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Real members of MyPrurigoTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyPrurigoTeam Member asked a question 💭
Colorado Springs, CO
March 15, 2024
 · 
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A MyPrurigoTeam Member

I feel his pain. I don’t know if anyone who has collected disability for this nightmare since there are meds to help the itch.
However, since this is a condition that is lifelong, with his docs help, he may have a chance. Best of luck.

March 16, 2024
A MyPrurigoTeam Member

Was coming to ask this very same question… this disease is physically and mentally devastating for my husband- up all night scratching and finally gets some reprieve around sunrise and then sleeps a few or so hours. He can’t work and barely goes anywhere in public because he doesn’t want anyone to see him and start rumors about what they think he has… my heart breaks for him and anyone that has to deal with this disease. Much love to you all.

March 16, 2024
A MyPrurigoTeam Member

I've wondered the same thing and many times have thought it definitely should be a condition that is recognized!!

March 15, 2024
A MyPrurigoTeam Member

@A MyPrurigoTeam Member hang in there. Nothing has helped my husband so far including the Dupixent however they are fixing to put him in Renviox (I’m sure I’m spelling that wrong) so praying that will help. He is also fixing to see a kidney and liver specialist as his doctor feels the liver might be the culprit for him. Praying for relief for you and all other suffering this disease

October 27, 2024
A MyPrurigoTeam Member

I still haven't found a medication or cream or lotion or topical to help!! I'm on Dupixent and have been since August of 2023, I'm no better, in fact I think I'm worse! I ask myself every day, why in the hell am I still here? I can't live my life like this much longer, it is killing me.

August 10, 2024

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