I’ve been taking prednisolone for 11 days now 15mg. I have a very tingling scalp. It’s really irritating and I’m scared my hair will begin to fall out.
Has anyone else experienced this. I have no headaches or other side effects that I am aware of yet!
Thank you
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Pangolin43
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I also had this unusual tingling in my scalp in the first month or so but certainly no hair loss or pain and headache. I have only been diagnosed since last October and haven’t had any more tingling to date. Now down to 7mg pred.
I’ve had a tingling scalp and the feeling I’m wearing a very tight bathing cap since I started taking pred in February 2020. I’ve got used to it now, but it is irritating and contributes to the general malaise and feeling of weirdness that I have found more difficult to bear than the aches and pains of PMR. I haven’t had any hair loss, but my hair has got curlier and wilder - but that could be the result of lockdown and no haircuts!I do hope the tingling eases for you soon.
I have not experienced what you describe after almost 3 months on Prednisolone. Try phoning the PMR helpline. The advisors have a wealth of experience to share.
I can't remember if it affected my scalp but a couple of nights after starting pred (15 mg) I had the most curious sensation all over, the best way I can describe it is it was like little things crawling all over me, but definitely the sensation was under the skin. At the time I thought, well, if this is the worst pred side effect I get, I can handle it. It was gone by morning and has never returned. Later I wondered if it was the inflammation being reduced, as it was after that I felt pretty much all better, although I'd had some relief within hours.
In regards to prednisone and hair issues. I was on pred for five months. Two weeks later. Half my hair fell out. Yuk! I’m now wearing wigs. I’m told it will start to regrow in a few months. I’m sure this doesn’t happen to everyone but it’s annoying!
I had a f!are recently which involved tingling and really painful scalp a d head stabbing pains. Upped the pre d to what everyone said was mega, but symptoms subsided in 24hours. But I've lived with this for over 2years now and am beginning to learn how to deal with a flare.I would suggest you keep in close contact with your rheumatology nurses as I do now.
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