My family doctor and my cardio therapist have asked why I am not on a transplant list. I have to never thought about that and my doctors have never mentioned it.Has anyone on here had a long transplant and how are they now?
Lung transplant. : My family doctor and... - Lung Conditions C...
Lung transplant.
oioi i had mine 11 03 2016 thats when my new life started i wld always say have it done id do it all again if i had to its brill i can walk now take me dog etc anything you want to know plz feel free to ask
Do you think you'll recover enough to go back to work? I'm ok if I don't get that well but I want to be well enough to take walks and possibly not need oxygen.
im nearly 60 and was a butcher so no cus of immune sys is so low now im not planning to i took ill early ret and with what ive been throu i want to enjoy life a little i so very nearly lost it but some do ive met them at clinic you need to be a little younger than me i think
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Thank you. Didn’t know that. 😜
I've been on the active list 15 months now, I got called up last month but I was just stand by so I didn't get it but I put it down as a good experience. My consultant had been asking to refer me for transplant for a couple of years before I agreed to be assessed. I wish I had earlier because I feel my deterioration. You should get assessed and then make your mind up.
That is what I was thinking I should do. Thank you for the extra confidence that I should do that. I was really sick in 2012. I've improved about all I think I can. My mother, who is in her early 60's gets around better than I do. I've been pretty accepting of my condition. My therapist says I'm too accepting now b/c I'm 43 and should be living life better than this. So thank you, I see my pulmonologist November 2nd. I will see if she will refer me for a evaluation.
Unfortunately I found out and it was confirmed when I went up to the London Hospital in Feb this year that if you are over 65 the chances of getting a transplant are zilch, eg your to old. So that's me, why I wasn't told this back in 2004 when I was diagnosed with Alpha 1 is beyond me, but there you go. Now there is nothing they can do for me. Yep, I will continue with the puffers, tablets and Oxygen to give me some quality of life, but I will slowly deteriorate and then pop my clogs. So if you are under 65 and have COPD get your name on a list ASAP for a transplant and don't get put off. In case you are wondering I am a non-smoker so the word fair is always prefixed by un, but that's life
If it's bring suggested, get on the list as if you wait until your 65 you are classed as too old and you can't get on a list. I was told this in Feb this year up in London, and I am now 68. You would have thought I would have been told back in 2004 when I was diagnosed, but no. Green rub. Also add I am a non-smoker, so double whammy. Life is not fair so if you have COPD take what ever is being offered and ask for everything. In fact demand as its your right