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that's not very helpful if you can't remember what the lotion was lol
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Erik, what was the point of your post if you can tell us the name of the lotion you used? This didn't help us one bit!
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Mike-sco, it is NOT life long. Mine went away for 2 years until I started drinking alcohol again.
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Can anyone elaborate how DPU progress.Does hives come out after itching?Does anyone experiencing burning sensation in palms? Does hives in palm and sole are visible?Can anyone explain how this progress?
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hey all, I had my o&p test come back positive for entamoeba coli cysts. Currently drinking wormwood tea.
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DAPSONE DAPSONE DAPSONE DAPSONE!!!!!!!
I can't emphasize it enough. I struggled with it for years, missed work and even had to quit a job because it caused too much pain and swelling), i couldn't perform. Most doctors didnt even know what it was. Im just an engineer with minimal understanding of human biology but after years of misdiagnosis and anti-inflammatorys, antihistamines, steroids, and other meds i did my own research (i know doctors hate this) and brought my issue to a dermatologist. After saying she'd never heard of it she sent me home disappointed, again. A few days later she called me back and said she did some research and said I did indeed have delayed pressure urticaria.

Long story short she perscribed me Dapsone. After a couple weeks my symptoms completely dissapeared. After 6 months I stopped taking the medication and have next to 0 symptoms. I get it a tiny tiny bit in feet and mouth but its usually just itchy with no swelling.

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Hi Mohammed, Thank you for your post. I know that I have Lyme Disease and within the last two years have developed DPU. I would be very interested in the name of the Dr. in Toledo that was able to help you. Thanks very much!
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Do you know the name of the lotion?
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Was the lotion you used a GoldBond product? Lotion or cream?
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Does anyone whith DPU also suffer chronic sinusitis? I have DPU for 4 years, I blame my chronic sinusitis which I suffer for many years.
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usually my DPU contolled by cetirisine and loratadine, but when I get ill (like cold whith higth temperature) in beagin of illnes DPU release me (and I can live whithout medicine for a while), but to the end of illness (when cold getting better) DPU get mad, and I need to rise medicine intake for 3 or 4 time to stop DPU. Does anyone who else experience that ?
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Totally agree ... I have had DPU for 18 years ... the only time I ever felt normal was taking the prednisone but all that did was damage my kidneys ... so I had to stop .... what solutions do you have ??
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So what was the name of the lotion
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any new suggestions people ? suffering from 10 years nothing helped

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