Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum. ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
I have used over the counter anti-biotic ointments but it hasn't helped other than to act as a lubricant, much like Vaseline. Everything seems to aggravate it including stress.
I was told that much like any other exczema or dermatitis, no known causes or cures.
Every explanation I've read has been vague at best. But let me know how the culture thing goes. Even if I never get rid of it I'd find some consolation in knowing the cause!
Connections?
has anyone noticed their fingernails grow really fast with an outbreak?
i have never had an outbreak on the outer side of hands..only where the sun doesnt fully reach..on the palms and inside of fingers i was thinking light therapy may help a uv light? anyone tried?
Tried everything...biopsie, test of allergies, bloodtest, etc...
Every doctor and dermatologist in Belgium I have visited.
No doc ever called it that whay.
Till one... he knew directly a cure: he prescribeded me Prednisolone, corticosteroids and I was treated by that doctor 3 times a week with UV-radiation. I had to put a verry fat layer of cream with lots of ureum (urea) I guess in it on my handpalms and foot soles and then take place in a UV cabine for a few minutes. This was the only method that had result. But I stopped with it because due of the cortico's my haire felt out...etc.
I lived with it for so many years now... I don't want to poison my body all the time taking cortico's etc... and now my hand are back peeling all the time...!!! frustrating!!! (sorry for the spelling mistakes) greeting to all
Please note that any medically related information provided in this report/advice is not intended as a substitute for advice from any registered physician or other healthcare professional. Whilst I have endeavored to ensure that all information provided in this report/advice is accurate and up to date, I take no responsibility for any error or omission relating to this information, nor any responsibility for what any person may or may not do as a result of reading this report/advice.
I am a 50+ year old male and have had the condition Exfoliative Keratolysis (EK) for over 35 years, and have tried most if not all (cures) – Doctors, Dermatologists, Naturopaths, Herbalists and several ‘Theorists’. Have been researching and experimenting with my EK for over 30 years. My parents were in medicine, and so I had some inside knowledge and access to research, although a lot of it (some unqualified) is now available on the net. I don't know everything, but I do know what works for my EK. I believe that EK 'management' is really a matter of trial and error – unlike some medical conditions there is no ‘penicillin’ type cure (yet).
The following is a brief summary of what works and doesn't work for me, and my thoughts on EK. I am providing this in the hope it may help some others.
The first step I had to make was to accept that my EK condition will not kill me, but it is something I have to live with and have to manage myself. In my experience there is no miracle pill/lotion/cream I can get that will cure it, and there is no plant growing on Mount Himalaya or in the Amazon Jungle that will either. Some things make it better for a while, but there is no permanent cure - although it does run its course and 'go away' in some people. My advice to others is to accept this, then you can find out what works for you and then implement a management regime (and change if needed, and try new things sometimes). Maybe this will result in a cure, and maybe it may last a lifetime.
My hands do not blister - they used to, but they have not done so since the condition started many many years ago. I believe that this lack of blistering and some associated problem with the natural healing processes in the particular skin type that EK affects, is the core of the issue.
At its worst my hands would be completely 'stripped' of 'good' skin - the fact that I used to play so many bat and ball sports did not help (life is too short). I wish I had learned my management regime a lot earlier - but that's how it goes.
My EK gets worse when the weather is hot or after periods of excessive hand contact activity (eg hammering nails, fixing cars). In winter where I live now, it gets down to -10C (15F) and my EK all but disappears. If someone was to go somewhere really cold for 2-3 days and expose their hands to the cold, and if they get better and the EK dissipates, then they on the same page as myself. I believe the cold helping is due to the healing process working better when the skin temperature is lower and less moisture is lost than when the skin temperature is high.
EK is not due to stress - but stress can initially bring it on (it would come sooner or later anyway) and stress can make it worse.
Topical steroids/cortisone and injections are not the answer for me - they 'repair' the damage, but EK always comes back (sometimes worse). There are many other prescription drugs and natural options/cure available, and for me they all do the same. Going down this path lead to a cycle of repair and damage, but no cure. However, I have learned that EK may 'burn out' for some people who take this course of action.
The EK condition is somehow related to moisture loss in the specific epidermis layer of skin that is only on two parts of the body and the natural healing mechanism of the skin. I believe that this is why EK is only on the hands and sometimes on the feet. The skin on the hands and feet is unique and is designed to be damaged and to heal quickly. To counter the problem, I keep my hands moisturised, avoid damaging my