Mary:
It sounds as though you are describing
callusesCorns and calluses. Are you wearing footgear which rubs? If so, padding the skin may help.
To soften what's there, try a cream containing 20% urea. You can buy that over-the-counter in the drugstore.
Best.
Dr. R
These sound like calluses. Do they rub against something (if so, padding them with moleskin may help.)
For treatment, start with a cream containing 20% urea (OTC). This softens thickened skin very well.
Best.
Dr S
Ian, your wife's problem sounds awful. I hope you can find a solution for her.
This sounds like you are allergic to possibly Home Products that you use such as: Laundry Soap, Foam Baths and also food that you may eat. Putting Socks on at night will not help as it will overheat your skin, make it sweat, dry it and consequently make it worse. First off, it sounds like you have an advance Psoriasis on the verge to become cracking and bleeding. You must act at once and if you wish for us to help out, please, contact us at: " medals.***@**** " and it will be a pleasure to help you.
We are a Distributor of Natural Body & Home Care Product for a Company called: " Druide Laboratories Inc. from Montreal, Canada " and we have specialized in Skin Care of People.
Best Regards
Joe & Ghislaine
Our Web Site: " http://www3.ns.sympatico.ca/medals.cmms/ "
Hope it helps. Thanks for helping your wife. My husband doesnt say anything to me. I wish i had someone like you who understood with compassion. So i told him to get a new model wife without all the imperfections!!haha.
Karen
ps. if you notice Joe is on everyones message board trying to sell something. I hate that. I feel like i am a leper and they are trying to feed off of us. I have had so many people approach me with their snakeoil cures. They shouldnt be allowed on these forums to sell there wares. We are looking for personal help and compassion from someone that knows what we are going thru. Not some sales pitch. But of course the net is for everyone and allkinds.
Take care, He needs to go to a doc to slow this problem down.
Karen
thanks for the advice the glue sounds like a great idea , my wife (Larissa) is a bit unsure though .
It does seem like its hereditry, her sister ,mum, or mom as you call them and grandmother both have it on ther hands and feet
the conditions you describe are almost identical to the conditions on her feet, including difficulty walking and bleeding frequently . It does lead to self esteem problems as well .
Is Psorisis easily treatable or more a suffer in silence kind of thing? I will scan the archives and see what else is available
I know there are so many different snake oil type "cures" around I was having trouble finding information on line from any source with out bumping into that type of thing and their "miracle cures " Best of luck with yours as well
PS .I was checking the Derm forum daily , but with no results , I became despondant and hadn't checked for ages , I just thought i would check again -Im so glad I did . cheers Ian
Nice to see you again. Yes i say mom, you must be british to say mum. i am from canada.
Anyway, Psorisis is not easily treatible. I have got some info from a medicine package called Dovonex. It is a vitamin d cream made by LEO Pharma Inc. Maybe you can look up more infor about psorosis at their site. Seems to me so far it is not responding well. I wonder if it will ever go away. I have gotten used to the contant bleeding from cracked fingers. But i wonder about blood poisening from so many open cuts.
From what i have read so far, there is no cure and they are not sure why it starts. Great! But stress and heredity is their answer for all. I hope your wife is doing OK. I was so depressed from this i told my husband that i would leave him so he could get a wife that doesnt have so many medical problems. I am on meds now for depression. This skin problem is very serious to the lives around it. Effects all, work, cooking cleaning, holding hands with the ones you love is taken away from us. The little kids say my dry cracked skin hurts their skin. And wont hold my hand. For a mother this is very depressing.
Anyway, thanks for lettng me go-on-andon.
Take care,
Karen.
your situation sounds awkward I can understand why you must feel the way you do . fortunatly Larissa does not have it on her hands although her mother does .
How young are your children? they sound like they must be quite young . We dont have children yet Here is my address if you want to comunicate off the forum ***@****
My kids are small but not that small,(always babies to me!) I have a policy to never relay email to people on the net, but thanks anyway for the offer. I am sure you meant it with the best interest at heart.
I hope Larissa is doing ok with her hands now. It is getting to be summer here and is good for skin. The sunshine does good things for the whole body.
Must be going,
take care,
k
Ian
years and in my case the more i worry about it the worse
it becomes. Now when i have a flare up i just try to
keep my skin as moisteurised as possible and try to relax.
My brother & I take from my nother's side of the family, werease my other 2 sister's from Dad's side have no effects.
My treatment apart from topical coal tar based & shampoo (TGEL)which can be bought over the counter is very expensive but very good.I am also undergoing UV Light Treatment at my local Hospital for the second time and this is working wonderfully ( you even get a tan)care obviously has to be taken for fear of skin cancer. so you need direct medical advise and which light you may need.You can get this treatment on NHS in UK but you will need to be referred by your GP.
I feel lucky I do not suffer with it on my hands or feet but basically everywhere else.I used to wear trousers everyday so no one could see my legs, but you must get light to your skin as much as possible and to this I go forward and don't care.
Please I wish everyone who suffers great stregnth and happiness and keep your chin up.
See ya
Scott.
PS Psorisis doesn't like sunshine so 10-15 mins a day on affected areas helps as well and this came from the skin specialist. By the way you need a prescription from your local GP for the ointment and it costs about $20. And be warned DON'T GET THIS STUFF ON ANY OF YOUR CLOTHES OTHERWISE OUT THEY GO, IT'S STAINS REALLY BADLY.
I also suffer from Psorisis and have tried many creams, ointments etc with nothing really working all that well. I have found that the best solution is coal tar. I mix coal tar solution (2%) in with aquious cream and apply this to the affected areas on my skin. I also mix a bit of coal tar solution into my shower gel. I find that this does not eliminate the affected area but it does prevent further developement and iching. I buy the coal tar solution at a pharmacy without a prescription so it is fairly easy to get hold of (may differ from country to country). The pharmacy can also mix up the coal tar and cream for you. I have be told that Psorisis is genetic but is only transfered via females and that there is no known cure for Psorisis and that it can only be controled at present.
Cheers
Alex
I also suffer from Psorisis and have tried many creams, ointments etc with nothing really working all that well. I have found that the best solution is coal tar. I mix coal tar solution (2%) in with aquious cream and apply this to the affected areas on my skin. I also mix a bit of coal tar solution into my shower gel. I find that this does not eliminate the affected area but it does prevent further developement and iching. I buy the coal tar solution at a pharmacy without a prescription so it is fairly easy to get hold of (may differ from country to country). The pharmacy can also mix up the coal tar and cream for you. I have be told that Psorisis is genetic but is only transfered via females and that there is no known cure for Psorisis and that it can only be controled at present.
Cheers
Alex