Do You Believe That Since You Been Here Writing Your Psoriasis, PSA Etc.. Stories And Sharing, Has Improved Your Psoriasis, Less Flares?
I know getting knowledge and hearing about how others cope with their struggles and what meds. they are on or tried us priceless to me, but if you are one who just reads here but doesn't really talk to others ( which is totally fine, I did did when I first came here 2). Do you see a better result in your personal struggles with Psoriasis or PSA ..etc.? I'm just curious.
Hi, according to Google "Psoriasis affects an estimated 7.5 million to 8 million people in the United States and about 125 million worldwide."
These are really scary numbers and just shows that no-one fighting this disease is alone!!! It also makes one wonder why so many doctors do not understand or know how to treat this disease which is even scarier!!!
Hope your day is better than average...π
Hi Don, you've been having crap weather and crap life in recent times, glad to see that you've been getting stronger in coping with your situation, health etc as best you can. God bless and may He give you strength!ππ»
Hi Don, I agree with Joanne - the fact that we can reach out to talk to people or vent about our problems does help with the depression and anxieties we all experience and cope with each day. Hope you have a good day!πΊ
I have PSA, scarlederma, and scap psoriasis. My pulmonolist, watches my heart and lungs very close he believes it is the scarlederma. I tend to think it's both. Rheumatologist says the only for sure diagnoses is PSA still working on more. I'm on oxygen as needed , I go for echo this week. . Lol I'm venting. I believe this group helps mentally. Family and friends don't understand.
Considering that I was the only one in school that had Ps, I thought that I was a freak. I was so surprised that so many people have some many varieties!
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