I’ve been on Prednisolone for over 6 years having once managed to come off last May. Unfortunately I had to go back on due to symptoms returning. For most of the time, my nails have been in better condition than ever in my life, but this last year I’ve developed very odd white marks on several nails. (See pic) Has anyone else had this problem & if so, how do you deal with it? I’ve consulted Doctor Google & come up with a possibility…onycholysis🤔 Any help would be gratefully received thank you!
Nail problem: I’ve been on Prednisolone for over... - PMRGCAuk
Nail problem
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Are they only at the tips? Or did they start further down the nail and grow out to there?
My nails do that occasionally and then they look OK again over time. Your nails look so like mine in shape, colour etc, they could be twins. It happened to my nails before I got PMR. They seem OK at the moment.
Thanks. I’m hoping they get no worse!
I have often wondered why it happens. Perhaps I will take more notice now you have mentioned it!!
I have looked it up.
‘Onycholysis is a common nail disorder in which the nail plate has separated from the nailbed typically resulting in a well-defined area of white opaque nail.’
There is also leukonychia - white spots that grow up through the nail, due to nailbed damage. Can even be caused by the nail technician - though that will never be the case for me!!!
I get those occasionally too. In fact I have a small one now. Onycholysis seems to happen at the top of the nail while leukonychia seems to be white dots further down. They say that you can tell a lot about the health of an individual through their nails. A window to our overall health!!
Yes, & one remedy is said to be rubbing Vicks into the nail, & another is soaking in apple cider vinegar! So I’m trying both!
Tea tree oil is a good remedy for fungal nails and may help with this? I have recently had white spots which have turned crumbly so assuming a fungal nail infection, blaming PMR/Pred but who knows.
Can this be a sign of psoriatic arthritis? I am sure I read somewhere this can be one of the first signs.
I looked it up but I don’t have any other symptoms like psoriasis or arthritis so hopefully not
PsA can have a polymyalgic presentation! One rheumy was insistent I could have PsA - never had psoriasis (only in the family) and textbook PMR symptoms except normal range markers and only PMR-type joint symptoms but he was bent on it being an inflammatory arthritis. Time has shown otherwise I think!