+ Reply to Thread
Results 1 to 5 of 5

Thread: Palmar-Plantar Pustular and Acropustulosis

  1. #1
    Join Date
    Mar 2005
    Location
    Ohio
    Posts
    11

    Question Palmar-Plantar Pustular and Acropustulosis

    Anyone out there have one or both of these conditions. I have had (wrongly diagnosed and treated) acropustulosis on my finger tips and toes for my whole life and have recently developed PPP on the bottoms of my feet and the palms of my hands. I don't like the idea of taking Embrel. What have you tried that helped ease the pain and/or speed recovery?

    Also, what do you think of parafin dips like you can get at a nail salon? Helpful, hurtful, no comment?

    ANNA

  2. #2
    Join Date
    Jun 2004
    Location
    North Carolina
    Posts
    8,885
    Hi Anna,
    I have Pustular Palmar-Plantar. Enbrel did not help me and I had a horrible flare when I stopped it. It is just a chance you would have to take. What helps me the most is staying off my feet. I use a wheelchair or a scooter a lot. That really helps with the cracking skin. I also use Lidoderm patches and Thermacare Heat wraps.
    Right now I am taking MTX to try to calm down what Enbrel did. I am seeing some improvement. Hopefully, I can calm down and get off MTX eventually.
    It is a hard thing to live with. I have had it for 40 years and the worse time I have had was when getting off Enbrel and a long time ago-Prednisone.
    Go to my album to see why I have "HAPPY FEET"
    An antibiotic keeps my PPPP under control.

  3. #3
    Join Date
    Feb 2005
    Location
    Rhode Island
    Posts
    821

    parafin dips

    I have a home unit that I use, first I rub on tons of moisturizer then dip( it's a bit uncomfortable at first quite warm) three layers of wax then wrap in the baggies that come with it- sometimes I sleep with them on- My daughter loves the dips even though she dosen't have P- We make it a ladies night!! It is easier if you have another person to wrap your hands in the baggies. Then we sit around a giggle at how silly we look!

    When I had my first outbreak as a child (was diagnosed as Athletes foot) I soaked my feet in Potassiun Permanganate which dyes your skin brown- so I wore socks all the time to hide that-I can remember playing twister with friends and being the only one who wouldn't take off my socks
    Carol

    "Love is the lesson; Life is the school"

  4. #4
    Join Date
    Mar 2005
    Location
    Ohio
    Posts
    11

    Thumbs up Thanks "Grannie"

    I have used Ultravate for years and kept it wrapped--it was only on my finger tips and toes at the time. My doc gave me Elidel which did nothing. When the pustular stuff started showing up on my palms and then the bottoms of my feet I got freaked out. It took a while to get to the new derm, but I think he is going to help. He put me on an antibiotic, Dovonex ointment and something that starts with a C that I cannot remember at the moment. They feel better--I guess we will see soon.

    They advised against the parafin dips until my skin is healed. I have to agree at the moment. I think I am going to go back to the tanning salon for a few minutes a couple of times a week now that my hands are showing signs of healing.

    ANNA

  5. #5
    Join Date
    Mar 2005
    Location
    North Carolina
    Posts
    10
    I have acrop. Right now I'm getting ready to switch from methotrexate to cyclosporine. They haven't even mentioned parafin dips or uv treatment. Enbrel was mentioned, but my derm said they would rather I go for the cyclo. because enbrel wasn't tested on my type of p.

+ Reply to Thread

Bookmarks

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts