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Brachioradial pruritus. (severe itching on forearms and neck, no rash).
Skin Health | Last Active: Jul 11 6:06am | Replies (685)Comment receiving replies
Been to two dermatologist who think I have brachioradial pruritus because I told them I think I have it after doing research.,they cannot help me they did not know anything about it. I have an appointment scheduled for February with a neurologist. I have been waiting for this appointment since October. I call every day to try to get in sooner. I am going mad. I get maybe 3 hours of total sleep. I actually took a knife to my arm and made a cut. I was thinking cutting it off , but woke up and realized not a good idea. I am going crazy. I thought about going to ER , but they will not be able to help me. I know I will need MRI etc. My question is will it ever subside? Can they burn the nerves? I tried gabapentin, but made me too foggy so I stopped. I called the dr's crying . I believe the really do not care. I need help
Replies to "Been to two dermatologist who think I have brachioradial pruritus because I told them I think..."
Bonnie- google the Miami Itch Clinic - Dr. Gil Yosipovitch, MD. He is the itch guru- many docs are NOT up on this itching issue. I find myself having to educate them! Also google Dr. Yosipovitch on you tube this past November, 2018. He explains a lot!!! Currently however the best most MD’s do is prescribed a CNS med- you can try other ones besides gabapentin, like amitriptyline or others; and some dermatologists like Dr. Yosipovitch are well versed in compounded creams, that do work well for many.
The PIT injections may take time, so you need something to hold you over. Also you would need to find a skilled functional medicine doc trained in this treatment. I prefer a functional medicine MD but they are hard to find unless you are close to a larger city. There may be some very good DO’s or ND’s that have a successful track record with this.
Itching your arms is pointless. There isn’t anything external.....if it is a neurogenic itch, it is deep, and the scratching only makes it worse. Ice is also a good temporary measure. You can get those pea ice packs at cvs.
Also don’t be disappointed if you find nothing from the neurologist or neurosurgeon. That happened to me. I had spinal xrays and a spinal MRI. It showed some foraminal narrowing but I gave no joint pain and they only treat with medicines and surgery if you have joint pain. Finding nerve entrapment requires a neural MRI and that is a new technology. But my functional MD knows how to look for that by just applying pressure to specific nerves. He if the one giving me the PIT injections. I have only had one treatment and still need the compounded cream. I think I am getting gradual results but it is too early to tell for me.
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Please get back on the Gabapentin-you will adjust. I take one with breakfast, lunch, & before I get ready for bed. I shower fully every other day, but wash the needed areas the other days. Not getting the burning area in too much water seems to help( try to use cooler water). I’m seeing a Neurosurgeon on Thursday, so I will let you know what he says. Someone mentioned that Lexapro helps-maybe your regular doctor can help. I can’t imagine having to wait so long for help. Are there any large cities nearby where you could see a Neurosurgeon sooner? I have a hot/cold wrap that I keep in the freezer. This gives relief. Please keep in touch. I’m praying for you!