Newly diagnosed, told to take MTX, help!

[ShaneM]

Thank you Caroline and thank you Jim. I have certainly noticed this is a friendly place, and after waking up thinking about it last night, it is a very calming place to know other people that have unfortunately adopted psoriasis and can talk through their experiences. I am generally a very positive and strong person, but sometimes you just need to see people are doing well with it to keep you going, especially with it being a new thing. I am now getting used to the idea that I have psoriais is now. 

So Jim, with your experience with MTX, did the psoriasis come back when you stopped? I have also seen it comes back with a vengeance? Do you also know how long you should take these tablets for, or are the indefinitely? I'm sorry for all the questions, my doctor was very vague! I am also working my way through the site for answers.