Sun-13-11-2016, 04:07 AM
All my new dear friends!
I am so thankful for sharing with me your stories and experiences - i read all of them carefully and get some knowledge about the ps that i did not have before.
I am still in shock and reading internet too much, which is pointless now since i have you.
I am trying to accept my new condition, and it is not going so easy.
For example (ladies may understand me) - i was in pedicure salon today, and lady in the next chair started small talk with me and when she saw my rashes - she could not hide her disgust and stopped talking to me, and i fully understand her ..Thanks to the universe, my manicure lady believed me it was not contagious, and did her job as usual.
I deal with the new reality... You all know - it is hard...
My family supports me, my hubby even found a special psoriasis UV lamp, that we gonna try tomorrow, on my hands first - just for 30 seconds as instructed ( Jim did not approve this idea, but one-two tries should not harm, right?)), i hope it gets better, i have to go to the office mostly every day and contact to many people - don't want them to be scared of me..
About treatment for now - high dosage of cortisone cream, don't see any improvement yet, probably it's too early, and i need to apply it to almost everywhere on me except the scalp, half of the tube is already gone, i need a barrel ))
Thank you all again, and I wish you all the best.
Regards,
svp
I am so thankful for sharing with me your stories and experiences - i read all of them carefully and get some knowledge about the ps that i did not have before.
I am still in shock and reading internet too much, which is pointless now since i have you.
I am trying to accept my new condition, and it is not going so easy.
For example (ladies may understand me) - i was in pedicure salon today, and lady in the next chair started small talk with me and when she saw my rashes - she could not hide her disgust and stopped talking to me, and i fully understand her ..Thanks to the universe, my manicure lady believed me it was not contagious, and did her job as usual.
I deal with the new reality... You all know - it is hard...
My family supports me, my hubby even found a special psoriasis UV lamp, that we gonna try tomorrow, on my hands first - just for 30 seconds as instructed ( Jim did not approve this idea, but one-two tries should not harm, right?)), i hope it gets better, i have to go to the office mostly every day and contact to many people - don't want them to be scared of me..
About treatment for now - high dosage of cortisone cream, don't see any improvement yet, probably it's too early, and i need to apply it to almost everywhere on me except the scalp, half of the tube is already gone, i need a barrel ))
Thank you all again, and I wish you all the best.
Regards,
svp