----------------------------------------------------------- New Message on Pituitary Chat
----------------------------------------------------------- From: JPShaw55 Message 1 in Discussion My prolactinoma was rx'd in 2001 and I started treatment on 9/11 (yeah, who'd forget that). It's been pretty consistant although I'm on cabergoline because my insurance knows best. My question is, are there any other men out there with long term experiences? I get twitches when I rest, still don't have enough energy, and am wondering if the steady treatment is losing effect. I have an appt with an endo this month. Since I have the world's crappiest insurance it's taken about five months to get this. Very few endos take my ins. Anyway, I'm holding out hope that I can get back some of the energy I once had when I first got treated. I had an MRI about 3 yrs back. My pit tumor had shrunk from 1.2 cm to 6 cm. But still I don't do well. I also take androgel daily. Jim ----------------------------------------------------------- To stop getting this e-mail, or change how often it arrives, go to your E-mail Settings. http://groups.msn.com/PituitaryChat/_emailsettings.msnw Need help? If you've forgotten your password, please go to Passport Member Services. http://groups.msn.com/_passportredir.msnw?ppmprop=help For other questions or feedback, go to our Contact Us page. http://groups.msn.com/contact If you do not want to receive future e-mail from this MSN group, or if you received this message by mistake, please click the "Remove" link below. On the pre-addressed e-mail message that opens, simply click "Send". Your e-mail address will be deleted from this group's mailing list. mailto:[EMAIL PROTECTED]
