Experiences with

Athlete's foot

I’ve been using athletes foot cream for 3 weeks now and I don’t think it is that no more. There red spots and it only really itches at night. It also only effects that area hasn’t spread my partner hasn’t got it so that’s also why I feel like this could be something else. Thank you

I ,think I have athletes foot although having had ra for 10 years I am no athlete! I have been to gp,rheumatologist, dermatologist and podiatrist they all say that they can't see anything so dismiss it.keeps me awake, use cream and ice packs which eases the pain/itching but its no consolation.

He is being treating for athletes foot but it looks much worse than that and isn't improving after bathing it and applying his steroid cream. Had anybody else come across this please ?

past week I have had problem with both feet being hot in bed, theres no athletes foot etc, And I moisturise feet in mornings after shower, I know its one of side effects of hypothyroidism , anyone offer any advice ? Thank you

He has been receiving treatment for athletes foot and I have been bathing and applying steroid and anti fungal cream for months now, and it is getting worse.I am concerned it could be odeama. I think we need to understand how bad his liver has got now. Thank you

As I have dropped down my steroids (now on 10mg for the last 6 months) have had various foot issues from athletes foot to an impressively large wart (now gone) on the little toe, eruptions of eczema on the side of the foot or possibly psoriasis, dealt with by topical creams.

I have been struggling with the above since April thinking that was extreme athletes foot. But mentioned this to my rheumatologist who suggested a scan. The cardiologist diagnosed Mortons neuroma . Just wondered if anybody has the same thing and if there is any connection with R A?

However I have developed some mild fungal infections; Ringworm on Face, fungal infection on toenails, and start of athletes foot. Has anyone had more than 1 of these infections simultaneously and if so how were they treated ? Currently I’m treating them all separately as per GPs advice.

It’s gross but my second and third toes my affected side I have had athletes foot fungus that makes the toenail disgusting. I’ve read a book that It said that it’s very common for that to happen with Parkinson’s.

A newspaper article and a paper in Nature that raise questions about the effects of Proton Pump Inhibitors (PPI - such as Omeprazole, Lansoprazole, Dexlansoprazole, Esomeprazole, Pantoprazole and Rabeprazole), Sucralfate, H2-receptor antagonists (such as Cimetidine, Ranitidine, Famotidine, Nizatidine

Has anyone experienced increased allergies with Hashimotos?? My wife has had it for 15 years. she had the vaccine for covid last year and now seems to be more allergic to anything from her favourite food to glasses she has worn for years and eye drops she has used for the past 3 years with no probs

He has though developed horrific thick dry skin on the soles of his feet - never had anything like this before - treated as if it was a random athletes foot but no evidence of infection now ( from my limited knowledge ) but painful thick skin that is peeling slowly.

Doctors not sure could be shingles, athletes foot, a skin infection or covid!? Thanks in advance

Several rounds of antibiotics this summer. Had some small bleeds. Bleeds have stopped. Done with antibiotics. But I’ve been having noise in my chest. when I lay down at night. I Think it’s from all the mucous I have draining. Pulmonologist said my lungs sound good and ct scan looked good. I’ve had this

I've had athletes foot for as long as I can remember. Decades. Mostly on my left foot and is manifested by the usual insane itching between and on tops of toes and over the years my toenails have become thick and brittle. Again only on one foot.

Just started for the first time predosolone 5 mg once daily for a month ( summer in Greece you see:) and i had an athletes foot for some time now. Does it get worse on steroids? I forgot to ask my doc although he claims that the dose and time is too small to actually make it worse.

It felt either athletes foot or if my toe nail was catching the skin. It would only come every few weeks or months. I thought maybe it was my footware or because I had been on my feet for along period.

After my last couple of posts, I have come to the conclusion thanks to all the lovely people in here that I should probably check myself for food allergies so I have ordered the smartblood food intolerance test (only the 1st step though)... Although I am almost certain I have no allergies it would be

First, in trials as a cure for (I think) athletes' foot, it was never marketed for that because it was a powerful immune suppressor.

Looking back, it is difficult to remember all my medical conditions which have improved, largely through IF - so I made a list: The bottom right photo is recent Toenail fungus - bottom left Athletes foot Peripheral oedema Peripheral cyanosis (blue foot disease) bottom right.