MarLinTX if you have a hematologist why not ask those questions of him/her?
I do run things by my hematologist - ex: when I had total knee replacements 9 months apart I checked with him first about the daily baby aspirin I'd have to take to keep away blood clots.
What is your count? What treatment, if any, are you using?
I know you are scared - but let me tell you about my experience. I was diagnosed in 1989 a couple months before we were to move to Tokyo through my husband's job - I was given the opportunity to cancel the move but I felt this was an opportunity of a lifetime and didn't want to give it up for my husband's sake and also our sons. We moved while I was on 60mg of prednisone and not knowing if I would have a hematologist or what. Turns out I had a super hematologist in the Japanese system AND he knew my hematologist here. I am so thankful we moved and had the fantastic experience we did - also moving from Tokyo to Hong Kong and traveled to different countries and I didnt' even check my count first. I did stay on prednisone, but lower dose, while overseas and got off it when we moved back. We were there almost 4 years - since back we have traveled overseas and within the States - I've given up only skiing because I like my bones the way God made them.
I was given the opportunity to have my spleen removed but since they could not assure me I'd be cured I have kept my spleen.
This is all very new to you and I do sympathize - we are here for moral support and to share our experiences with you. I may be one of the lucky ones as I've had ITP for almost 33 years now and have had some setbacks but nothing too bad. My count isn't in the normal range and really the hematologist doesn't want it there - it did go up however while on the baby aspirin which was a surprise.
Take care now - keep us posted and don't give up!
"Instead of wasting your time worrying about symptoms, just get it checked out" -Nieca Goldberg, MD