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Acknowledgement: Josh Abbott

point

New member
I don't know this man, and unfortunately he has passed away. I wanted to post it out of respect for him and the work that he and his mother drove to complete. I guess his one statement just stuck with me this morning as I read this article and I wanted others with CF to read it as well as an acknowledgement to Josh.

<i>Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.</i>

Full article below....

Double-lung transplant patient dies at Shands

BY DIANE CHUN

SUN STAFF WRITER
November 10. 2006 6:01AM

Gainesville resident Josh Abbott spent most of his life fighting for every breath. The enemy was cystic fibrosis, an inherited disease that clogged his lungs with sticky mucus and left him vulnerable to repeated bouts of infection and pneumonia.

When Abbott received a double-lung transplant in December, he took a deep breath and began to imagine a future.

He said that every morning when he woke up, he thought about what he could do that day that he wasn't able to do before the transplant.

"And do you know what the answer is?" he said. "Everything!"

However, on Wednesday, he died at Shands at the University of Florida. He was 30.

Those who knew Josh Abbott also know he wouldn't want to be defined by the disease that limited him.

For two years running, he and his mother, Karen Deeter, went before the Florida Legislature, asking legislators to change a loophole in the law that stood between adult cystic fibrosis patients and the lung transplants that could give them a near-normal life.

In the final hours of last year's session, legislators passed a Medicaid reform package that included a clause that made it possible for adult CF patients to gain access to Medicaid dollars that had already been appropriated for lung transplants.

Rep. Larry Cretul, R-Ocala, sponsored the bill in the Florida House, while state Sen. Rod Smith, D-Alachua, pushed a similar measure in the Senate.

Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.

With its passage, the measure made it much less likely that someone would be turned away from a transplant because of an inability to pay.

On Thursday, Cretul said that Abbott had touched him as few of his constituents ever had.

"He was a fighting young man, and everything he did, he did for other people with his condition," Cretul said. "I was blessed to be able to work with him."

Karen Deeter said that her son had attended Saturday services at B'Nai Israel Synagogue, talking with friends, seemingly fine. Sunday afternoon, he collapsed at home.

Funeral services will be held for Abbott at B'nai Israel today at 11.

Abbott had wanted to be an organ donor if anything happened to him, and was able to donate his liver and both kidneys, his mother said.

"He received the gift of life almost a year ago, and, today, he gave the gift of life to others," Deeter said Thursday.

His mother said that Abbott would want those who knew him to remember the good days and the independent breathing he enjoyed for nearly a year.

"As he said so often, 'Every day I wake up is a good day,' "she said.

Diane Chun can be reached at 374-5041 or chund@ gvillesun.com
 

point

New member
I don't know this man, and unfortunately he has passed away. I wanted to post it out of respect for him and the work that he and his mother drove to complete. I guess his one statement just stuck with me this morning as I read this article and I wanted others with CF to read it as well as an acknowledgement to Josh.

<i>Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.</i>

Full article below....

Double-lung transplant patient dies at Shands

BY DIANE CHUN

SUN STAFF WRITER
November 10. 2006 6:01AM

Gainesville resident Josh Abbott spent most of his life fighting for every breath. The enemy was cystic fibrosis, an inherited disease that clogged his lungs with sticky mucus and left him vulnerable to repeated bouts of infection and pneumonia.

When Abbott received a double-lung transplant in December, he took a deep breath and began to imagine a future.

He said that every morning when he woke up, he thought about what he could do that day that he wasn't able to do before the transplant.

"And do you know what the answer is?" he said. "Everything!"

However, on Wednesday, he died at Shands at the University of Florida. He was 30.

Those who knew Josh Abbott also know he wouldn't want to be defined by the disease that limited him.

For two years running, he and his mother, Karen Deeter, went before the Florida Legislature, asking legislators to change a loophole in the law that stood between adult cystic fibrosis patients and the lung transplants that could give them a near-normal life.

In the final hours of last year's session, legislators passed a Medicaid reform package that included a clause that made it possible for adult CF patients to gain access to Medicaid dollars that had already been appropriated for lung transplants.

Rep. Larry Cretul, R-Ocala, sponsored the bill in the Florida House, while state Sen. Rod Smith, D-Alachua, pushed a similar measure in the Senate.

Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.

With its passage, the measure made it much less likely that someone would be turned away from a transplant because of an inability to pay.

On Thursday, Cretul said that Abbott had touched him as few of his constituents ever had.

"He was a fighting young man, and everything he did, he did for other people with his condition," Cretul said. "I was blessed to be able to work with him."

Karen Deeter said that her son had attended Saturday services at B'Nai Israel Synagogue, talking with friends, seemingly fine. Sunday afternoon, he collapsed at home.

Funeral services will be held for Abbott at B'nai Israel today at 11.

Abbott had wanted to be an organ donor if anything happened to him, and was able to donate his liver and both kidneys, his mother said.

"He received the gift of life almost a year ago, and, today, he gave the gift of life to others," Deeter said Thursday.

His mother said that Abbott would want those who knew him to remember the good days and the independent breathing he enjoyed for nearly a year.

"As he said so often, 'Every day I wake up is a good day,' "she said.

Diane Chun can be reached at 374-5041 or chund@ gvillesun.com
 

point

New member
I don't know this man, and unfortunately he has passed away. I wanted to post it out of respect for him and the work that he and his mother drove to complete. I guess his one statement just stuck with me this morning as I read this article and I wanted others with CF to read it as well as an acknowledgement to Josh.

<i>Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.</i>

Full article below....

Double-lung transplant patient dies at Shands

BY DIANE CHUN

SUN STAFF WRITER
November 10. 2006 6:01AM

Gainesville resident Josh Abbott spent most of his life fighting for every breath. The enemy was cystic fibrosis, an inherited disease that clogged his lungs with sticky mucus and left him vulnerable to repeated bouts of infection and pneumonia.

When Abbott received a double-lung transplant in December, he took a deep breath and began to imagine a future.

He said that every morning when he woke up, he thought about what he could do that day that he wasn't able to do before the transplant.

"And do you know what the answer is?" he said. "Everything!"

However, on Wednesday, he died at Shands at the University of Florida. He was 30.

Those who knew Josh Abbott also know he wouldn't want to be defined by the disease that limited him.

For two years running, he and his mother, Karen Deeter, went before the Florida Legislature, asking legislators to change a loophole in the law that stood between adult cystic fibrosis patients and the lung transplants that could give them a near-normal life.

In the final hours of last year's session, legislators passed a Medicaid reform package that included a clause that made it possible for adult CF patients to gain access to Medicaid dollars that had already been appropriated for lung transplants.

Rep. Larry Cretul, R-Ocala, sponsored the bill in the Florida House, while state Sen. Rod Smith, D-Alachua, pushed a similar measure in the Senate.

Abbott, who at that point could not breathe without the aid of a portable oxygen tank, said, "I feel like I'm giving life back to somebody who will need it" when he heard the bill had passed.

With its passage, the measure made it much less likely that someone would be turned away from a transplant because of an inability to pay.

On Thursday, Cretul said that Abbott had touched him as few of his constituents ever had.

"He was a fighting young man, and everything he did, he did for other people with his condition," Cretul said. "I was blessed to be able to work with him."

Karen Deeter said that her son had attended Saturday services at B'Nai Israel Synagogue, talking with friends, seemingly fine. Sunday afternoon, he collapsed at home.

Funeral services will be held for Abbott at B'nai Israel today at 11.

Abbott had wanted to be an organ donor if anything happened to him, and was able to donate his liver and both kidneys, his mother said.

"He received the gift of life almost a year ago, and, today, he gave the gift of life to others," Deeter said Thursday.

His mother said that Abbott would want those who knew him to remember the good days and the independent breathing he enjoyed for nearly a year.

"As he said so often, 'Every day I wake up is a good day,' "she said.

Diane Chun can be reached at 374-5041 or chund@ gvillesun.com
 

HairGirl

New member
Thank You for sharing this, that is so wonderful what he was able to do for those who will need a transplant.
 

HairGirl

New member
Thank You for sharing this, that is so wonderful what he was able to do for those who will need a transplant.
 

HairGirl

New member
Thank You for sharing this, that is so wonderful what he was able to do for those who will need a transplant.
 

Diane

New member
What an inspiring story! Sad, but inspiring. Josh sounds like a very brave and caring man to me.
RIP Josh <img src="i/expressions/rose.gif" border="0">
 

Diane

New member
What an inspiring story! Sad, but inspiring. Josh sounds like a very brave and caring man to me.
RIP Josh <img src="i/expressions/rose.gif" border="0">
 

Diane

New member
What an inspiring story! Sad, but inspiring. Josh sounds like a very brave and caring man to me.
RIP Josh <img src="i/expressions/rose.gif" border="0">
 

coltsfan715

New member
Thank you so much for sharing this article. It brought a slight tear to my eyes because his efforts - in getting that bill passed in Florida has made it possible for friends of mine in the state (I live in FL - about 2 hours from Gainesville) to get a transplant or at least an evaluation within the state. Beforehand my friends had to leave and go outside the state for transplant care because they were denied coverage for transplant and could not be seen due to inability to pay - it is crazy to think that Medicaid would pay for a child (or anyone UNDER the age of 18) to get a lung transplant but anyone over 18 was denied - until this year.

Thank You to him and his mother from a fellow Floridian. My condolences to his family and friends.

Again thank you for sharing,
Lindsey
 

coltsfan715

New member
Thank you so much for sharing this article. It brought a slight tear to my eyes because his efforts - in getting that bill passed in Florida has made it possible for friends of mine in the state (I live in FL - about 2 hours from Gainesville) to get a transplant or at least an evaluation within the state. Beforehand my friends had to leave and go outside the state for transplant care because they were denied coverage for transplant and could not be seen due to inability to pay - it is crazy to think that Medicaid would pay for a child (or anyone UNDER the age of 18) to get a lung transplant but anyone over 18 was denied - until this year.

Thank You to him and his mother from a fellow Floridian. My condolences to his family and friends.

Again thank you for sharing,
Lindsey
 

coltsfan715

New member
Thank you so much for sharing this article. It brought a slight tear to my eyes because his efforts - in getting that bill passed in Florida has made it possible for friends of mine in the state (I live in FL - about 2 hours from Gainesville) to get a transplant or at least an evaluation within the state. Beforehand my friends had to leave and go outside the state for transplant care because they were denied coverage for transplant and could not be seen due to inability to pay - it is crazy to think that Medicaid would pay for a child (or anyone UNDER the age of 18) to get a lung transplant but anyone over 18 was denied - until this year.

Thank You to him and his mother from a fellow Floridian. My condolences to his family and friends.

Again thank you for sharing,
Lindsey
 

beleache

New member
Thank you for sharing that story, There are so many stories tha we never here. My gratitude and my condolences to his family and friends.
 

beleache

New member
Thank you for sharing that story, There are so many stories tha we never here. My gratitude and my condolences to his family and friends.
 

beleache

New member
Thank you for sharing that story, There are so many stories tha we never here. My gratitude and my condolences to his family and friends.
 
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