I’m new to site
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Hi again, Ginni….In addition to our Cathy we also have Scott on the waiting list: http://www.caringbridge.org/visit/scottgallaway
Kim’s husband John, who had a transplant two years ago:
http://www.kimkircher.com
and Josh who, has received a transplant a few weeks ago: http://www.caringbridge.org/visit/jhoneycutt
You are the first on our site scheduled for a transplant list at UCLA. That is fantastic news.
Please, stay in touch.
All my best wishes,
MarionHi Ginnie – Welcome to our family. I wish it were under other circumstances. I am so pleased that you are a transplant candidate. Please keep us posted on your progress. We are here for your family too if they would like to join us. Feel free to ask questions, vent, share, whatever, you need. Blessings, Susan
Hi Ginnie, I am so glad that you are able to get a transplant! I will pray that it happens soon for you. As you will see on this site, members have had good success with transplants. Take care. Nancy
Hi- Ginny I am a CC survivor because of a transplant. I am alive because of Dr. William Chapman at Barnes-Jewish Hospital St. Louis, MO.
I was diagnosed July, 2008 and did the clinical trial involving radiation and chemo. I was transplanted May 24, 2009. I had a second transplant on July 4,2009!! I am a miracle.It will be 21/2 years from diagnosis and I am finally good!! I am alive only because of God and his miracle worker Dr. Chapman. You can read my story at thetelegraph.com under christmas miracle.
I would love to talk to you so feel free to contact me at jrdunnagan@gmail.com. There is HOPE!!!!
Lots of prayers-CathyHi Ginny….if you are the Ginny living in the bay area then I have been following your blog…in fact, if so then we live in close proximity. Ginny, I don’t know whether you have had the opportunity to take a close look at our site because, we have a blog section also where you will find several members who, have undergone liver transplantations. Currently I believe it is Scott going through the process.
Just in case though, whichever Ginny you are I am thrilled that you have found us.
All my best wishes,
MarionHello Ginnie and welcome to our family but sorry you had to find us. Like the boys asked, tell us more about youself. You will find the most caring and loving people here from all over the world. We will be happy to hear more from you!
Hi Ginnie,
Welcome to the site. Sorry that you had to find us all but glad that you have joined in with us as you will get a load of support from everyone here. As Jim has asked, could you tell us a bit more about yourself. And a specific board that may be of interest to you is our transplantation board which can be found here –
http://www.cholangiocarcinoma.org/punbb/viewforum.php?id=46
Please feel free to ask any questions that you have and we will all do what we can to help in answering them. I came here back in 2009 when my dad was diagnosed and it was the best thing that I could have done. Looking forward to reading more of your posts and I wish you every success.
My best wishes to you,
Gavin
Ginnie, sorry you had to find us, and welcome. I think you will find a lot of caring, compassionate and very knowledgeable people here. I didn’t find this site until well after my adventure with CC began, and could have used the support.
Where are you located (we get people from all around the world here) and where are you being treated?
Good luck with your treatment and I hope for a good outcome for you.
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