Brachioradial pruritus. (severe itching on forearms and neck, no rash).
Does anyone know of this. I think its rare but does exist. My neurologist does not know about this. I have compression between my c5 and c6 cervical disk and have had alot of sun damage to my skin.
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@scarletmia2
I write this for my wife who in addition to the BRP she has also lost most of her sight.
According to her she is in constant itch and pain, 24 hours a day. Nothing has really helped, the CAPSACIN HP and the Enbrel relieve it somewhat. but that is it. Since she has lost most of her vision she has to rely on other senses. Some medications that had been recommended over the years dulled her senses and made her feel like in a fog. Been to 4 different Dermatologists, an Allergist, a Neurologist, Acupuncturist, whats left. Years ago I heard about a study that was going on in Eujope, Maybe Denmark not sure. I contacted the Dr but since she was so far away she did not want to comment on anything. I understood.
@ilyne
Well I don't live far from Brigham and Women's Hospital in Boston which is to me the best hospital around and I'm seriously wondering if I should see a neurologist out there because I know it's the nerves being pressed by the deteriorating discs however the itches now spreading beyond my shoulders and my neck but the scalp is itchy my my whole back is itchy I do have bad arthritis in my back so maybe those discs are pressing on all kinds of nerves I'm itchy all the time at night and somewhat during the day the Atarax helps a little I take it mostly at night to help calm it down I'm just worried how bad is it going to get I know they can replace discs if they're really bad they can put cadaver discs in or whatever I really don't want surgery on my discs
I’ve had this for many years and it’s just getting worse. My sheets are bloody when I wake upbecause I scratch myself so much when I sleep. Steroid creams are mildly effective and Atarax is somewhat helpful. However, I also have restless legs and patients with the restless legs should not be taking antihistamines because it makes that condition worse so most nights I just don’t sleep and I want to peel my skin off. Years ago my insurance paid for doxepin cream but now my insurance refuses to pay for it and in the states it’s almost $1000 a tube. But that did work better than clobetasol Cream and oral doxipin. I’ve also had a lot of chiropractic work, including traction, which really hasn’t done much
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Go to to the Mayo Clinic! Beg them to see you. Send them your records. After itching for 18 months and treated with pills, creams, and injections, the dermatologist I saw at the MAYO had me itch-free within a month after titrating my meds. They are the best!