Does anyone else have MCTD with systemic sceladerma? Anyone else?

Posted by sonnyforee10 @sonnyforee10, Oct 8 6:23pm

Anyone else with MCTD overlap of systemic sceladerma? I know it’s serious and have lots of questions about it I ask my Dr and she’s very evasive answering. She says it’s ok you’re numbers aren’t that bad I need better answers anybody else

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grandmal65 | @grandmal65 | Oct 16 4:23pm

I am actually going through a Reynauds flare right now. Super cold hands and feet. I wear socks 24 hours and gloves maybe 12 hours a day. Painful at times.
I'm trying to reach my Neurosurgeon but apparently he's out sick. That doesn't sound good. Thank you for getting back to me so fast.

Hoping you're doing ok. Yes, feel free to message me. I love visiting.

Hugs!

sonnyforee10 | @sonnyforee10 | Oct 19 2:52pm

In reply to @grandmal65 "I am actually going through a Reynauds flare right now. Super cold hands and feet. I..." + (show)

@grandmal65

sonnyforee10 | @sonnyforee10 | Oct 19 2:55pm

Hi what type of meds do they have you on for Raymond’s. I’ve read where a Botox injection would help a lot? Anyone else hear that? They gave me generic viagra for min 3 pills a day only 10 mg

sonnyforee10 | @sonnyforee10 | Oct 19 2:56pm

In reply to @sonnyforee10 "@grandmal65" + (show)

@sonnyforee10 Hi what have they given you for Raymond’s? Hope you’re having a good day!!!

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