4th annual Jackson Geiser Memorial Toy Drive commences

Jackson Geiser Memorial Toy Drive 2022


CINCINNATI (Nov. 12, 2022) –– The fourth annual Jackson Geiser Memorial Toy Drive (JGMTD) officially commenced today in support of patients at Cincinnati Children’s Hospital Medical Center (CCHMC) during the holiday season.

After raising a record $3,807 in 2021, the JGMTD will once again fundraise exclusively online in 2022 to benefit CCHMC’s Holiday Bundle campaign.

Cincinnati Children’s Hospital Medical Center Holiday Bundle Campaign


Holiday bundles are age-specific packages gift-wrapped by CCHMC staff and directly distributed to child patients in December. The bundles are filled with books, toys, games and activities carefully selected to inspire kids of all ages to play and create.

Based on last year’s donation figure, the JGMTD has set an aggressive $4,000 fundraising goal for 2022. The JGMTD is calling on everyone to bring joy to sick kids this holiday season by contributing to this year’s campaign. While each holiday bundle costs $50 — gifts of any size make an impact.

Donations to the JGMTD can be made at bit.ly/JacksonGeiserToyDrive22. To ensure bundles are delivered to patients by Christmas, please place your donation by Dec. 18.

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About the Jackson Geiser Memorial Toy Drive
The Jackson Geiser Memorial Toy Drive (JGMTD) was established in 2019 by Jeff and Nikki Geiser in memory of their son Jackson, who passed away in 2018 after one month of age due to complications arising from chromosome disorder trisomy 13. Since JGMTD’s establishment, more than $6,400 in donations to Cincinnati Children’s Hospital Medical Center’s (CCHMC) holiday toy campaigns have been raised. In 2019, the JGMTD collected and donated 100 gifts totaling $1,500 in value. When online donations were exclusively accepted by CCHMC in 2020 and 2021, the JGMTD raised $1,180 and $3,807, respectively. To donate to the 2022 JGMTD, visit bit.ly/JacksonGeiserToyDrive22.

2nd annual Jackson Geiser Memorial Toy Drive underway

The second annual Jackson Geiser Memorial Toy Drive is underway but looks slightly different from last year.

Cincinnati Children’s Hospital Medical Center is not accepting in-person donations this year due to COVID-19. So, this year, the Jackson Geiser Memorial Toy Drive is raising money directly for the Cincy Children’s Holiday Bundles Campaign.

Holiday Bundles Campaign
Cincy Children’s created age-specific holiday bundles (valued at $50 each) that will be purchased, gift-wrapped, and distributed to patients during the holiday season. Any amount you can donate helps!

Here are the bundles:

  • Beaming Baby Bundle: For newborn to 2, includes a variety of baby items and toys
  • Toddler Trinkets and Playful Preschool Pack: For ages 2 to 5, includes a variety of age-appropriate learning toys and books
  • Spectacular School Age Sack: For ages 6 to 11, includes a variety of crafts, toys and activities
  • Terrific Teen and Young Adult Treasures: For ages 12 and up, includes a variety of teen-friendly activities and games
  • Soothing Sensory Specials: For children of all ages with sensory challenges, includes a variety of items that provide sensory stimulation through touch, sight and sound.

Thanks to you, last year’s inaugural Jackson Geiser Memorial Toy Drive was a big success. We collected and donated 100 items valued at more than $1,500 in merchandise for Cincy Children’s.


With your help, let’s top that number this year! Every gift, no matter the amount, makes a difference.

Love,
Nikki & Jeff Geiser
Jackson’s mom and dad

Inaugural Jackson Geiser Memorial Toy Drive yields 100 gifts for CCHMC

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The inaugural Jackson Geiser Memorial Toy Drive was a big success, with 100 items valued at more than $1,500 in merchandise gifted to Cincinnati Children’s Hospital Medical Center.

Nikki and I delivered the donations to CCHMC on Friday, Dec. 20, 2019, just in time for Christmas.

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We’re grateful to everyone who donated! The response was more than we expected. It was heartwarming to witness so many people willing to spend their hard-earned money on gifts for some of the world’s most vulnerable kids. The fact that it was done in memory of our son Jackson made it even more special to us.

With the first Jackson Geiser Memorial Toy Drive under our belts, we’ve learned ways to improve it for next year in hopes of making it bigger and better. Stay tuned and thanks again!

Note: 10 of the 100 items were Christmas gifts purchased on behalf of Jackson in 2018, when the idea of donating toys to CCHMC originated but before the Jackson Geiser Memorial Toy Drive was created.

Announcing the inaugural Jackson Geiser Memorial Toy Drive

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Update 12-16-2019: We received confirmation that we can deliver the toy donations to Cincinnati Children’s Hospital on Friday, Dec. 20.

To honor the memory of our son Jackson Geiser (May 4, 2018-June 3, 2018), Nikki and I are putting together a toy drive benefiting Cincinnati Children’s Hospital Medical Center.

The holidays can be an especially difficult time for children in the hospital. And since we will never have the opportunity to watch Jackson unwrap Christmas presents, we’ve decided to take the love we have for our firstborn child and channel it to other kids dealing with health problems during what is supposed to be the most wonderful time of the year.

We’re collecting toys that are specific to Jackson’s age (he would be 18 months old right now) and donating them to Cincinnati Children’s.

Cincinnati Children’s has specific guidelines on the toys that are accepted for donations. For example, all donations must be brand new, odor-free, in original packaging and purchased within the last 3-6 months. No stuffed animals and plush toys. Please do not gift wrap your items.

Amazon Gift Registry AddressTo make a donation, visit the Amazon Wish List for the Jackson Geiser Memorial Toy Drive. Select “Gift Registry Address” as the shipping address when checking out (see screenshot to the right). The items on the Amazon Wish List come directly from Cincinnati Children’s list of approved toy donations.

If you want to donate something that’s not on the Amazon Wish List, please make sure it meets Cincinnati Children’s toy guidelines (https://www.cincinnatichildrens.org/giving/gifts/items/toys).

The deadline to make a donation to the Jackson Geiser Memorial Toy Drive is Thursday, Dec. 12, 2019 (items must be received by this date). I am going to arrange for dropping off the toys at Cincinnati Children’s Hospital Medical Center on Friday, Dec. 13, 2019.

To make a donation, click here: http://bit.ly/JacksonGeiserToyDrive.

One year ago today: Jackson, our little fighter, went to Heaven

One year ago today, on June 3, 2018, my son Jackson passed away after 31 days of life. The following is an excerpt from the PostHope.org page that my wife and I created last year when Jackson was in the NICU. This is the first time these words have been shared publicly as our Post Hope page was password protected and only shared with family, friends and coworkers.

Jackson resting

After coming home from the Good Samaritan Hospital Neonatal Intensive Care Unit on June 2, having a ventilator removed and breathing on his own for more than 29 hours, our firstborn child Jackson gained his baby angel wings on Sunday, June 3, the 31st day of his life.

In true form, Jackson fought until the very end until his body could no longer properly oxygenate and his heart stopped beating at 7:18 p.m.

From Saturday night into Sunday morning, Nikki and I revived Jackson about nine times, whenever his oxygen saturation level would dip below 70 percent on his pulse oximetry monitor.

As time went on, his dips were becoming more and more frequent. We were doing everything that we could to snap him out of these spells, including chest compressions and infant CPR. Each time he managed to come back; however, there were several incidences where we thought he was at the end.

At noon on Sunday, a palliative care nurse from Starshine came to our house to check on us and see how Jackson was doing. She arrived during one of the times Nikki and I were reviving Jackson and she immediately began to tear up when she saw the scene of us desperately trying to keep him alive.

She told us that putting ourselves through Hell to keep Jackson alive is not comfort care. She suggested that we take Jackson off the monitor and just simply enjoy our time with him.

While we were initially hesitant to take him off the monitor, after a couple more revival episodes, Nikki and I agreed that it would be best for Jackson if we removed every wire off of him – the pulse oximetry monitor and the oxygen nasal cannula – and just let him enjoy his time free of cords. He finally had nothing on his beautiful face!

During his remaining hours, Nikki and I took Jackson outside on a gorgeous warm sunny day. Holding him in our arms, we took him first to our backyard deck and then to our front porch. You could tell he was truly enjoying the sunshine and looked so much at peace whenever the breeze touched his face. It was truly a moment neither one of us will ever forget.

After having Jackson outside for a while, we brought him upstairs to our bedroom and just laid in bed with him for an extended period of time. Once Nikki and I started to doze off, we decided to bring Jackson back downstairs and sit with him on the couch where he ended up taking his final breaths a couple hours later.

To give you an accurate picture of how life was like for Jackson, Nikki and me during the time Jackson was home, watch this 2009 video produced by the Dallas Morning News called “Choosing Thomas — Inside a family’s decision to let their son live, if only for a brief time.”

Nikki and I are truly devastated by the tremendous loss of our firstborn child. There have been more tears shed in the last couple days than at any other time in our lives. This is something we will never get over; it’s something we just hope to learn to live with.

Nikki and I are comforted in knowing that Jackson is now in a much better place. He’s with his grandpa (my dad) in Heaven, along with his great grandparents and other relatives. He will never have to go through another medical procedure and he will no longer be held back by an evil chromosome disorder.

We have no regrets with our decision to bring Jackson home on comfort care, rather than send him to Cincinnati Children’s Hospital Medical Center where he was facing a year-long hospital stay. Looking back on it now, it seems unlikely to think Jackson would have been able to survive that long, regardless if he was in the hospital.

The fact that Jackson was able to live 31 days and spend his last moments with his family at his house is a huge blessing to Nikki and I. He defeated so many odds that we will always refer to Jackson as “our little fighter.”

Contribute to the Good Sam NICU
Donations in memory of Jackson Geiser can be made to the Good Samaritan Hospital Neonatal Intensive Care Unit online at bit.ly/InMemoryofJackson or by calling 513-862-3742.

Click here to view Jackson’s obituary published June 6, 2018, in The Cincinnati Enquirer.

Here’s how you can recognize Trisomy 13 Awareness Day

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Nikki and me loving on Jackson at the Good Samaritan Hospital NICU

Today (March 13) is Trisomy 13 Awareness Day –– a day that will forever live in infamy in my household.

Trisomy 13, also known as Patau Syndrome, is an extremely rare chromosome disorder that affects about one in about 10,000 babies. Trisomy 13 is in the same family of chromosome disorders as Trisomy 21, most commonly known as Down Syndrome.

Whereas many people with Down Syndrome live independent lives and have an average lifespan of about 60 years, the outcome for Trisomy 13 is typically fatal, with the average lifespan about 2.5 days.

My wife Nikki and I learned just more than a year ago, on March 7, 2018, that our then-unborn son Jackson had Trisomy 13.

In just a matter of days, we went from feeling the excitement of the arrival of our firstborn child to the horrors of a trisomy 13 diagnosis. On March 5, at 26 weeks of pregnancy, Nikki went to Good Samaritan Hospital in Cincinnati for a full anatomy ultrasound scan. This was of course the first and subsequently only appointment that I had not attended. While she was in the ultrasound room, I was at work having a routine work day. That is until my phone rang; it was Nikki calling me and I immediately began to worry that something was wrong since I knew that her appointment had just started. When I answered the phone, I was on the speaker phone with both Nikki and the maternal fetal doctor, who informed me that she spotted abnormalities on the ultrasound, in Jackson’s heart and feet, an indicator of a possible chromosome abnormality.

The next day Nikki had an amniocentesis performed to test Jackson’s chromosomes, and one day later on March 7 we met with a genetics counselor who told us initial testing showed that Jackson had trisomy 13.

This news was devasting and heart breaking; we knew nothing about this disorder other than that we were told that Jackson would most likely be a stillbirth.

Imagine being told that your child is going to die before his birth.

With 13+ weeks before Jackson’s due date, needless to say the remainder of Nikki’s pregnancy consisted mostly of anxiety and hopelessness as we feared the worst.

Thankfully there are support organizations for people who are facing a Trisomy 13 diagnosis.

The Support Organization for Trisomy (SOFT) was a tremendous help to us. They provided answers to many of our questions and helped us prepare for Jackson’s arrival. They provided us hope that Jackson was not going to be a stillborn as there are many examples of Trisomy 13 children who’ve lived for several years. Heck, there is even a woman in the SOFT community who just turned 40 years old. How awesome is that?

The biggest support that SOFT provided to Nikki and I was in the preparation of our birthing plan. They helped us dot every I and cross every T, ensuring our birthing planned was as detailed as possible in order to give Jackson the best chance to, not only survive the delivery, but also to live as long as possible.

Thanks to the birthing plan and the awesome NICU staff at Good Samaritan and Cincinnati Children’s Hospital, Jackson defied the odds and lived 31 days, May 4 through June 3, 2018. This is despite Jackson arriving early at 34 weeks and 3 days, and despite being a male (boys with trisomy tend to have worse outcomes than girls).

While we are absolutely devasted that Jackson is no longer with us, Nikki and I are so thankful that we got as much time with him as we did. Many Trisomy 13 families don’t get that much time with their newborn child.

So, what can you do to observe Trisomy 13 Awareness Day?

There are many simple ways anyone can recognize this meaningful day. The first is simply to wear yellow on March 13. Another way is to reach out to anyone you know that’s been impacted by a Trisomy 13 diagnosis. A simple call, text, Facebook message, etc. would be greatly appreciated. A third way is to publish a social media post using the hashtag #trisomy13awareness. And if you’re feeling generous, you can donate to nonprofit organizations specific to Trisomy 13; there are several to choose from, such as SOFT, Hope for Trisomy 13 and 18, and the International Trisomy 13/18 Alliance.

My first Father’s Day without my father

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Today is my first Father’s Day without my father.

This is a hard reality. My emotions are raw, ranging from depression to pride.

My father Bill Geiser passed away in January 2017 after a hard-fought battle with esophageal cancer.

Not a moment has passed without me thinking about him and missing him. Dad and I had a special bond. He was more than just my father; he was my best friend.

Like I said to the crowd who gathered to pay their respects during his eulogy, “I won the Dad Lottery.”

I could not have asked for a better mentor, supporter, teacher and friend. Dad was always there for me. From when I was a small child teaching me how to swing a baseball bat, to an adolescent when he showed me the proper way to parallel park, to adulthood when he advised on the best techniques to paint the interior walls of my first house, my Dad was always there for me.

We bonded over everything, from cars, politics, and mainly sports. As Cincinnati natives, we spent countless hours watching the Reds, Bengals (mostly to get a laugh) and Bearcats basketball and football.

As I look back on the impact Dad has had on my life, the biggest lesson I have learned from him is the importance of being a good, honest family man.

My dad was married to my mom Dianna for more than 36 years when he passed away. They were unequivocally committed to one another and to their family. They were inseparable. Watching their love grow stronger over the course of three decades has been an inspiration to me when it comes to my own marriage of almost one year to my wife Nichole.

Many people do not know this, but Nikki was gracious enough to move up our wedding date by one whole calendar year due to my father’s illness. Nikki and I got engaged in May 2016 and no more than three weeks later we found out that my dad had cancer. Once we officially got the diagnosis that it was stage four E.C., we decided to get married on July 15, 2016, instead of July 15, 2017, in order for my Dad to be there and share that experience with us. He actually delayed his first chemotherapy treatments until July 18 in order to be at his best for our wedding.

I will forever be grateful to Nikki for being so considerate and understanding, sacrificing a traditional, big wedding for a small, intimate gathering of parents, grandparents and siblings at a public park in Cincinnati, Ohio. It was a beautiful day, with my Dad serving as best man, groomsman and ring boy.

Not only was my Dad tremendous to his own family, he was a “saint” to his mom, my grandmother, Jean. For years, I witnessed my Dad spending much of his time with Jean, who by the Grace of God spent her remaining years living independently in a two-family house that she purchased, despite having a prosthetic leg. If my Dad didn’t stop by her house every day, it was certainly at least every other day. Sometimes it would be to do some work on her house; him being a master craftsman and carpenter for over 30 years helped. Other times, it would simply to stop by and spend some time laughing with her.

I was not the only person who noticed how dedicated Dad was to his mother. The property managers of the house adjacent to Jean’s saw it. In the months since Dad’s passing, my mother reached out the property managers to gauge their interest in purchasing Jean’s home. During this exchange, the property managers revealed to Mom that they referred to Dad as “St. Bill” for his treatment of Jean. This filled my mom’s heart with joy and pride. That’s the type of person Dad was.

One of the things that I miss the most about Dad is his terrific sense of humor. It was one of his gifts and allowed him to forge so many friendships throughout his lifetime. His quick wit and smart-ass remarks could put even the most uptight person into tears of laughter.

While I may not be able to spend another Father’s Day with Dad playing catch in the outfield of Great American Ball Park (which we did in 2015), sharing a few beers in his immaculately-kept backyard, or later on in the future watch him play with his grandchild(ren); I will always spend it remembering his best qualities and how lucky I was to have him as my Dad for 33 years.

My Dad has inspired me to dedicate my life to being a good and better man to my wife, Nikki, and our family.

If I turn out being even just half the man my father was, then I will have felt like I have achieved the impossible.