Grover's Disease: What works to help find relief?
I have been diagnosed with Grover's disease under my breasts. I had a biopsy for diagnosis. Tried topical ointment with no really good results. Any ideas?
Interested in more discussions like this? Go to the Skin Health Support Group.
I’m a member too on the Grover’s forum and it’s the best for information. Googling brings up a lot of info but not necessarily accurate compared to this forum. I did start the cilantro (have tried about all the recommendations and some may help and then stops helping and others don’t help at all - right now witch hazel and gold bond medicated powder is helping the best) actually ate the fresh but after a week got tired of messing with it keeping it fresh and smiling with green bits in my teeth. Decided to do the capsules and it’s been a couple weeks, so far my itching and the rash is not as extreme as it was so maybe it’s working? I know many say it could take weeks/months to see results so I’ll keep taking for another month. 🙏
300 mg at night & 2 100mg as needed during the day got rid of my itch entirely for the last 8 months. I weaned myself gradually off the Gabapentin.
I also use 3 creams. 2 are steroids (Triamcinolone & Dexa “something”. The third is CETAFIL cream from the drugstore. I try to use the OTC mostly. I have been itch free & sleeping through the night. 😊
I’ve had it since June of 2022. I have learned that somethings work for me but not others and others and not me. The steroid cream stopped the itching while using to times a day. But now only works for about 4 hours. Tried other over the counter creams, that worked great for a week , but now doesn’t work only for a hour. Was doing the cilantro smoothies. But now doing the cilantro capsules. Much easier. Not seeing anything yet with cilantro, but going to give it a month. Some foods do make it flare up. Shellfish for sure on me. Heard about Retinal and tried some my wife had and it worked really good, so I ordered cream with a bigger % than what she had to see what it will do.
So it looks to me, that you need three creams to switch around so your body doesn’t get use to them. Steroid cream just for emergencies, because my dermatologist said it could cause other problems. Don’t know what they are. With all this I still have a bunch of bumps on my lower back middle and upper back middle. And I’m still getting them in other places, legs, arms, and feet.
Steroid creme causes thinning of the skin and should not be used longer than two weeks first month and then if needed only two weeks next month. Once your skin starts thinning you’ll never get it back to normal so use sparingly and cautiously.
After 1 yr. from having a stem cell transplant for NHL, I started developing red pustules underneath my breasts, which were very itchy and annoying. The biopsy confirmed that it was GD. I tried everything that people are chatting about (i.e. steroid creams, etc.). However, never tried light therapy or herbs. All I can share is what I have found which works for me.
I noticed after using a cream called “Skinfix + acne 2% BHA acne spot treatment”, (also contains Azelaic Acid which I purchased from Sephora for $30 - .05 fl oz., it reduced the red spots and itching after one application. - used it for 4 consecutive nights after showering. I will always get breakouts, but this product has really helped me tremendously. I suggest you confirm with your doctor if this is a product that can be used for your condition. Good luck!
If you have severe itching, you should beware of the drug ibuprofen and also suspect any other drugs you may be taking. Years ago I broke out in hives on my torso that drove me crazy. It took a while for me and my doctors to realize that the itching was a side effect of an NSAID Rx that I was taking for arthritis. I am allergic to the ingredient ibuprofen that is in all NSAIDS. Even Voltaren, which is a topical version of ibuprofen, eventually gets into my bloodstream and causes itching on parts of the body far from the joints on which it is rubbed.
Thanks for the information. I rarely take ibuprofen. I do take two Tylenol Arthritis every day. I'm pretty sure I also took them during my 13 years of not itching. Which is also the case with most other medications and supplements that I take. Good for you if avoiding ibuprofen helps. I have tried many of the remedies that help other sufferers to no avail. Sometimes I wonder if the transient nature of this scourge doesn't fool some people, including me, into thinking they found something that works.
I took 300 milligrams of gabapentin every night for 13 years and, to my knowledge never had any side effects that were noticeable. Somewhere around August 2021 I slowly started itching again. Makes me wonder if it ever worked and if my disease was just dormant for 13 years. After all, I had the red spots and a biopsy of Grovers for 15 years before I started itching.
Hard to tell, for sure. I’m just doing lotion now - alternating between OTC & steroids.
I’ll stay off as much medication as possible as long as my Grover’s is in remission.
Thanks for the reply. Good luck.
Has anyone experienced an itchy scalp from Grovers? If so, have you had good experiences with a shampoo/ conditioner that relieves the itching? Thanks!