Tuesday, December 21, 2010

Tracy Morgan Undergoes Successful Kidney Transplant


TODAY news services: Actor and comedian Tracy Morgan is recovering from a kidney transplant undergone earlier this month, his publicist said in a statement on Monday.

Morgan, 42, will miss at least two episodes of the television show, "30 Rock", in which he co-stars with Tina Fey and Alec Baldwin and plays a caricature of his own days on "Saturday Night Live." According to E! Online, his character's absence will be explained by some "happy news."

His successful transplant occurred around Dec. 10.

"Tracy is doing well and taking some much needed time to recover after the surgery," said the statement. "He is looking forward to going back to work after the holidays."

Morgan was diagnosed with diabetes nearly 15 years ago, but said in his first "30 Rock" season he did not take the disease seriously. The episodes Morgan will miss are due to air in March.

As E! Online pointed out, Morgan is the second member of "30 Rock" to have a transplant this year. Grizz Chapman, who was suffering from end-stage renal disease, also received a new kidney.

Reuters and E! Online contributed to this report.

Friday, December 17, 2010

Successful Event Raises More than $17,000!

NFT patient Kenny Cox is a regular on the Florida music scene. When his friends and community members heard of his need for a kidney transplant, they wanted to help. Volunteers held "Blow Out to Go Out," last month in Kenny's honor.

On November 20, the Rock for Hair and Nails salon donated proceeds from hair and nail appointments while several bands, including the Kapo Kings and Chasing Sparrows, played throughout the area. When the day was over, more than $17,000 had been raised in honor of Kenny!



To see more photos from this event, visit NFT on Facebook.

Tuesday, December 14, 2010

NFT Patients Held More Than 200 Fundraisers in 2010

Congratulations to the countless volunteers who held successful fundraisers in honor of NFT patients in 2010! This year, more than 200 events were held across the country to raise funds in honor of our transplant patients.

Thank you to the volunteers, friends, family members and community supporters who made this possible! If you were involved in an NFT fundraiser, please feel free to send your event details and photos to info@transplants.org. We love to hear about them!

Monday, December 13, 2010

Counting Her Blessings

The following article is from The Courier of Montgomery County.

After 14 years of common law marriage, Esmerelda and Jose Luis Miranda officially tied the knot, walking the aisle as friends and family smiled through tears at the La Torretta Lake Resort & Spa Sunday.

Recently as seven months ago, however, this scene would have seemed impossible to the bride.

“This is very, very special. A dream come true for us,” said Miranda, who resides in the Houston area. “I never thought this was gonna happen.”

More than 109,000 people are currently awaiting an organ transplant in the United States, according to LifeGift, a non-profit organization that recovers organs for people needing transplants. Less than a year ago, Miranda was one of them, awaiting a heart at the St. Luke’s Episcopal Hospital in Houston.

Born with a heart murmur, doctors have told Miranda that she would be able to live with the irregular heartbeat. However, she had gone through three open heart surgeries before collapsing in the street in her hometown of Weslaco in 2009 with a hole in her heart “the size of a silver dollar,” said Elvia Valdez, public relations coordinator for LifeGift.

On May 18, Miranda received a transplant after almost a year on the waiting list at St. Luke’s, which she referred as “one of many blessings” she’s experienced recently. The second blessing came from the Wish Upon a Wedding organization, which granted her a dream wedding at the resort, free of charge.

Heather Sims, president of the Houston chapter of the organization, said it was founded in January, and this is the first wedding put on by the Houston branch. Sims spoke with Miranda initially at a presentation at the St. Luke’s hospital several months ago, and Miranda’s story set her apart.

“It was the journey they had gone through to get to where they are,” Sims said.

The organization partnered with Wish Centers to provide the dress, rings, food and location for the wedding. Sims said “a lot of people came together to pull this off” and praised La Torretta for their help, “going above and beyond.”

“It’s a dream come true for all of us,” said husband Jose Luis Miranda. “We’re really appreciative for what they’ve done for us.”

Miranda said the wedding was especially important for her maid of honor, her 14-year-old daughter Josephine Marie Miranda.

“She’s so proud of her father,” Miranda said. “She told me she’s proud of how he’s stood by me through this. She has friends whose parents split up over less.”

Although family were in attendance, several invited guests were friends she has met through St. Luke’s Hospital. Linda Roberts, LVN, and Melissa Roberts, PCA, attended the wedding and said they have grown close to Miranda during her stay at the hospital, as they witnessed her highs and lows.

“We were there to see her when she had given up, so to see her at the wedding is amazing,” Carroll said. “You know you’ve come this close (to patients) when you go to their weddings.”

Randy Creech, of Kingwood, met Miranda through the hospital’s Heart Exchange Volunteer program, of which she also is a member. The group, made up of heart recipients, meets with people awaiting heart transplants and explains the process to them. Creech has seen more than 1,000 possible heart recipients in his 20 years with the program.

He said he was glad to attend the wedding and believes Miranda will continue to feel better with her new heart.

Miranda also volunteers with LifeGift’s Vital Volunteer program, and said her participation is important.

“Because somebody was there for me and explained to me what it’s going to be like,” she said. “I’m just giving back what was given to me.

“I was given a second chance at life. That’s the best gift you can give someone.”

Sofia Perches, outreach coordinator with St. Luke’s, said about 60 heart transplants are done every year at St. Luke’s Cooley Transplant Center and about 2,000 are performed across the country. According to LifeGift, although 10,000 Texans are currently awaiting organs, Texas is last in the country in registered number of donors.

Friday, December 10, 2010

Successful Chicken Barbecue Fundraiser for Transplant Patient

NFT patient Barbara Igney suffers from polycystic kidney disease (PKD), a genetic condition that replaces healthy kidney tissue with cysts, causing the kidneys to stop functioning properly. Doctors say a kidney transplant is her only hope for a second chance at life.

A kidney transplant costs approximately $250,000, and that's only the beginning. Even with health coverage, she faces considerable medical expenses related to her transplant. For the rest of her life, she will need follow-up care and daily anti-rejection medications. The cost of post-transplant medications can range from $2,000 to $5,000 per month--and they are as critical to her survival as the transplant itself.

Volunteers held a chicken barbecue fundraiser in her honor last week to assist with her medical expenses. Even though it was a cold day, they raised more than $1,700!

Tuesday, December 7, 2010

NFT Patient Gets Law License One Year After Near-Death Coma

The following article is from The Daily Citizen in Dalton, GA:

A year ago [...], Nancy Burnett was lying in a coma at Hamilton Medical Center, her life hanging in the balance as her damaged liver continued to poison her body.

Last month, Burnett, a liver transplant recipient, was alert and being sworn in as a member of the Georgia Bar Association as about 20 family members and friends gathered to watch at the Whitfield County Courthouse.

What a difference a year can make.

A member of the bar associations in both Tennessee and New York, Burnett has been a practicing attorney since 1990. In October 2008, however, she was forced to move back in with her family in Dalton after she became extremely ill with non-alcoholic steatohepatitis (NASH), a disease of the liver prevalent in obese individuals.

Years of problems had gone undiagnosed as doctor after doctor failed to understand what caused her legs to leak clear fluid, her mind to become slow and confused and her body to begin shutting down. When Burnett was finally diagnosed, she was shocked, she said. As her condition grew progressively worse, Burnett developed hepatic encephalopathy, a condition that clouds the brain as the body becomes unable to rid itself of the ammonia it produces through normal eating.

Burnett moved in with her brother, Mark, and mother, Pat in Dalton. By then, she could no longer add, subtract or sign her name, let alone practice law.

After Burnett recovered from her coma at Hamilton, she was able to return home only to be hospitalized again at Memorial Hospital in Chattanooga within a week of being released. Burnett said she was sent to Memorial because of her insurance and later went to Piedmont Hospital in Atlanta for tests and eventually for a liver transplant in January.

“I had to lose weight to get the surgery,” she said. “From my heaviest to my thinnest, I’ve lost 150 pounds. I’ve gained some of that back. I’m about a hundred pounds lighter than I was.”

Burnett described liver disease as “a silent killer,” explaining the doctor who diagnosed her estimated she’d had problems for 15 to 20 years. Burnett, who has been listed as an organ donor for most of her adult life, said she did not notice anything was wrong until about 2003 or 2004.

Kathleen Tancrede of Tunnel Hill, one of Burnett’s sisters, said Burnett spent the Thanksgiving, Christmas and New Year’s holidays as well as her birthday last year in the hospital. Burnett turns 48 on Monday and will celebrate by opening her law office at 217 W. Crawford St. where she plans to be a general practitioner.

“I’ll be doing divorce for sure because I did that for 12 years up in New York,” she said. “I’ve done a lot of bankruptcy in New York, so I’ll probably pick that up.”

Burnett was sworn in before Superior Court Judge Jack Partain on Friday along with law interns Robert Mikell and Kevin Morris, both of whom are completing year-long internships in the superior court system. Burnett has volunteered her time as a clerk at the office since July.

Judge Robert Adams said he has observed “a high standard” in Burnett and that she often took care of problems before he was even aware they were there.

Mark Burnett said seeing his sister be sworn in to practice law in Georgia was like watching a family member get a gold medal in the Olympics. In addition to her brother and sister, her mother, Pat, her father Reg and her stepmother Jean as well as several other family members and friends were all present.

Family members said several community members had donated money to her to help her cover her more than $100,000 in medical bills, and local churches had prayed for Burnett to get better. Burnett said she awoke from her coma at Hamilton on a Sunday shortly after morning church services released.

“There were at least three or four local churches praying for me,” she said. “It just really confirmed my belief (in the power of prayer).”

“I’m just so grateful to the community for all the support that they’ve given me and for the (50-year-old female) donor that she elected when she was alive to be a donor when she died,” she said.

Burnett graduated from Dalton High School in 1981 and was the STAR Student that year in recognition of having the highest SAT score at the school, she said. As a reward, she and other STAR students across Georgia received a tour of the state and were able to briefly meet Jimmy Carter.

Burnett graduated from Georgia State University, changing her major a few times as her interests swung between computer programming, international studies and accounting. Finally, her parents suggested she pursue a career in law.

“I fell absolutely in love with the study of law,” she said. “It absolutely captivated me. The study of law is very elegant.”

Burnett attended law school at Georgia State University for her first year then graduated in 1989 from Albany Law School in New York. She practiced in New York for 12 years and since 2003 in Tennessee.

Friday, December 3, 2010

December Patient of the Month: Patrice Martin

In 2009, Patrice was diagnosed with chronic renal failure, which also afflicts her father and aunt. Soon after her diagnosis, she began enduring regular dialysis treatments, which take a toll on her quality of life. Doctors have said a kidney transplant is critical to her survival. Although she has not found a donor match yet, several family members and friends are being tested to see if they could donate a kidney to save Patrice's life.

This devoted mother of two is determined to beat this disease so she can spend many more years with her children. Patrice says her children are her motivation to stay positive on a daily basis. After receiving her transplant, she looks forward to going back to work, taking walks and traveling. Because her illness leaves her so exhausted, her activities are greatly limited. More than anything, Patrice is anxious to have energy and resume her normal activities. But she needs your help.

To learn more about Patrice or to make a donation in her honor, please visit her web bio.

Thursday, December 2, 2010

Myths and Facts about Bone Marrow Donation

Every year, more than 10,000 patients in the U.S. are diagnosed with life-threatening diseases such as leukemia or lymphoma, and their best or only hope of a cure is a transplant from an unrelated donor or cord blood unit. The need for transplants is increasing. Medical advances are making transplants a treatment option for more patients of all ages than ever before.

Below is information from Be the Match to clear up some common myths about bone marrow donation. To learn more about joining the Be the Match bone marrow registry, visit their website.

MYTH: Marrow donation is painful.
FACT: General or regional anesthesia is always used for this procedure. Donors feel no needle injections and no pain during the marrow donation process. Afterward, most donors feel some pain in the lower back for a few days or longer.

MYTH: All marrow donations involve surgery.
FACT: There are two ways to donate. The majority of donations do not involve surgery. The patient’s doctor most commonly requests a peripheral blood stem cell (PBSC) donation, which is non-surgical and outpatient. If the patient’s doctor requests marrow, marrow donation is a surgical procedure, usually outpatient.

MYTH: Pieces of bone are removed from the donor.
FACT: Pieces of bone are not removed from the donor. In marrow donation, only the liquid marrow found inside the bones is collected. In a PBSC donation, cells are collected from the bloodstream in a process similar to donating plasma.

MYTH: Donating marrow is dangerous and weakens the donor.
FACT: Though no medical procedure is without risk, there are rarely any long-term effects from donating. Only five percent or less of a donor’s marrow is needed to save a life. After donation, the body replaces the donated marrow within four to six weeks. The National Marrow Donor Program (NMDP), which operates the Be The Match Registry, screens all donors carefully before they donate to ensure they are healthy and the procedure is safe for them. The NMDP also educates donors, answers questions every step of the way, and follows up with donors after donation.

MYTH: Marrow donation involves a lengthy recovery process.
FACT: PBSC donors take the drug filgrastim for five days leading up to donation and may have symptoms such as headache, bone or muscle pain, nausea, insomnia or fatigue during this time. These symptoms nearly always disappear one or two days after donating, and the donor is back to normal. Marrow donors can expect to feel fatigue, some soreness or pressure in their lower back and perhaps some discomfort walking. Marrow donors can expect to be back to work, school and other activities within one to seven days. The average time for all symptoms to disappear is 21 days.

MYTH: Donors have to pay for the donation procedure.
FACT: Donors never pay for donating and are never paid to donate. All medical costs are paid by the patient’s medical insurance or by the patient, sometimes with assistance from the National Marrow Donor Program (NMDP). The NMDP, which operates the Be The Match Registry, reimburses donors for travel costs, and may reimburse other costs on a case-by-case basis. Although a donor never pays to donate, many people do pay the tissue-typing cost when they join the registry.

Monday, November 29, 2010

NFT Christmas Angel

Transplant patients are dealing with very difficult physical, emotional and financial situations. As you might imagine, the financial burdens associated with transplantation often make celebrating the holidays impossible for families. For the past three years, generous families and groups have reached out to NFT asking if they could play Santa for a transplant patient and their family.

In 2008, NFT patient Wess Holston and his family were overwhelmed by the generosity of an anonymous donor family.

“May God bless the Denver family,” said Katrina, Wess’ wife. “There will be tears of joy this Christmas, not tears of guilt. There are no words to describe how much this means to us, and we thank this family and NFT for their help. Our children are going to have a great Christmas this year.”

If you would like to surprise an NFT patient by supporting them during the holiday season, please contact us at info@transplants.org.

Wednesday, November 17, 2010

A Country Wedding Fundraiser

NFT patient Karen Ettinger needs a double-lung transplant to survive. Her twin brother, Kevin, wanted a way to help her raise funds for the lifesaving treatment. He owns a collection of antique wedding dresses and invited people to his home to see the collection, while raising funds in honor of NFT.

They raised nearly $6,000, and the event was such a huge success that they may hold a second one in the spring! A portion of the funds raised came from a raffle in which lucky winners received items such as a christening gown and a gift certificate from designer Alfred Angelo.













Thursday, November 11, 2010

National Donor Sabbath

This weekend, November 12--14, is recognized as the National Donor Sabbath.

National Donor Sabbath is part of an organ donation initiative launched by the Department of Health and Human Services in 1997. Observed on Friday through Sunday two weekends before Thanksgiving, the 3-day period seeks to include the days of worship of major religions practiced in the U.S.

Transplant professionals collaborate with faith communities to focus on the lifesaving gifts of organ, tissue and marrow donation. Faith leaders and congregations participate in services and events to increase awareness of donation and transplantation. Most major religions view organ and tissue donation as a compassionate and generous gift.

The need for donors increases each year. Currently, nearly 110,000 Americans are on the organ transplant waiting list. According to OrganDonor.gov, an average of 3,000 individuals at any given time are searching for an unrelated blood stem cell donor.

Those who donate organs, tissue, and blood stem cells restore hope and share gifts beyond measure. For more information about becoming an organ donor, visit the NFT website. Together, we can continue raising hope and changing lives.

Tuesday, November 9, 2010

Miracle Minute in Honor of Kevin Bolin

Volunteers for Kevin Bolin held a "miracle minute" fundraiser at a local high school football game last month.

Kevin's two brothers and sister went on the track after the first quarter of the football game, and the announcer read a speech while they held Kevin's picture. Volunteers passed buckets through the stands and raised more than $2,000!



Kevin's mother, brother and sister.


Kevin's sister and brother.

Monday, November 8, 2010

Miami Transplant Institute Celebrates 40th Year

The following article is from Miami's CBS4.com.

This year the Miami Transplant Institute at the University of Miami/Jackson Memorial Medical Center is celebrating four decades of lifesaving organ and tissue transplants.

The program, regularly recognized for its excellence in clinical care and high success rates, was honored in 2010 for three of its transplantation programs which received national recognition for extraordinary performance from the U.S. Department of Health and Human Services.

On Monday, several people who had life saving transplant operations from MTI gathered at the hospital to join in the celebrations for 40 years of success.

Andrea Kessler, the program's first kidney-pancreas transplant patient, has had her organs for 20 years.

"My life was different. I feel like a very new person having had these transplants," said Kessler, "Made me stronger and made my family stronger."

Kessler, a practicing attorney working in several legal areas including probate, trust, litigation and medical devices said the whole purpose of going through the transplant process was to get back her life.

"All of the recipients are part of our family, but those with the complications become the closest part because we have to live with them," said UM/Jackson surgeon Dr. George Burke.

"I've done great with the transplant," said Mark Frye, "And everything is fine."

Dr. Kathryn Smith, now a resident at UM/Jackson, said her first trip to the hospital was 11 years ago as a patient in need of a transplant. Smith underwent a multivisceral transplant in 1999 and is one of the longest living survivors of this rare procedure.

"I sort of always wanted to be a doctor, but actually this experience did, I guess, strengthen my desire to be a physician."

Former UM football player Ron Walker, 54, had a heart transplant at UM/Jackson this past May and said it has changed his life.

"I can't thank you enough because without you all, I wouldn't be here today. I thank God for all of you. These people here (gesturing at the doctors) are now my new heroes. It was Michael Jordan and LeBron James, nothing against them guys, but when something happens to them, who are they going to turn to," said Walker, "These people here."

More than half of all the reported multi-organ transplants in the world have been performed at the institute. One of the reasons for this is that MTI at UM/Jackson is the only Florida hospital to perform every type of organ transplant; more than 500 organ and tissue transplants each year.

Friday, November 5, 2010

The Journey of a Double-Lung Transplant Recipient

When he was just 2 years old, Cody was diagnosed with cystic fibrosis, a lung disease that affects about 30,000 people in the United States. Though he was able to live a relatively normal life and was only hospitalized once because of his illness, his health began to worsen in 2009. Last year Cody spent almost 3 months in and out of the hospital, including several stays in the ICU.

Click here to watch a short video of Cody's transplant journey.

Thursday, November 4, 2010

November Patient of the Month: Jonathan Amarillo

When Jonathan's mother, Yuberky, was pregnant, she won a 4D ultrasound in a contest. During that ultrasound, she learned her little boy was suffering from polycystic kidney disease (PKD). Doctors said Jonathan wouldn't survive because his kidneys were so enlarged that his lungs couldn't develop properly. Jonathan has had both kidneys removed and requires dialysis treatments at home for more than 10 hours each day. Doctors have said a kidney transplant is critical to his survival.

Rather than arranging play dates and playing silly games with her baby boy, single mom Yuberky must spend her time scheduling doctors' visits and dialysis treatments for little Jonathan. They are facing a difficult challenge, but Yuberky is determined to be there for her son and see him overcome this health battle.

A kidney transplant costs approximately $250,000. And that's only the beginning. Even with insurance, Jonathan's family faces significant medical expenses related to his transplant.

To read more of little Jonathan's story or to make a donation to NFT in his honor, please visit his web bio.

Tuesday, November 2, 2010

NFT Patients Who Received Transplants in October

We are thrilled for the NFT patients who received their transplants last month, and we wish them all the best during recovery!

As you may already know, NFT provides services to transplant candidates awaiting organ and/or tissue transplants, as well as patients who have already received their transplants.
To learn more about NFT and our transplant fundraising services, visit the FAQ page on our website.

Friday, October 29, 2010

A Bluegrass Emergency

The following article is from the Cary Citizen.

After recovering from having a heart pump implanted this past spring, musician Jan Johansson was added back onto the heart transplant waiting list in July. His friends have organized a fundraiser to help him and his wife, Theresa, defray his medical expenses. PineCone helped with a benefit held at Sertoma Amphitheatre this past June. That event raised about $4,000.

On November 7 there will be another benefit concert to raise funds for the Johanssons at Cary’s Sertoma Amphitheater.

Among the musicians and bands confirmed for this latest benefit concert is David Tate, a banjo player who is also Johansson’s cardiologist at UNC-Chapel Hill. Tate plays with the band Fescue 911, which has been “on-call for bluegrass emergencies” since 1993.

And what could be a more fitting emergency than a bluegrass musician in need of a heart transplant?

To read the full article, click here.

Friday, October 22, 2010

Man To Run NYC Marathon After Double-Lung Transplant

From CBSNewYork.com:

A Connecticut man is running his first marathon next month. That might not sound unusual except for the fact that last fall he couldn’t walk across a room.

One year ago, Tim Sweeney could barely walk without wearing an oxygen mask. One year ago, both Tim and his wife, Beth, believed his days were numbered, reports CBS 2′s Dana Tyler.

“I always knew there was something different when I grew up. I always had a slight cough in the morning, but as the day went on, it became less and less,” Tim said.

For years, he had no idea that he’d been diagnosed with cystic fibrosis when he was 2 years old. Cystic fibrosis is a genetic disorder in which the body produces a thick mucous that clogs the lungs and hampers digestion.

Tim never missed a day of school, though. His mother gave him the proper medications; his father pushed him to be athletic. They didn’t label him.

“He was so young. We didn’t want to stop him from doing anything, to be as normal as possible, to play with his brothers and do what everybody else did, so we didn’t tell him when he was young,” Tim’s mother, Rose Sweeney, said.

Tim was always athletic. He finished college and worked as a fitness trainer. When he and Beth started dating, she heard something in his chest, and insisted he see a doctor.

“They asked, ‘how long have you known you had cystic fibrosis,’ and I was 26, 27, and I was like, ‘whoa,’” Tim said. “To me, it was a bombshell. Now, all of a sudden, it was real. I looked it up, life expectancy was 37 or something. It was a major shock.”

That was in 2004. Tim said he felt fine and always thought he could beat it, but in 2007 – soon after the couple married – his health began to decline.

They were able to have a baby through in vitro fertilization, but doctors told the new father he had 18 months to live if he didn’t undergo a lung transplant.

Tim recalled the agonizing wait for a donor.

“There’s someone out there leading a normal life. Typically it’s an accident victim, so it’s sudden,” Tim said. “It’s such a tragic and beautiful thing all at once. You know it’s going to happen.”

When his normal treatments failed last fall, Tim was unable to breathe on his own. With double pneumonia, Sweeney was quickly moved to the top of the list for a rare double lung transplant.

“I was 120 pounds, I was so weak, eyes sunken in, losing hair,” Tim said.

After three false alarms, Dr. Joshua Sonnett transplanted the lungs of a 25-year-old accident victim last Nov. 10, saving Tim Sweeney’s life.

“Medically, he was at a point, he was around 20 percent of where he should be. He lost 80 percent of his lung function,” Dr. Sonnett said. “Once you get in the 20 percent range, basically in a window, if he got an infection he could have died.”

Only 100 double lung transplants are performed in the United States each year. Tim woke up in intensive care wondering how the transplant went, when Dr. Sonnett shocked him with a question.

“He said, ‘I understand you’re a trainer. I just did the NYC marathon,’ and I thought that would have been great, especially with new lungs,” Tim said. “He said, ‘Why don’t we do that?’”

“He said, ‘I’ll run it with you next year.’ I didn’t expect him to do it,” Dr. Sonnett said. “[But] I knew he could, I knew he could.”

Dr. Sonnett said Tim’s lifelong commitment to a good diet and exercise – even walking the hospital corridors with weights – ensured his speedy recovery. He was released from the hospital in a week, and there’s still been no infection and no rejection.

“He woke up every night, for every night for two years, having coughing fits,” Beth said. “[Now] there was no coughing, no heavy breathing, no oxygen sound. I’m lying there, dead silent – we just started laughing.”

And now, there’s no stopping him. Beth designed T-shirts to raise money for medical costs and cystic fibrosis, and be his coach.

“I try to get him to lengthen his stride and lean forward a bit,” Beth said. “I run behind him on these things so he doesn’t get an injury that day.”

The little boy with the cough now has wings on his heels, and he doesn’t run alone. He’s grateful to his doctors, the donor and his family.

“It felt like something…I was doing something I was born to do,” Tim said. “This is what came natural to me, to go outside and go running.”

Tim Sweeney’s first marathon will be on Nov. 7, and even though it’s Dr. Sonnett’s fourth, he said it’ll be tough keeping up with Tim and his new lungs.

Tim and Beth hope his story inspires others waiting for organ transplants – that they know that yes, it’s a long and often dire road, but there are heroes all around us sharing the gift of life.


Thursday, October 21, 2010

Groundbreaking Stem Cell Transplant Surgery Done at Emory

From Fox5 Atlanta:

ATLANTA, Ga. - A groundbreaking surgery took place Wednesday, Oct. 20 at Emory University Hospital as a 58-year-old Hoschton man, who was diagnosed with the neuro-degenerative disease ALS, had a stem cell transplant.

John Conley is only the seventh ALS patient in the country, and the first who is still able to walk. To undergo the high-risk experimental surgery, Conley says he was a bit nervous, but he was ready for the very delicate operation.

Neurosurgeons at Emory actually opened up Conley’s spinal cord, and then they delivered five injections—each containing 50,000 fetal stem cells along the bottom of his spinal cord.

The procedure has never been done before, so no one knows if it’s safe. But, Conley and his wife, Sandy, say he volunteered for the trial knowing there are no guarantees.

Conley’s surgery wrapped up on Wednesday afternoon.

FOX 5’s Beth Galvin was in the operating room during the groundbreaking surgery. She’ll have an update on Conley’s progress on the FOX 5 News at 5 on Monday, October 25.


Tuesday, October 19, 2010

Bingo Fundraiser a Big Hit!

Volunteers for NFT patient Richard Calm held a successful bingo fundraiser last month. For $20, attendees played bingo and had a hot dog lunch with chips and a drink! Gift baskets were also given away in a raffle, and baked goods were available for a donation. The event raised nearly $2,000 in honor of Richard!

If you'd like to plan a bingo fundraiser for your campaign but need a few ideas or tips, feel free to contact us at info@transplants.org.

Richard's grandson Thomas with his great-grandmother.


The gift basket table.



Friday, October 8, 2010

October Patient of the Month: Vicki Lauer

In 2004, Vicki was in an accident that caused an inhalation injury. She awoke in the ICU after being in a coma for two days, and she was diagnosed with end-stage lung disease. Her disease has worsened over the years, and doctors say a double-lung transplant is essential to her survival. While she awaits her lifesaving transplant, she depends on an oxygen tank 24 hours a day.

Her illness has caused many challenges for Vicki, emotionally, physically and personally. However, she is grateful for the lessons she has learned, and she looks forward to receiving a second chance at life. Vicki says if she is blessed with her transplant, she will spend more time paying attention to the truly important things in life and encourage others to do the same.

A double-lung transplant costs approximately $650,000. And that's only the beginning. Before the hospital will add her to the transplant waiting list, she must raise $40,000.

Although she loves her work as a clothing designer, she is currently unable to work because cutting and draping the fabrics is too physically taxing, adding to her financial strain. Because she lives more than 175 miles from the transplant center in New Orleans, she must temporarily relocate to be near the hospital during recovery, incurring significant expenses for travel, food and lodging.

To learn more or to donate to NFT to assist Vicki with her transplant-related expenses, visit her web bio of the NFT website.

Wednesday, October 6, 2010

Florida Musician Awaits Kidney Transplant

NFT patient Kenny Cox needs a lifesaving kidney transplant. His son will donate one of his kidneys to save his father's life. Below is a video Kenny's fundraising volunteers have created on his behalf, featuring a song written and performed by Kenny.


Tuesday, October 5, 2010

Let NFT Tell Your Story!

Are you an NFT transplant patient whose friend has been by your side throughout every health challenge you've faced? Has a friend offered to be your donor match or done something else incredibly generous for you?

A national health magazine is looking for powerful stories about friendships, and NFT's marketing department would love to hear from YOU. The deadline for us to pitch the story is Tuesday, October 6 at 7 p.m. EST, so act quickly!

If you have a story we can share on your behalf, please contact us at info@transplants.org.

Living Kidney Donation Webinar

KidneyLink is hosting “Learning About Living Kidney Donation,” a webinar hosted by Harvey Mysel of the Living Kidney Donors Network on Tuesday, October 12 at 8 p.m. (ET). The webinar will teach people how to raise awareness about living kidney donation and how to tell others about their need for a kidney transplant.

Medical professionals say the only way to increase kidney transplants is to increase the number of kidneys available. Living kidney donation is a key way to help this occur. Many people, however, don’t know a lot about living kidney donations or are afraid to ask someone for a kidney.

To learn more about the upcoming webinar or to register to attend, visit the KidneyLink website.

Monday, October 4, 2010

Paired Kidney Exchange Links Donors and Recipients

The following article is from the Reporter, Vanderbilt University Medical Center's weekly newspaper.

Amy Ragsdale and Brenda Copeland have a lot in common.

Both suffered from polycystic kidney disease, an inherited kidney disorder. Both relied on dialysis for survival, needed kidney transplants and had several folks willing to donate. But neither of them had a compatible match among their donor pool.

Luckily the pair had another thing in common--Vanderbilt University Medical Center.

Coordinators with the Vanderbilt Transplant Center recognized that both patients had exactly what the other patient needed--donors that were blood-type compatible.

Ragsdale, who is B positive, had a pool of potential donors that had A-blood typing while Copeland's donor pool was populated with B-blood types. She needed A's.

“Thankfully, Vanderbilt noticed that there was another family on the waiting list who had the exact opposite scenario as me,” said Ragsdale. “They ran a cross-match and found that we were compatible with the other's donor. We are just so fortunate to have such incredible donors.”

On Sept. 16, both women were successfully transplanted, through a paired kidney exchange.

Murfreesboro resident Ragsdale, 29, had hoped to receive a kidney from her sister-in-law Courtney Mobley, while Alabama resident Copeland, 64, was to receive longtime friend Terry Green's kidney.

But instead, donors and recipients were swapped. And in the end, everyone accomplished what they set out to do.

“This was the easiest type of swap,” said David Shaffer, M.D., professor of Surgery. “Logistically, it is easier if we can find a swap within our own center. That way patients don't have to travel, nor do we have to ship organs to another center. Everyone is in one place.

“Although swaps are challenging, they are a way to increase living donor transplants,” said Shaffer, surgical director of the kidney/pancreas transplant program. “We will be able to improve patient outcomes and reduce the need for patients to be placed on long waiting lists for a deceased donor transplant. This gives patients the best possible kidney in the shortest possible time.”

This is Copeland's second transplant. First diagnosed with kidney disease at age 27, she received her first kidney in 2005. She has been on dialysis for two months awaiting another transplant.

“Anyone who has been on dialysis knows your quality of life is not good,” said Copeland. “It's just a way to exist. This transplant, although not a cure for my disease, will give me my life back.

“I've been so sick that I spend most of my time in the house. I am so looking forward to getting out more. This is a perfect time to start a walking program, don't you think?”

Ragsdale, who had both kidneys removed over the summer, has lived with polycystic kidney disease since she was 12. She said she can barely remember what feeling healthy is like.

“It has been such a struggle and battle for me,” said Ragsdale. “There are just so many things I am looking forward to. The doctor said I will feel better than I have felt since I was a teenager. For the rest of my foreseeable future I will have a sense of normalcy.”

Donor coordinator for living donor transplants, Verna Johnson, R.N., is pleased the transplants went well.

“There are so many obstacles that can arise when finding compatible organs,” said Johnson. “It's not as simple as finding matching blood types. There's a lot more testing that goes on. But it really all comes down to patience and time to find those perfect donors.”

All patients were discharged and will continue to be followed on an outpatient basis.

Monday, September 27, 2010

NFT Patient Has Successful Spaghetti Luncheon Fundraiser!

Ross Gathings is awaiting a kidney/pancreas transplant. When Ross was 9 months old, he was diagnosed with diabetes, which he has been fighting his entire life. In 2002, he began to lose kidney function, and by 2009 his kidneys had completely failed. Most recently, Ross was diagnosed with end-stage renal failure and pancreas failure.

Volunteers recently held a spaghetti luncheon in Ross' honor to help offset the costs of his medical expenses. The event was a huge success and raised more than $2,700!





Friday, September 24, 2010

Let NFT Help With Your Media Outreach!

Did you know NFT's marketing department is ready to help you promote your events by reaching out to your local media? If you are planning an event, be sure to contact your fundraising consultant and ask for our fundraising event form to provide us with the details we need to create a press release.
  1. NFT has access to an extensive database of media outlets across the country. We can create a distribution to quickly and easily reach your local media.
  2. Many newspapers and TV stations have specific guidelines for how press releases should be written and submitted, and some will discard a press release if it's written incorrectly. NFT's marketing department follows those guidelines with every press release to increase the likelihood of media coverage. Many papers will print our releases word for word.
  3. Receiving a press release or media request from NFT provides credibility to the story and fundraising campaign.

First Intestine Transplant Performed In Michigan

DETROIT – The first intestine (bowel) transplant in Michigan was performed on a 50-year-old patient from Port Austin by physicians at Henry Ford Hospital.

The 11-hour surgery was performed on August 21 and 22. The composite multivisceral transplant procedure included transplant of the patient’s small bowel, stomach and pancreas.

Only a few centers in the United States offer intestine transplants and Henry Ford is the only one in Michigan with a program.

The patient, Brent Patterson, who suffered from short bowel syndrome as well as insulin-dependent diabetes, had been waiting for a transplant since April.

Patterson previously had six bowel procedures in a year to treat his intestines, damaged from Crohn’s disease and poor blood supply, and was no longer able to absorb the nutrients his body needed.

“I got so tired, my immune system was low and I would have to eat nonstop just to get enough nutrients,” says Patterson.

To read the full press release, visit the Henry Ford Hospital website.

To watch a video interview with transplant recipient Brent Patterson, visit ClickOnDetroit.com.

Wednesday, September 22, 2010

Jewish Community Hero of the Year Award

After Jay Feinberg waited four years to find a bone marrow donor match, he made it his life's work to save other people by increasing the representation of Jewish people in the world-wide registry. Today, Gift of Life Bone Marrow Foundation is among the top international registries, with more than 170,000 potential volunteer donors, and is responsible for the facilitation of more than 2,100 bone marrow transplants worldwide.

Jay's vision is simple: A match. Anytime. Anywhere. For anyone.

To read more about Jay and to vote for him as the Jewish Community Hero of the Year, click here.

Wednesday, September 8, 2010

September Patient of the Month: David Fraser

Around Easter of 2009, David Fraser and his family had just arrived at the beach for vacation when he had a seizure while unpacking the car. He was rushed to the hospital, and was soon transported to a larger hospital in Orlando, where he stayed for nearly a week. For the next few months, numerous tests and procedures were done until doctors discovered David was suffering from liver disease. Doctors told him a liver transplant was essential to his survival. Thankfully, he received his lifesaving transplant earlier this month and is recovering well.

This hardworking man has a positive attitude and sees no point in focusing on the negative things in life. Even throughout multiple hospitalizations, he has remained optimistic. His personal motto is, "What possible benefit can I get from having a bad or sour attitude?"

David and his wife, Vickie, have three children who hate seeing their dad so sick. His young son still says, "Daddy, don't pick up the black suitcase!" because that is the last memory he has before seeing his dad suffer from a seizure. David loves to spend time outdoors, golf, attend sporting events and play with his children, but his health has prevented him from enjoying his favorite activities very often. Before becoming ill, he spent countless hours volunteering for local charities and planning fundraisers for organizations such as the American Red Cross and Huntington's Disease Society of America. Now, he simply looks forward to resuming a normal life without feeling exhausted all the time.

A liver transplant costs approximately $500,000. And that's only the beginning. Even with health insurance, David faces significant medical expenses related to his transplant. For the rest of his life, he will need follow-up care and daily anti-rejection medications. The cost of post-transplant medications can range from $2,000 to $5,000 per month--and they are as critical to his survival as the transplant itself.

To read more about David or to make a donation to NFT in his honor, visit his web bio.

Tuesday, September 7, 2010

A Patient's Mission: Recruit Marrow Donors

The following article is from the August 23, 2010 edition of People magazine.


Anh Reiss was headed to the gym in February 2009 when she got the call that changed her life. Test results held unimaginable news: She had a rare blood disorder and perhaps only six months to live. Her only hope, her doctor told her, was a bone marrow transplant that could restore her ravaged immune system. But Reiss learned to her dismay that she had a far slimmer chance than many Americans of finding a suitable donor.


Although there are more than 8 million potential donors on the national Be the Match Registry, Reiss' search yielded only 15,000 of Vietnamese descent--whose genetic makeup was most similar to her own--and none was a match. The mother of two despaired. "The thought of leaving my family was overwhelming," says Reiss, who is herself an ob-gyn. "I cried a lot."


But rather than give up, Reiss took action. She and husband Josh, 42, a lawyer, began crisscrossing the Midwest and showing up at Vietnamese festivals to break down cultural barriers against becoming a donor. Allaying fears, sharing her story and swabbing cheeks herself, she has helped add as many as 10,000 Vietnamese donors to the registry. "There's no telling how many lives she's saved," says Mary Halet, director of recruitment for Be the Match.


Reiss--who came to this country at age 7 as part of the wave of Vietnamese "boat people" in the 1970s--noticed she was feeling weak on a vacation last year. The lifelong runner was shocked to learn she had myelodysplastic syndrome (MDS), a life-threatening disorder that usually strikes older people. "I've never smoked, I eat right. There's a 'Why me?' component in this." More grim news: None of her five siblings was a match; she'll need an unrelated donor.


Rather than dwelling on her bad luck, Reiss is thrilled she may have been able to help people like Matthew Nguyen, 28, a pharmacy student from San Francisco diagnosed with leukemia in 2007. On dialysis, he finally found a match in early 2009, shortly after one of Reiss' drives, and is in remission. "I owe Anh gratitude," he says, "that I can never repay."


Although Reiss has yet to find her own lifesaving match, she controls her condition through medication--she's back to practicing medicine full time and works out four days a week--and treasures every moment with Josh and children Alexandra, 19, and Aaron, 15. "No one is guaranteed more time, "she says. "Whatever time I have, I'm going to make the most of it."


By: Steve Helling in Houston and Jennifer Wren in New York.

NFT Patients Who Received Transplants in August

We are so happy for our patients who received lifesaving transplants last month! We wish them the very best in their recoveries.


Wednesday, September 1, 2010

Willie Kemp on WREG's "Pass It On"

This week, Willie Kemp, whose mother needs a lifesaving kidney transplant, was featured on WREG's Pass It On segment. A dedicated University of Memphis supporter chose to track Willie down to let him know that Tiger nation is supporting him through this difficult time.

Wednesday, August 25, 2010

Memphis Area Yard Sale

Volunteers for NFT patient and liver transplant recipient Kelly Bradley are holding a yard sale in her honor. This event is a part of Bartlett’s citywide yard sale. If you would like to donate items for volunteers to sell at the yard sale, please contact info@transplants.org.


Yard Sale in Honor of Kelly Bradley


September 11, 2010


7 a.m. to 1 p.m.


Singleton Community Center


7266 Third Road in Bartlett, TN


In 2008, Kelly was diagnosed with a life-threatening liver disease, after years of battling a platelet problem. Many days, this disease left her feeling exhausted, dizzy and disoriented, and it often caused bleeding from her nose and mouth.

Doctors told Kelly a liver transplant was her only hope for survival. Fortunately, she received her lifesaving transplant in January and is recovering well. She looks forward to the day when she can be independent and not have to worry about her health or finances. Despite her struggles, Kelly feels blessed and is thankful to be alive.

If you’d like to get involved with an NFT patient’s fundraising campaign, please e-mail info@transplants.org, and we will connect you with the appropriate fundraising consultant.

Wednesday, August 11, 2010

NFT Hires Spanish-Speaking Fundraising Consultant

We're thrilled to announce a new addition to our NFT family! In January, Claire Prince joined our staff as a fundraising consultant. Claire works primarily with patients in the northeast region of the country. A professional fundraiser and active member of the Association for Fundraising Professionals, Claire is also a licensed clinical social worker. She's a perfect fit to help patients during their transplant journey.

In the past several years, we've received many requests from Spanish-speaking patients, but we didn't have a staff member to communicate with them in their own language. We realized this need was great and began our search for a consultant with this specialized skill. Claire is fluent in the language and has extensive experience working with the Latino community in her previous jobs. She also served in the Peace Corps in Costa Rica for two years, immersing herself in the culture.

Wednesday, August 4, 2010

August Patient of the Month: Cody Sheets

When he was just 2 years old, Cody was diagnosed with cystic fibrosis, a lung disease that affects about 30,000 people in the United States. Though he was able to live a relatively normal life and was only hospitalized once because of his illness, his health began to worsen in 2009. Last year Cody spent almost 3 months in and out of the hospital, including several stays in the ICU.

Doctors told Cody a double-lung transplant was critical to his survival. Thankfully, he received his lifesaving transplant August 4 and is doing well. We wish him the very best in his recovery!

A double-lung transplant costs approximately $650,000. And that's only the beginning. Cody faces significant medical expenses related to his transplant. For the rest of his life, he will need follow-up care and daily anti-rejection medications. The cost of post-transplant medications can range from $2,000 to $5,000 per month--and they are as critical to his survival as the transplant itself.

Cody's hometown of Yukon, OK has dedicated Saturday, August 28 to Cody as they have multiple events planned throughout the city in his honor. Events include a car show, pancake breakfast, motorcycle run, golf tournament and run/walk.


If you live in the Oklahoma City area and would like to be involved at any of these events, e-mail us at info@transplants.org so we can connect you with the appropriate volunteer in Cody's campaign. If you would like to make a donation to NFT in honor of Cody, visit his web bio on the NFT site.

Tuesday, July 27, 2010

National Minority Donor Awareness Day

Sunday, August 1 is National Minority Donor Awareness Day. This day is observed every August 1 to increase awareness of organ donation among African American, Hispanic/Latino, Asian, Alaskan Native, Pacific Islander and Native American populations.

Currently, 108,000 Americans waiting for organ transplants. Nearly 60,000 of those waiting are minorities.

Unfortunately, there is a drastic shortage of minority organ donors. In fact, last year only 2,055 organ donors were African American, and only 2,031 donors were Hispanic.

Are you an organ donor? If you'd like to learn more about organ donation and how to register as a donor, visit the Transplant Challenge section of our website. If you are interested in being tested to be a living donor for someone, contact the patient's transplant center to begin the evaluation process.

Friday, July 23, 2010

Applebee's Flapjack Fundraiser

Volunteers held a Flapjack Fundraiser at Applebee's in Shelby, NC in honor of NFT patient Kevin Randall! The event was a huge success and raised approximately $1,300!

Did you know many Applebee's restaurants have Flapjack Fundraisers on Saturday or Sunday mornings? They provide all the food, flyers and clean-up and charge only $2 per person. You simply provide enough volunteers to work as servers! If you charge $7 to $10 per plate, you earn a $5 to $8 profit per person.

The campaign log-in section of our website lists a variety of restaurants that encourage organizations to fundraise, such as Applebee's and IHOP. Some restaurants will donate a percentage of their sales for an evening. The key is to go to your city's most popular restaurants and ASK them for their help.


Monday, July 19, 2010

Leukemia & Lymphoma Facts

• Someone is diagnosed with a blood cancer every 4 minutes.
• About 140,000 people were diagnosed with leukemia, lymphoma or myeloma in 2009.
• Leukemia, lymphoma and myeloma will cause the deaths of more than 50,000 people in the United States this year.
• 146 people die every day from a blood cancer.
• Leukemia causes more deaths than any other cancer among children and young adults under the age of 20.

Thursday, July 15, 2010

NFT Celebrates Its 27th Anniversary!

In 1983, three caring and compassionate women read about a young girl who needed a liver transplant but could not afford the procedure. These women--Mary Clouse, Liz Hull and Elise Waldheim--worked hard to raise funds for the transplant and related expenses, and their tireless dedication contributed to the patient´s successful transplant. And that’s how the Liver Organ Transplant Fund began.

Other transplant candidates soon began contacting them for assistance, and it became evident that transplant candidates across the country would benefit from such services. The organization became the Organ Transplant Fund to reflect the many different types of transplants represented.

In 1998, the board of directors voted to change the name to the National Foundation for Transplants to better convey the organization´s national reach and to clearly include patients needing tissue, bone marrow or other transplants.

What began as a local endeavor has evolved into an organization benefiting thousands of organ and tissue transplant candidates and recipients. NFT's fundraising campaigns have generated more than $56 million to assist patients during their transplant journey, and NFT assists more than 1,000 patients!

We look forward to many more years of helping transplant patients across the country raise the funds they need to receive a second chance at life.

Wednesday, July 14, 2010

Former University of Memphis Basketball Player Needs Your Help

For four years, Willie Kemp gave his heart and soul on the basketball court for the University of Memphis. Tiger fans and the city of Memphis rallied around him, cheering him on night after night at the FedEx Forum. Now, Willie needs your help.

Willie's mother, Maxine Kemp, is battling polycystic kidney disease (PKD), and doctors have said a kidney transplant is critical to her survival.

A mom to three sons--Jermaine, Willie and Quintavius--she remains strong and determined to overcome this battle for them. She loves to spend time with her boys and was Willie's biggest fan when he played basketball at the University of Memphis. More than anything, she dreams of the day when she won't be in constant pain. Maxine is passionate about giving back to the community and helping others in need, but now she must rely on the kindness of others.

A kidney transplant costs approximately $250,000. And that's only the beginning. Even with health insurance, Maxine faces significant medical expenses related to her transplant. For the rest of her life, she will need follow-up care and daily anti-rejection medications. The cost of post-transplant medications can range from $2,000 to $5,000 per month--and they are as critical to her survival as the transplant itself.

In fact, before Maxine can even be added to the transplant waiting list, she needs to raise $2,000 for a hospital deposit.

Tiger fans, now is your time to help! Visit the NFT website to read more about Maxine and make a donation to NFT in her honor.

Tuesday, July 13, 2010

Vote for NFT in Community Security Contest!

Community Security is a local security company in Memphis that donates 10-15% of their proceeds to nonprofit organizations that have partnered with them. When someone signs up with Community Security for their security system, they select a charity, and 10-15% of their bill is donated directly to the charity.

Right now, Community Security is having a contest on Facebook! They’re asking people to visit their page and make a post about why they like one of the charities. Those posts will be tallied as votes, and at the end of the month, the charity with the most votes will get $500.

Only one vote per person, so please spread the word! If you’re on Facebook, please visit their page and post a comment, and pass the word to your friends.