Posts Tagged ‘support’

Doctors gave us a scare!

Tuesday, May 10th, 2011

Hello family and friends,

I hope this beautiful weather finds you well and that you are beginning to see the signs of a beautiful spring. 

Aaron is doing well. We had a scare on his biopsy in February. It showed a slight rejection. Can you imagine? What would you have done?

My mind raced back to the months we spent in The University of California, San Francisco (UCSF) in the ICU and all the sleepless days and nights in the hospital here and in Los Angeles. All those hours he spent hooked up to the dialyses machine — that noise is still so clear in my head. I remember Aaron getting on the transplant list and waiting and waiting for our phone to ring.

In April, in the same sentence the Dr. saw some rejection he also said, “Well, if his kidneys reject we just will get him re-listed we don’t want to loose his heart, but his kidneys will definitely go first.”

HUH? I almost fell out of my chair — I couldn’t even respond to him. We spent a month of hell praying that the results would be clear. None of the other families that we had met like Aaron, had gone through this, but none of them were two major organ transplants either.

His cardiologist decided to wait just one-month before repeating the biopsy. The doctor repeated the biopsy in April; it came back with a perfect result.

The doctors seem to think it was a result of some changes they had made in his anti-rejection medication, at the time they had drastically reduced the amount of several, in order to save his kidneys any damage.  So, he is on a very altered treatment path than most other transplant patients. That being said, he is monitored more closely than most other transplant children are.

He will continue his monthly IVIG treatments, along with weekly clinic appointments.

He celebrated his 6th birthday on April 9th, with very few guests due to his immunosuppression. We thought he would be ready for school this spring but his doctors have said to have him wait until the beginning of next school year. He is disappointed. Aaron is really looking forward to going to school and doing normal activities that other children are able to do.

Our family has grown so much wiser our relationship together has grown and our relationship with God is so much stronger. When you experience pain like no other and grief beyond imagination, you see that the time you have to spend is precious — every minute should be enjoyed and savored — whether at work or with your family, make the most of your life now. Don’t wait for something outside of yourself to make you happy — be happy now.

Our webpage is still up and we would greatly appreciate any donations you could pass on to us, through either the website or the Aaron Tanner heart foundation. There are no fundraisers planned and we have no other donations coming in. Financially it has become very difficult, the money you donate will help Aaron to thrive with this gift of life he has been given.

Organ-ize The Planet

Monday, August 31st, 2009

The following is a letter of support that she received today that she would like to share with everyone…

Hi Elizabeth,

I understand you may be in LA right now at UCLA Medical Center and we want to let you know that Aaron and the family are in our prayers.

My name is Mike Corbitt and I just read the article about Aaron in the local Contra Costa Valley Times newspaper. I also saw an article you wrote in the 110 magazine and was touched by both.

Twelve years to the day, my daughter Delaney was almost 3-years-old and sitting in Packard Hospital at Stanford recovering from her kidney transplant. We know what Aaron is going through is very traumatic not only on him but the whole family and we want to let you know that our prayers are with him and the entire family.

We have started a non-profit called Organ-ize The Planet and are working to get the word out on organ donation. I will try to get something up on my website but wanted to get your permission whenever it is convenient for you.

You sound like an incredible mom with a lot of spirit literally and figuratively and we will say a special prayer for you as well. We know that trying to keep a 4 year old preoccupied while in a hospital environment is nearly impossible, and the small children can get very testy.

Delaney used to flat out tell the doctors (only certain nurses)  they stunk and go away and other really nice things, which used to make us chuckle months later.  :)

We organize a walk across the Golden Gate Bridge and last year we dedicated it to Allie Von Zup who had a heart transplant in LA, (I think UCLA) and her brief story is on my web site. Her older sister Missie also needed a heart transplant and both transplants were very successful.

Early next year in April or May we will have another walk across the Golden Gate Bridge and I would like to dedicate it to Aaron. So, we expect Aaron the entire family to join us for our walk that we do in conjunction with the California Transplant Donor Network.

Hang in there …keep the faith and keep doing exactly what you are doing.

Love Mike & Family

Michael Corbitt,
Retail Portfolio Manager,
Northern California Region
Harsch Investment Properties

Preschooler in need of double transplant

Monday, August 10th, 2009
By Ruth RobertsAaron Tanner, 4, is in need of a heart and kidney transplant. He is currently undergoing tests and treatment at UCSF to stabilize his condition.<br><i>Photo courtesy of Laura Page</i>

Aaron Tanner, 4, is in need of a heart and kidney transplant. He is currently undergoing tests and treatment at UCSF to stabilize his condition.

Aaron Tanner is a cherub-faced 4-year-old with a shock of white-blond hair and a ready smile. On the surface, the Brentwood boy looks like any other high-spirited, carefree preschooler, but it’s there that the similarities end.

Aaron was born with a heart that functions only on the right side. The condition kept the newborn in the hospital for six weeks before he was declared strong enough for his parents, Elizabeth and Kevin Tanner, to take him home.

But only a week later, the Tanners’ 2-year-old son Ethan suddenly developed flu-like symptoms. Unable to calm the agitated toddler, they rushed him to the hospital, where he died a few hours later from a rare heart disease called Pertrophic Cardiomypathy; a typically genetic disease that often strikes without warning.

The Tanners now face yet another heartbreaking challenge: last week, doctors discovered that Aaron –who has undergone seven open-heart surgeries since he was born – must now undergo a simultaneous heart and kidney transplant. Renal failure has placed too much stress on the boy’s heart, and without the rare double-transplant surgery, Aaron’s chances of survival are low.

“Aaron is currently at UCSF undergoing tests as everyone just tries to figure out what they are up against,” said Laura Page, executive director of Kids Helping Kids, who recently heard of the Tanners’ plight. “This surgery is so rare that they have teams within teams of doctors working on this. We’re just trying to get the word out and do what we can to help.”

Help will be coming in part through a fundraiser, to be held sometime next month, that Page is organizing. According to Page, the Tanners’ medical bills are stacking up, and because of the debt they incurred with the death of Ethan, the family is facing foreclosure on their home.

“Aaron takes eight different medications a day to regulate his heart and blood pressure, and to prevent water from building up around his heart,” said Page in a recent e-mail. “Just one (of the medications) costs $7,000 a month. They have a cap on their insurance, which they are dangerously close to (before this recent hospital stay and proposed surgery). They really need our prayers and big miracles.”

Aaron and his mom are expected to remain at UCSF for the next few weeks as doctors develop a plan and Aaron undergoes kidney dialysis. He will also be given a medication designed to ease the blood flow and keep his blood pressure in check.

Despite her son’s dire situation, Elizabeth remains strong and optimistic.

“Aaron is in good spirits, as always,” she wrote in a blog earlier this week. “He is a bit sleepy, but is still able to give the staff a run for their money. We are waiting and praying. I can’t thank everyone enough for their support and prayers, blogs and notes of love and encouragement. It feels like our whole community is really pulling for us and I know God hears our prayers; you can feel it, it’s so evident in all that is happening.”

For those able to help the Tanner family, a few options are available: a fund has been set up at the Bank of Agriculture on Balfour Road in Brentwood.