About Me

Were you a member of our Forum on http://TransplantBuddies.com


Where did you hear about Transplant Friends?

I found it while searching for transplant stuff on Google.

Are You Male or Female?


Share - which illness led up to you needing a transplant?

Cystic Fibrosis

Which Organ(s) did you receive? If you are on the waiting list, please share.

Recieved double lungs and liver

How many years have you had your Transplant for?

Since November 30, 2012.

I am Interested in Transplant Friends because...

I want to share my experience because not many double lung and liver transplants have been performed yet. Plus I want to read other peoples experiences.

Which Transplant Center has or will perform your life saving surgery?

Methodist in Houston

Share how your transplant experience changed your life?

So far I'm still on the road to recovery but I can breathe better without oxygen

Share whatever information you want us to know about you

I was diagnosed with Cystic Fibrosis before I was born and diagnosed with CFRD by age 14. I was also diangosed with liver disease related to the CF at age 15. I am now 24 years old.

Share your interests and hobbies

Animals, jig saw puzzles, girly stuff

What Part of The World Do you Live? Feel free to share city, state, country

Southeast Texas

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  • Patty, yes it's Google, but everything in this forum is indexed by Google. If you notice, the keywords in the search box above the search results, google searches within transplantfriends only :)

  • Do you see a bar on the top that says "Welcome to our TransplantFriends.com Chat Room" ? There is a Search box on the extreme right of that box :)

  • Oh good...I'm getting to that point too :)
  • Hi.. I didn't know how to reply to your comments till after I sent you a message. Sorry..
  •  Happy Birthday Patty ! 

  • Hi patty
    I LOVE Houston! The drs at Methodist hospital saved my life. Double lung tx last march 3. Also my daughter and her family live in pearland. My 2 year old granddaughter lives there.
    Good luck
  • :) and us you Patty. 

  • Hi Patty

    WOW! Welcome to Transplant Friends. I did not know you had CF until now. Thanks so much for joining us. Let me know if you have any questions after reading how this site works.  Questions help to inspire me to improve this site.

    Take care my new friend

    Hostess Risé


  • Hello Patty, welcome to tx friends. Glad you found us. Enjoy life.

  • Hi Patty, So glad you joined transplant friends. We have quite a few people here who have been diagnosed with Cystic Fibrosis. And others here have multi-transplanted. This is a great site with good people who share and learn from each other and make a friend or two along the way. Please feel free to post, comment and join groups that meet your needs. Wishing you the best.

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