juliesdreamteam
New member
Oh I see. So, while others post precautions of their centers, those post are not "irresponsible". While my posting a differing post is. The "life in a bubble" is a figure of speech used by the transplant surgeon. That is a fact. I'm assuming you weren't there for that conversation. I would sincerely hope that no one use this forum as a means to replace the educated transplant teams directions.
My response had everything to do with her original post. She asked a question about other's directions. You seem like an intelligent fella. Read my post again. Is there anything in that post, that would suggest a person should follow the same guidelines? Or could it be...just maybe....that I offered an account of a different personal journey?
I'll take another stab at this and draw it to a close. You may well be 13 years out from Tx. That is fantastic. I wouldn't dare be judgmental of a person I didn't know. I'll go out on a limb and say that I've probably done more to end this disease than many and you know shit about what pride this CF spouse has.
Continued good health.
My response had everything to do with her original post. She asked a question about other's directions. You seem like an intelligent fella. Read my post again. Is there anything in that post, that would suggest a person should follow the same guidelines? Or could it be...just maybe....that I offered an account of a different personal journey?
I'll take another stab at this and draw it to a close. You may well be 13 years out from Tx. That is fantastic. I wouldn't dare be judgmental of a person I didn't know. I'll go out on a limb and say that I've probably done more to end this disease than many and you know shit about what pride this CF spouse has.
Continued good health.