoping to hear that it might someday disappear completely…

    Mrbshoney
    Participant
    Post count: 4

    Ski’s description of my pretibial myxedema is correct – no lesions or cracking, but it does get very dry if not hydrated with lotion. I have been wearing strong compression hose to encourage circulation in my legs in an attempt to flush out the protein that is deposited under the skin. The swelling is not like regular edema (from excess fluid), but is firm and balloons up without the pressure. I appreciate all of your suggestions.

    Mrbshoney
    Participant
    Post count: 4

    Thank you for the suggestions. I live in an area without access to many specialists, but have seen a couple of dermatologists – they say "hmmmm, interesting. Sorry, I don’t know much about this…" I understand that they don’t have much occasion to see cases here. I have also been to the Mayo Clinic in Mesa and received much the same reaction. It seems we who are distinguished by having Graves Disease are unique…and interesting.

Viewing 3 posts - 1 through 3 (of 3 total)