Claude Brady's Page
Profile Information
- What is your city / state and country of residence?
- Arlington, VA
USA
- How are you touched by transplantation?
- I am a Recipient
- If you are a recipient, what type of transplant did you receive?
- Heart
- If you are a recipient, what type of donor did you receive your Gift of Life from?
- Deceased Donor
- If you are a recipient, when did you have your transplant(s)?
- June 1989
- What is your hospital and, or doctor's name, city / state and country?
- Cyclo (Modified)
- What do you do for a living?
- Retired
- About Me: Please use this space to tell the community about yourself and your unique experience with transplantation:
- There has bee three transplants done at John Hopkins, my brother a heart 1985, my heart 1989, a bone marrow transplant for my wife 1999. I am the only one still alive.
- What is your relationship status?
- Single
- My Personal (non-commercial) Website, Page, or Blog URL:
- http://www.transplantawareness.org
Forum
Cancer Risk for Liver Transplant Recipients 1 Reply
Started by Bill Oltman in New to the Cafe? Introduce Yourself to the Community!. Last reply by Nelson Freytes 54 minutes ago.
help help i am techno- challenged !!! 3 Replies
Started by riki in Website Features Support, Feedback & Suggestions. Last reply by Nelson Freytes 2 hours ago.
How long has your transplanted kidney lasted 2 Replies
Started by Diana in General Discussion & Community. Last reply by Brian 7 16 hours ago.
The Gift of Life 1 Reply
Started by Dianne Lovely in General Discussion & Community. Last reply by Jeffrey Isaacs Oct 9.
scars 7 Replies
Started by riki in General Discussion & Community. Last reply by Peach 1 day ago.
I thought l would say hello! I'm the new girl on the block! 18 Replies
Started by Jane Tucker in New to the Cafe? Introduce Yourself to the Community!. Last reply by riki 2 hours ago.
obstructions 1 Reply
Started by Kandee in Kidney / Pancreas Transplants. Last reply by Troy K. Childers Oct 7.
Hi from Madison, WI 3 Replies
Started by Kim Bolinder in New to the Cafe? Introduce Yourself to the Community!. Last reply by Beth Sharer Oct 8.
Moving on up..... 3 Replies
Started by Meghann M. in Lung Transplants. Last reply by Meghann M. Oct 7.
Solu-medrol 4 Replies
Started by Gail Csizmar in New to the Cafe? Introduce Yourself to the Community!. Last reply by Gail Csizmar 22 hours ago.
Blog Posts
Open Letter To Members of Transplant Cafe.
Posted by Jeffrey Isaacs on October 11th, 2008 at 12:16pm — 5 Comments
Dave Undis And Life Sharers
Posted by Nelson Freytes on October 11th, 2008 at 11:30am — 5 Comments
Bring Mary Jo back!!!
Posted by Suzanne Cicchini on October 9th, 2008 at 8:14am — 4 Comments
HOW DO YOU FEEL ALLOWING INMATES TO DONATE?
Posted by Karen Weddick on October 8th, 2008 at 11:00pm — 9 Comments
He is not a doctor, nor has he been in a "need" situation and wth is this?I am a Transplant Facilita…
Posted by Suzanne Cicchini on October 8th, 2008 at 8:25pm — 7 Comments
LIFE WHAT?
Posted by Suzanne Cicchini on October 8th, 2008 at 8:07pm
Why I joined TransplantCafe
Posted by Gail Csizmar on October 8th, 2008 at 7:33pm
Should Lifeshares be allowed on Transplant Cafe? VOTE NOW!!!!!!!!!!!!!!
Posted by Jeffrey Isaacs on October 8th, 2008 at 5:00pm — 25 Comments
I"m now #1 on the list for my blood type!! :) WOOOOOOOOOOOOO HOOOOOOOOOO!
Posted by Meghann M. on October 5th, 2008 at 3:21pm — 6 Comments
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Comment Wall (10 comments)
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See you soon in St Louis at TRIO/ITNS symposium. Hope you are doing well
Hope you made it back safely. I had a great time in Pitt ... it was very nice meeting you!!
Take care,
Tish :0)
Just FYI, to reply to a comment someone leaves on your page, you must hit "comment back" and leave comment there. Otherwise they don't know you're replying to them. The message you wrote to Jim below, did not prompt him to come read it. You should copy it, hit "comment back" below his message to you, then paste it in the comment box you'll see when you do this.
Take care,
Nelson
Time makes it 60 years since I developed HCM, Dr. then said he didn't know what it was and didn't think there was a doctor in the world that did. Next year will be 50 years since my familys first appointment to NIH, just across the river where we lived. It took NIH three tries (my brother, sister then me) three months of testing to determine the old Dr. was correct.Then after being a patient at NIH for 30 years I received my heart transplant. Now in the process of having DNA testing done to find out which genes are mutated to cause the disease. Have learned many more people have it that I had ever thought.It is the disease that lots of athletics go into ventricle fibrilllation and die on the spot.
I sure wish this site had spell check. I need it. If you google IHSS or HCM there is lots of information there. NIH has always said I am the index patient in the world diagonsed with the disease, That and 59 cents will get me a cup of senior coffee at McDonalds.
I will be in booth 201 at the games, also will be going Monday night on the Quarter Century Club boat ride. Do you have information on the Quarter Century Club?
Claude Brady
Nelson