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Peggy
Member
Username: Pjr51

Post Number: 2
Registered: 07-2013
Posted on Tuesday, July 30, 2013 - 11:57 am:   Edit Post Delete Post Print Post

Hi I have pulmonary fibrosis and am confined to the hospital at the Cleveland Clinic. Just found this site so thought I would join. I just got the word yesterday that I am on the list. So now I just have to wait for the gift of new lungs or lung. I feel hope for the first time since my diagnoses.
Jay Lackritz
Forum Leader
Username: Jay_ny

Post Number: 552
Registered: 01-2007


Posted on Tuesday, July 30, 2013 - 02:23 pm:   Edit Post Delete Post Print Post

Congratulations, Peggy.

I had my double lung transplant in New York back in 2007, and I am one happy camper!
Couldn't breathe, couldn't even walk much before my transplant, and was told I had less than 2 years left to live. I was lucky enough to get a double had haven't looked back since. Had some minor bumps in the road over the last 6+ years, but I am doing great.

Hope your wait is not too long.
Jay Lackritz@Optonline.net
Jay Lackritz.com
Bilateral Lung TX, May 10, 2007, Columbia University Medical Center/NYPH
Google doc
Google doc
Jack
Forum Leader
Username: Johnhollenbach56

Post Number: 591
Registered: 12-2009


Posted on Tuesday, July 30, 2013 - 03:14 pm:   Edit Post Delete Post Print Post

Congratulations Peggy, may your wait be short and recovery swift and 'bump-free'. Please feel free to ask any questions you may have - there are plenty of folks here who have already gone through what you are (and there is no such thing as a stupid question).

Stay well
Jack Hollenbach
Received double lung transplant August 2 & 3, 2007 for COPD at UCSD Thornton Hospital, San Diego, CA

Live each day to your fullest, for it is a gift to be treasured
Hostess Risé
Board Administrator
Username: Rise

Post Number: 17798
Registered: 05-2003


Posted on Tuesday, July 30, 2013 - 05:57 pm:   Edit Post Delete Post Print Post

Welcome Peggy to Transplant Buddies
I wish you the best with your road to transplant. I hope you will stay with us and contribute your thoughts and feelings.
Have you visited our sister site http://transplantfriends.com
CF- dx at 2yrs. 2nd double lung tx-05 JMH
My Photos on Transplant Friends

Facebook-TransplantBuddiesfriends

Twitter-transplantbuds

Contact: transplantbuddies@gmail.com
LadyDi
Forum Leader
Username: Ladydi

Post Number: 2810
Registered: 03-2008
Posted on Wednesday, July 31, 2013 - 08:40 pm:   Edit Post Delete Post Print Post

Congratulations Peggy! May you have a short wait!
Kidney Donor to Husband 10/30/07
Forum Leader-Living Organ Donation
Barnes Jewish Hospital St. Louis, Mo

My Donation Story

Post Donation Things to consider

I walk slowly, but I never walk backward - Abraham Lincoln
papillonbleu
Forum Leader
Username: Papillonbleu

Post Number: 2258
Registered: 10-2007


Posted on Thursday, August 01, 2013 - 06:44 am:   Edit Post Delete Post Print Post

Welcome Peggy! It is marvelous to hear that you have now made it onto the list. May your wait be short, and may you be able to keep up your strength and hope as much as possible until that time and beyond. Best of wishes and many hugs.
Bobbiejo
Forum Leader-Multivisceral
dx: GERD 1995, gastroparesis 2002, pseudo-obstruction of the bowel 2004
multivisceral transplant, 6 organs, 10/06/05
University of Miami/Jackson Memorial Hospital

DAP1122
Forum Leader
Username: Dap1122

Post Number: 3465
Registered: 05-2008


Posted on Monday, August 05, 2013 - 07:04 am:   Edit Post Delete Post Print Post

Congrats on being listed Peggy!!

I volunteer at CCF each Wednesday, so if you need a visitor, just let me know where you are located and I'll stop by. I'm a heart recipient, but I see many lung transplant folks on floor J-8-2.

I wish you a short wait.

~ Don
New blog/web page -
My2ndHeartBeat
Dap's Email

Heart Tx - 5/11/2007
DAP
Ohio, USA

Join our Transplant Buddies Calendar

Don's TransplantBuddies Blog

Google+ ..... gplus.to/NewHeart
Rita
Forum Leader
Username: Rita

Post Number: 940
Registered: 06-2003
Posted on Monday, August 05, 2013 - 02:52 pm:   Edit Post Delete Post Print Post

That is wonderful you are on the list. I hope it happens very soon for you!
Rita
Kidney Transplant 9/95
New York Hospital, NY
Dr. Wang

Rita's Page on Transplant Friends- see her photos

Lessons of Hope, Love and Kindness blog
Paul
Member
Username: Paul_palmer1963

Post Number: 4
Registered: 01-2014
Posted on Thursday, January 02, 2014 - 08:18 am:   Edit Post Delete Post Print Post

Hi im tim, ive got chronic rejection. Lost 25% of lung capacity over a 12 month period... change of tablets did not work so they are now arranging radiation treatment in February.

i just would like to know if anyone has any advice to offer on radiation treatment.

also should i carry on with my job as a plasterer? Regards
Hostess Risé
Board Administrator
Username: Rise

Post Number: 17965
Registered: 05-2003


Posted on Thursday, January 02, 2014 - 09:14 am:   Edit Post Delete Post Print Post

Hi Paul
I am sorry to hear this news but if you are stable that is a good thing. What does your doctor say about the work that you do. I do not like being around chemicals. What does your job entail?
Where are you from? Please return to update us. I hope all goes well!
CF- dx at 2yrs. 2nd double lung tx-05 JMH
My Photos on Transplant Friends

Facebook-TransplantBuddiesfriends

Twitter-transplantbuds

Contact: transplantbuddies@gmail.com
Paul
Member
Username: Paul_palmer1963

Post Number: 5
Registered: 01-2014
Posted on Sunday, January 05, 2014 - 02:59 pm:   Edit Post Delete Post Print Post

Lung capacity is still losing ... Im just crossing my fingers with regard to the radiation treatment but cant seem to find much information on it. Im self employed but the doctors will not commit themselves as to whether i should stop working. Just wondered if anyone else had any advice.

I am from the UK

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