Guest guest Posted April 29, 2010 Report Share Posted April 29, 2010 Hi Francine, I have heard of Dr. Alan Mentor. I used to live in Hurst and received my diagnosis of PsA when going to JPS in Fort Worth. Needless to say there wasn't much done for me there, so when my disability and medicare finally kicked in I got out of that. I went to an awesome rheumy in Bedford, Dr. Iman Ali. She mentioned him many times in the years I went there. He should be a very good doctor, especially if you are having problems finding a med that works for you! I can provide some insight on your questions. 1. There have been times I have gone to both a rheumy and a dermatologist. I am fortunate in that Remicade also helps in clearing up my psoriasis. I have pustular P on my hands and feet for the most part, but occasionally get the plaque kind on my shins and elbows. I usually go to a dermy for skin type infections. It really depends on how your rheumy feels about having to treat both. 3. Dovonex is a topical ointment that helps with psoriasis and a few other type rashes of that nature. I have Dovonex and clobetasol but have found that Dovonex works just as well by itself. Use Dovonex very sparingly though. It is Vitamin D and it will absorb through the skin. Also these type ointments can cause thinning of the skin and sensitivity to the sun. 4. It was probably the fourth treatment of Remicade before I really started to notice improvement, marked improvement. My gait before was as if I had been hobbled. It was after the fourth infusion that I noticed one day I was walking better. But it varies for each person as to how much and how fast any of the drugs work. Ultimately what you are aiming for with biologics is for the disease to go into remission. For me it is slowing it down a lot, but I still have flares of swollen joints on occasion. 5. I can't honestly tell you how long it will take for the flare of P to clear up or if it will. I know when I get an infection of any kind mine gets bad too. I always have a small patch on the outside of left foot that has never cleared up. I can tell you that with Remicade, Dovonex and a few other drugs that I am on, getting too much sun makes my P flare worse. I have finally gotten used to the fact that I will probably always look like a cast reject from Twilight, pale! LOL As for whether your post was too long or not, when you have questions by all means ask them! This is a really awesome group. I am sure others will have some advice and answers to offer too. Gentle hugs, Dalene Quote Link to comment Share on other sites More sharing options...
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