Friday, January 24, 2020

Lexington teen continues road to recovery following dual organ transplant

Marquis Davis has been at Cincinnati Children's Hospital since his dual organ transplant on Dec. 1, 2019.  (Source: https://foxlexington.com)
LEXINGTON, Ky. (WDKY) - Less than two months after a heart and kidney transplant, doctors at Cincinnati Children's Hospital are planning to discharge Lexington teen Marquis Davis.
"Overall, they're happy,” Davis’ sister Porsha Jackson said about his doctors. “They've been pleased with everything they've been seeing."
Davis has been in the hospital since his surgery on December 1, but he's not headed home just yet. Davis and his mom will be staying at the Ronald McDonald House to make sure he's in close proximity to the hospital.
"He has to be there every day,” Jackson said. “He has to do lab work and make sure everything stays consistent, stays the same."
It's not a totally unfamiliar process for this family, as Davis was diagnosed with hypoplastic left heart syndrome and had his first heart transplant at only three years old.
"It's more intense because it was two organs instead of just one,” Jackson said. “Last time, it was just the heart, now it's a kidney and the heart, so I think there's a lot more that he has to do than he did last time."
Last time, Davis' body rejected the organ. So, as Davis pushes through appointments, lab work, and cardiac rehab, his family is pushing the fear of rejection a second time to the back of their minds.
"That's something they've got to tell us, but you don't want to think about,” Jackson said. “But, he's been fighting this long, so I think he'll be alright, he's just ready to come home."
Davis' family said if his progress continues, he should get to come home sometime in March.
Meanwhile, the Consolidated Baptist Church is holding a service of celebration for Davis' continued recovery on Sunday, Feb. 2 at 3:30 p.m.

Monday, March 11, 2019

When My Daughter Joined The Heart Transplant Wait List, We Entered A New World

My youngest began getting sick over the summer, just a couple weeks after her first birthday. My “mom intuition” started to nag at me that something wasn’t right with her. She was acting differently. Something was off. Her appetite started to decrease, her diaper output became minimal, she was breathing quickly and she was more tired than usual. After a quick trip to an urgent care, I was assured that she was just teething and it would pass. Days went by and that “mom intuition” continued to weigh on me so we made an appointment with her pediatrician shortly after.
With a single diaper in tow (fourth child problems), I thought I would be back in an hour with some medications to fix whatever was going on with my baby girl. After multiple tests and a chest x-ray, we were immediately sent to the local Children’s Hospital Emergency Room. I was still in denial at this point. I assumed my daughter just needed some IV fluids or some brief monitoring and we would be home later in the evening or worst case, the next day. But then it was discovered that our baby girl had a very serious heart condition and would need to be admitted to the Pediatric Intensive Care Unit.
Source: https://imgix.romper.com
The ER cardiologist was kind but didn’t beat around the bush. He spoke slowly, knowing it would be hard to comprehend what he was going to say. He said my daughter was in heart failure and she was going to need immediate hospitalization. He went on to say she had a one-in-three chance of surviving. My mind wasn’t able to process this devastating news. I was in complete shock. I felt numb. I felt sick. I wasn’t at all prepared for any of this. For heaven’s sake, I brought only a single diaper. All I could do was sob while my sick baby lay lethargically in my arms. We were wheeled out of the emergency room with two broken hearts that day.
We spent 28 very long days in the hospital so our daughter could receive IV medications. After four weeks, we were sent home on oral medication, hoping it would be enough to manage her newfound heart condition. But we would soon find out that her medicine regime wasn’t working.
"WE CAME TO THE HOSPITAL NOT KNOWING HOW LONG OUR STAY WOULD BE. WE WERE GIVEN AN AVERAGE WAIT TIME RANGE BUT WE’VE SURPASSED IT NOW."
For eight stressful weeks at home, we watched our daughter continue to deteriorate. Then we were admitted back into the PICU, where she was placed on the heart transplant waiting list. We had no other options. Her heart was failing because the oral medications weren’t enough.
I’m writing this in our hospital room, where we’ve been waiting for the last 122 days. We came to the hospital not knowing how long our stay would be. We were given an average wait time range but we’ve surpassed it now. I’d be lying if I said it wasn’t hard living in a hospital. The days are long, boring and I feel like I’m in a horrible version of Groundhog’s Day. Same routine, different day. There’s never a weekend to relax at home to decompress and gear up for another week. It’s living in limbo all day, every day until we get the news.
Source: https://imgix.romper.com
It almost feels wrong waiting for another young child to pass away so that my daughter can have a second chance at her own life. I already ache and have cried many tears for the unknown family who will unselfishly donate their child’s organs so that my child and others may live. Even though I don’t know who they are, I pray for them as we wait. They’re racing the clock just as much as we are, except they probably don’t realize it. Her heart will likely come from an unexpected death, which just makes it that much harder.
I spend a lot of time processing this experience. It’s been the hardest thing I have ever had to do. I’ve felt a lot of sadness and guilt when it comes to using another child’s heart to replace my daughter’s broken one. But I have to remind myself that my daughter isn’t taking anyone’s life. Her donor’s family will choose organ donation. And because of their loving and thoughtful decision, my daughter will be given the most precious gift anyone could receive. The gift of life. It will be something we will never take for granted and we’ll strive to honor her donor’s life by taking care of her new heart to the best of our ability.
While this process is incredibly draining, in almost every way, I try to turn my thoughts away from negativity. It’s so easy to get caught up feeling sorry for yourself. It can and will swallow you whole if you let it. I’ve found that it makes the days more bearable when I count my blessings and have an attitude of gratitude. Even during the darkest days, there’s always something to be thankful for. And finding those things actually brings me happiness and peace despite our circumstances.
Hardships don’t mean we have to be miserable until they’re over. We can and should find joy, no matter how difficult life can be. There will always be things out of our control, but we always have the ability to choose our attitude and reactions. It can often feel like our trial will never end, but I remind myself that it’s just temporary in the grand scheme of things, and I look forward to the day when this is all a distant memory. Until then, I’m choosing joy.

Thursday, January 31, 2019

Miracle birth for overjoyed mum who had heart, lung and liver transplant


Lucinda, Damon and Angus (source:https://www.mirror.co.uk/)

Living heart donor Lucinda Simpson is believed to be the only woman to have received, given and created the gift of life.

Having been told she would never have a baby, the 38-year-old became the first woman to give birth after having a triple heart, lung and liver transplant.

It is not the only record under her belt. In 2005, Lucinda also became one of just four successful living heart donors.

All of them had “domino” transplants, where their hearts were gifted to others while they were receiving donor organs.

Doctors believe Lucinda, mum to nine-month-old Angus, is a one-off.

She says: “When Angus was born last April, he became the only baby in the world to be born to a woman after a heart, lung and liver transplant.”

Yet Lucinda is well aware of the thousands who are not so fortunate.

She hopes the Mirror’s Change the Law for Life campaign for an opt-out organ donor system inspires the rest of the world. “Without my donor, none of this would have been possible, which is why I’m backing the Mirror campaign to introduce the opt-out system,” she says.

“Sadly, so many lives are lost due to long waiting times for transplant surgery in the UK.”

Lucinda, from Queensland, Australia, was born with cystic fibrosis, which damages the lungs and digestive system, and always knew she would one day need a lung transplant.

“If you think of lungs as the size of a two-litre milk container, I was breathing 30ml instead of 2,000ml,” she says.

“I had to stop ­working, which I hated as my brain was fine. It was just that I couldn’t keep up. I couldn’t vacuum, make the bed or even do the dishes.”

Lucinda, 38, was born with cystic fibrosis and underwent a heart, lung and liver transplant
(source:https://www.mirror.co.uk)
Lucinda’s condition got so bad due to all her heavy medication that, by her early 20s, her liver had deteriorated.

Doctors opted to replace her heart as well as her lungs and liver. She says: “My heart worked perfectly fine, but the doctors explained it would be easier to replace all three organs in one go.

“It was easier to do the surgery like a car engine: put the heart, lungs and liver in as a block. You just lift one lot out and put the other lot in, so there are fewer connections.”

Before the surgery Lucinda started dating her future husband, Damon. She says: “Other blokes I’d dated were like, ‘She’s just too high maintenance, I don’t want to deal with that’.

“We’d only been seeing each other for a few weeks when I told him all about my condition and what was in store.

“But he said, ‘Even if you had no arms or legs and you were just ahead, I’d buy you awesome hats for Christmas’. I knew then he was a keeper.

Angus (source:https://www.mirror.co.uk)

“I hadn’t even made it to the operating table yet, but I’d already given my heart away, to Damon.” Ten months later, on her 24th birthday, Damon proposed.

The pair asked Lucinda’s pre-transplant team if she would ever be able to carry a baby. She says: “We were told it was unlikely I’d survive long enough to have a family.”

Then in June 2005, four months before their wedding, the couple got a call as they were having dinner.

Lucinda says: “I was told I was gett­ing my transplant that night. Damon told me he loved me, then I was wheeled into the operating room while he waited with my parents, Kaylene and Jim.”

A recipient was found for Lucinda’s healthy heart. “It was incredible, but it was bittersweet.

“To give me a chance, someone had lost their life,” she says.

Having been in and out of hospital all her life, Lucinda was not fazed as she waited to be put to sleep. “I was looking around fascinated at all the surgical instruments asking, ‘What does that do?’

“They’re like, ‘That’s going to separate your rib cage. This machine will be your heart and lungs for you as we operate’. I thought that was so cool.

“I even asked to keep my old organs in a jar, but they suggested I donate them to medical science, which sounded like a much better idea.”

The 12-hour operation was a success and Lucinda was able to go ahead with her wedding, exactly two years to the day she first met Damon.

Five years later, she told her doctor of her hopes of getting pregnant.

“By then, he thought carrying a baby wouldn’t be a risk to my life. But it wasn’t as easy as just trying to fall pregnant,” Lucinda says. Her daily cocktail of medicine had to be carefully assessed to make sure it would not cause birth defects or miscarriage.

Then, Lucinda’s heart, lung and liver function had to be rigorously tested.

Getting ready to have a baby took years. “Pregnancy was not something we were rushing into,” she says. “We were not being irresponsible.”


As the years passed, and she failed to conceive, Lucinda began to lose hope. Then, after their 12th wedding anniversary in 2017, a routine blood test revealed she was pregnant.

“We were both so surprised, Damon and I burst into happy tears,” Lucinda says. “The day before the 20-week scan, on Valentine’s Day, I felt our baby kick for the first time.” Angus was delivered 12 weeks early by emergency caesarean on April 18 last year, 13 years after the transplant.

“We’d been warned that, being a transplant mum, I was unlikely to go to full term. But giving birth at six months was way earlier than we expected,” Lucinda says.

At just 1lb 8oz, Angus was whisked to the neonatal intensive care unit. Lucinda says: “I wasn’t allowed to see Angus for 24 hours. Even after that, I could only place my hands on him.

Lucinda  (source:https://www.mirror.co.uk)
“I just cried. I was so happy to have him, but I didn’t want him to be in a little glass box. I finally got to cuddle him when he was 11 days old.”

The couple were allowed to take Angus home after nearly three months, when he had reached 5.7lbs. He is happy and healthy.

Lucinda adds: “I tease Damon, saying, ‘Do you want to do it again?’ He just replies, ‘I think we’ve been blessed with one’.”

Tuesday, January 29, 2019

Doctors Complete 1st Stem Cell Transplant of the Eye in Kenya

The Healthcare industry in Kenya has experienced tremendous growth and development leading to high levels of practice of technological treatments as witnessed recently.

A recent and first technological treatment procedure involving stem cell transplant for the eye, a highly technical procedure, was successful.

The team of medical specialists that conducted the operation was led by one Mukesh Joshi and conducted the entire process in just under three hours.

Susan Muthoni after the Treatment  (source: https://www.kenyans.co.ke)

Speaking of his professional experience, Joshi had a few words to say about the medical intervention. He indicated, “It was smooth but technically challenging.”

The patient, Susan Muthoni, made history after being the recipient of the first treatment of the kind not only in Kenya but the larger East Africa Region.

Muthoni regained her sight- being able to see with the normal 20/20 vision by the function of the first stem cell transplant of an eye in East Africa.


A look into the background of the patient shows that the patient had normal sight while in high school but her eyes were damaged in a laboratory accident, in 2013, when chemicals spilled onto her face.
Laser Eye-care and Treatment Machine

As for the outcome, her left eye became partially blind while the right one went completely blind.

For purposes of continuing her studies, the special eyesight-enhancing glasses became a necessity for the young lady.

The quest for Muthoni to regain her eyesight was seemingly unachievable and too expensive.


In an interview with The Standard, Muthoni indicated, “I went to Kikuyu Eye Hospital but the doctors said there was not much they could do except give me the enhancing glasses.”

She resolved to travel to India to seek treatment options as a last resort but was advised to get the same in Kenya by a family friend.  

The friend informed Muthoni of a clinic based in Westlands, Nairobi. Little did she know that the procedure would be successful and she would be going down in the nation's history books.



Wednesday, January 23, 2019

Woman Who Underwent Historic Double Transplant Surgery To Get New Kidney


source: https://losangeles.cbslocal.com


LOS ANGELES (CBSLA) — A woman who made history as the first person in the Western U.S. to have double transplant surgeries for her heart and liver will undergo a third transplant Tuesday at Cedars-Sinai Medical Center.

In 1998, Christine Galan made surgical history when she underwent double transplant surgery for her heart and liver.

However, a few years ago, Galan’s kidney started to fail. So she went on to search matching donors, and a perfect stranger volunteered to donate her kidney.


“She is one incredible woman. I mean, I didn’t know her, and she just came forward to give me a life,” Galan said.

Halsey says her faith led her to become a donor for a kidney transplant.

“We’re all human beings, and we all have to do whatever we can to see to the comfort of each other,” Halsey said.

The surgery is scheduled to Tuesday at Cedars-Sinai Medical Center.

source

Tuesday, January 22, 2019

Broomfield man takes first breath of fresh air in years after lung transplant



BROOMFIELD, Colo. -- For Broomfield resident Dennis High, the last couple months of 2018 were filled with swirling doubt.

"I talked to my wife the day before and I thought if it didn’t happen soon, it wouldn’t happen at all," High said.

Doctors didn't know why High's immune system was attacking his lungs, causing them to fail to take in oxygen. He needed to be hooked up to several tanks of oxygen at a time just to take a gulp of air.

After weeks at the top of the transplant list, waiting for the phone to ring, High finally got the hope he's been waiting for: he was getting a transplant.



"That first breath of fresh air was amazing," High said. "Not having to depend on this was really nice. I mean, this was my lifeblood for two years."

Now, High has a second chance and time to spend with his wife and family. After his Lung Transplant surgery, the generosity of strangers took his breath away, with some people anonymously donating thousands of dollars to help pay for medical bills and medication via GoFundMe.

"I couldn’t believe it," High said. "They don’t know me. Really surprised as to how much some gave."



A spokesperson for UCHealth says High's old lung has been donated to a research campus for science.

source

Wednesday, January 16, 2019

Dayton Children’s to perform bone marrow transplants

source: https://www.daytondailynews.com

Children with cancer soon will be able to get bone marrow transplants at Dayton Children’s Hospital, after the hospital starts offering the procedure for the first time.

Hospital officials say it is a first for children in Dayton, who have previously been referred out for stem cell bone marrow transplants to neighboring institutions such as Nationwide Children’s Hospital in Columbus and Cincinnati Children’s Hospital Medical Center.

Now Nationwide Children’s staff are training Dayton Children’s how to perform the procedure in Dayton. Patients will start being treated through the program in February or March.

“Children with cancer, their treatment expands over years, and it’s very important for them to stay close to home where their support network is available,” said Dr. Ayman El-Sheikh, chief of Dayton Children’s pediatric hematology and oncology division.

The procedure includes harvesting a child’s stem cells from their bone marrow before chemotherapy. The harvested stem cells then are returned to the child after treatment is complete to help their body build normal blood cells.

Children who have the major procedure are in the hospital for about two or three weeks, El-Sheikh said.
Emily Springer said her two-year-old son Henry went to Nationwide to have his stem cells harvested in 2018. She said the new program is good for families because in the future it will let children stay closer to home at Dayton Children’s.

Dayton Children’s and Nationwide said this also will create more research opportunities for both hospitals. The hospitals will share physician services and have more clinical trial opportunities.

This bone marrow transplant program is part of an agreement formed in October 2013, where Dayton Children’s and Nationwide work together to share resources, avoid duplication and better use limited pediatric specialists.

Three other initiatives currently operate under this umbrella: a joint outpatient specialty care center and a pediatric practice in Springfield, collaborative on heart services quality initiatives as well as a Lima clinic, and shared services in urology.

“The alliance with Dayton Children’s Hospital is an example of Nationwide Children’s vision to share learnings and discoveries that will provide best outcomes for children everywhere,” said Dr. Timothy Cripe, division chief of hematology, oncology and bone marrow transplant at Nationwide.

Nationwide Children’s Hospital is ranked fifth in the nation in children’s cancer care, according to U.S. News & World Report, which surveys hospital clinical data. Cincinnati Children’s is ranked first.

Along with its overall high ranking for pediatric cancer services and outcomes, Nationwide’s bone marrow transplant program received six out of six points from U.S. News for patient 100-day survival after bone marrow transplants.