Wilkes Barre PA support meeting Dr T April 2008
 

Di...sounds like a great idea. Please post the info once you know. I am definately interested. Thanks.

Great idea! I would love a set of TOS videos from Dr. T. I have a friend in the movie business. Perhaps I can find out if he knows anyone who makes DVD's (assuming Dr.T is interested in doind it).

That sounds like a great idea and for a real toser to be in it and talk about the range of symptoms because from the information out they sure don't talk about the real symptoms that we go through i really think that is important because for a long time i thought there was something else wrong till i found this sight and found out that there where many who had the same systems as i did but were no where in the articles.

I might be able to attend if it's first week in april, tuesday or wednesday. It's a long drive from atl.

would LOVE to be there!

What a great thing ! I would love to attend ( I live in Mass. ) but I think too much driving right now. But I would definitely be interested also in the tapes !

What a great idea and gathering !

Dolfinz

I would love to come. I have been doing too much driving lately. Back and forth from FL and this weekend to Rhode Island visiting a college with my daughter. I could come and spend the night. I remember the Best Western had decent rates and was close. They also have a pool which might be nice for some of us. Maybe we could even do something there and get special rates. They used to give special rates whien having hospital appointments at Geisinger. Keep me posted. Linda

Wish I could be there! If I could make a suggestion though... any information and/or knowledge Dr. T could share or include on venous TOS, blood clots and vascular issues related to TOS, I would appreciate it!

As most of you are aware this is the rarest form of TOS and so there is just not a whole lot of information out there about it. What I would love to see, from any doctor anywhere, is a study on athletes and venous TOS, their diagnosis, prognosis, recovery (sucesses and failures), etc.

When I was first diagnosed and I got home from the hospital, I of course looked up this rare condition online and couldnt really find any information. It was awful to feel so alone and in the dark about the whole thing and just had to rely on what my doctor told me.

One day, I hope that there will be 100% credible information and in depth studies readily available to all TOS patients.

? cd?
 

I wouldn't mind paying for this info either. Even an audio recording of the meeting, via podcast, CD, Video tape, DVD, BitTorrent, etc...