Beth's Story

I have PV & have been in remission since 2003 after battling active lesions for 10 months.  With this writing I do not intend to trivialize anyone's situation, nor do I want to offend anyone by my experiences or ideas.  

Diagnosis: My lesions began early in October 2002.  I started with a blister on my chest that itched, became an open sore the size of a silver dollar, & wouldn't go away.  Late October 2002 I finally went to my PCP who treated it as an allergic reaction to something I came in contact with.  When that didn't work he treated it as this allergic reaction which had become infected.  I went back & forth to 6 PCP office visits with allergy creams, Cortisone 10, & antibiotic creams.  I was finally referred to a dermatologist in March 2003 & within days of meeting with the dermatologist I was diagnosed with PV.  At this time lesions also began to appear on my stomach and back.   I feel my case was mild since at a given time I never had more then 10 lesions at once.       

Treatment: My dermatologist put me on Augmented Betamethasone .05% Ointment.  My PV specialist put me on 2000mg of Tetracycline & Clindamycin 1% Gel.  I tried also tried OTC stress tabs with zinc but had to stop after only a week as they made me nauseous.    

Triggers: I believe my PV was activated due to an over abundance of stress in my life at the time.  In October I was planning a trip, selling my house, arguing with family, planning a party, and helping parents move to another state.  I did this while maintaining a marriage and working full-time.   

Additional Treatment: Since I felt my PV was activated by stress I decided to seek therapy/counseling.  With a friend's recommendation I met with a therapist that specialized in anxiety disorders.    I met with this therapist about 6-8 times.  The therapist gave me a relaxation cassette tape that was especially made for me.  The tape contained issues that I was dealing with and helped me relax.  I listened to the tape every night when I went to bed for about 4 weeks straight.  I would do whatever I could to beat this thing as the itching for me was unbearable & made my anxiety worse.  I did notice a huge difference after the 4 weeks.     

Remission:  In August 2003 my PV specialist told me that I no longer had active lesions and would not have to return unless I had another flare.  2 months after seeing my specialist I returned to my regular dermatologist who said I should take 1000mg of Tetracycline for another year.  Since this stuff also made me nauseous, I stopped taking it after 4 months.   

Staying in Remission: My specialist & dermatologist want me to stay out of the sun.  But that is difficult for me as I use the sun as my stress release.  I live in PA and for about 5 months out of 12 I get to use the sun as my solar power to recharge my batteries.  I do use 30+SPF while in sun.  My favorite thing to do is come home in the warmer months after work, sit outside with a good book & just feel the warmth of the sun.  To me it is calming.  I also avoid stressful situations.  In 2005 I was in the middle of a family argument which brought out about 4 blisters on my chest.   I immediately removed myself from the area and went with other family members to vent about the situation.  Sitting & talking calmed me down.  The next day the blisters were gone & the only evidence remaining was just a little redness in the area.  Since then I've learned to remove myself from any stressful situation.  This even includes preparation for the holidays.  If I find myself becoming overwhelmed, I let everyone know I won't be hosting anyone for the holidays, having dinner quests, buying gifts, etc.  If they do not understand my reasons, then they are just not worth my efforts anyway.  So far everyone has been more then understanding & supportive.  I find that even today, if I still feel stressed or anxious, I pop in the cassette tape for a few nights.  I believe this has also has kept me in remission since my last meeting with my PV specialist.    These are my own experiences.  Each person has their own battle to fight as each of us is different in our experiences, triggers, medications, etc.  

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