Pompholyx.co.uk

I suffer from pompholyx. So do lots of people it seems. Having spent many years reading about pompholyx on the internet, I decided to gather together the things I have found out onto one site. It seems that I am not suffering too badly – occasional quite lengthy bursts of itchy tiny blisters on my right hand and a few on my left. Other people suffer more – they get more on their hands, the blisters can join together and some people get them on their feet.

This website is meant to help people who recognise the symptoms and want to know what the heck they are suffering from. It's also meant to reassure people with pompholyx that they are not alone – they are not the only people to have the illness and that you can live with it.

Most of the site has been written in layman's terms – I'm not a doctor. Because of this I hope you will be able to relate to it more. But also, please note that if you think you have pompholyx or if you have any kind of skin complaint you must not self medicate. See a doctor or a dermatologist. They will know how to treat your version of the ailment.

If you have any comments or want to share your story about living with pompholyx, please do get in touch and share your experiences. Use the contact form to tell us about your experiences of pompholyx here.

Thanks for reading the site. I hope it helps.

This site provides you with some basic information about Pompholyx and the issues that arise from living with the ailment. If you want to do more research or if you want to know about treatments for Pompholyx and eczema we recommend searchig on Google.

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