Tag: Childhood Cancer Awareness

14 Highlights from My First Year As the Wacky Warriors Tournament Director

14 Highlights from My First Year As the Wacky Warriors Tournament Director

As September (Childhood Cancer Awareness Month) draws to a close, I figure it’s about time I do a recap of this year’s Wacky Warriors charity softball tournament, which took place on September 6th and 7th. For those of you who don’t know, the Wacky (Warriors 

This is My “Why”: I’m Doing It for Them

This is My “Why”: I’m Doing It for Them

My heart is hurting today. Truth be told, it’s hurt a lot off and on for several months. The past few days I’ve been especially down, though. The reason why is a one-word answer, and I bet you can guess it. Yep… Cancer. In our 

22+ Childhood Cancer Charities to Donate to on Giving Tuesday

22+ Childhood Cancer Charities to Donate to on Giving Tuesday

I know. I know you’ve already seen too many ideas for non-profits to donate to this week to count. I know it’s right before Christmas, and odds are good that your own finances are stretched tighter than you’d like. However, I also know firsthand how much charities like the ones I’ve listed below help struggling families. And I know how deeply you care and want to help others.

This is FAR from an exhaustive list of charities…or charities for childhood cancer…or even LOCAL (to Utah) charities for childhood cancer. A few of these non-profits not only help kids going through cancer but also many other children with different abilities and/or life-threatening conditions. Every single charity I listed here, however, is one that I love. Most of them have directly benefited my family. ALL of them have benefited many of my friends and their families.

Without further ado, here are 20+ charities (complete with links) that I highly encourage you to support and donate to…

  1. Alex’s Lemonade Stand
  2. Blue Skies Ministries
  3. Camp Hobe*
  4. Children and the Earth*
  5. Christmas for Cancer Families*
  6. Curesearch
  7. Give Kids the World Village
  8. HayesTough Foundation*
  9. Hug Your People
  10. IronmanQ Foundation*
  11. Jessie Rees Foundation
  12. Leukemia & Lymphoma Society
  13. Lighthouse Family Retreat
  14. Make-a-Wish
  15. Millie’s Princess Foundation*
  16. Monkey in My Chair
  17. Nixon Strong Foundation*
  18. Rally Foundation for Childhood Cancer
  19. Sadie Keller Foundation
  20. St. Jude Children’s Research Hospital
  21. Tiny Superheroes
  22. Tyler Robinson Foundation*
  23. BONUS: Wacky Warriors Foundation*

*Non-profits with ties to Utah

I can’t tell you how much joy and relief several of these organizations have given us. Family retreats that helped us have “normal” vacations without medical worries, camps and events that let our children run around and play with other kids who’ve had similar experiences, amazing gifts and toys that brought smiles to all of our faces… I’m so grateful for people and organizations with hearts of gold. I love this famous quote:

“Be the change you wish to see in the world.”

Mahatma Gandhi

I have several friends who are living through the very depths of Hell right now with their kids’ cancer treatments. Hearing that your child has cancer is Hellish enough, but what these families are battling as I type this is unfathomable. So many people are suffering every day. I wish I could take away their pain—or, better yet, CURE the disease that causes the pain, but that ability lies with someone far greater than me.

That doesn’t mean I/we can’t do anything, though. I love it when I can do anything to help ease others’ burdens. It’s a way I can “pay it forward” in gratitude for where we’re at with Lincoln today—20 months off treatment. We’ve been so blessed.

If you have any extra available funds today, please join me in making a difference. Any amount helps! Please make a donation to one of these incredible organizations, and rest assured that the families it will benefit will be so thankful. 💛

Our Fall Break Gatlinburg/Pigeon Forge Vacation

Our Fall Break Gatlinburg/Pigeon Forge Vacation

For fall break we rented a cute cabin via Airbnb in the Smoky Mountains and had a great time rediscovering Gatlinburg/Pigeon Forge and exploring with my parents. It was everything we’d hoped it would be! We loved the cabin—so much so that Logan still calls 

Lighthouse Family Retreat: Take 2 (St. Simons Island, GA)

Lighthouse Family Retreat: Take 2 (St. Simons Island, GA)

We were fortunate enough to go to St. Simons Island (SSI), Georgia for the second time this past June! If you’ve been following us for awhile, you might remember that in July of 2022, we attended a family retreat on SSI with Blue Skies Ministries. 

Moms Fighting Monsters: A Tribute to My Mom

Moms Fighting Monsters: A Tribute to My Mom

When I was two and three years old, I often excitedly ran up the sidewalk and front steps to a red brick, 1950s bungalow as my mom gathered things from our car. Even though I went there at least a couple of times a week while my mom went to classes at Utah State University, I was always thrilled to hang out with Grandma and Grandpa Ripplinger at their house in Logan. I felt lucky and special because I was the only kid in my family who got to see them so often. My three older siblings were all in school, and my younger sister wasn’t born yet.

Almost all of my earliest memories revolve around Grandma Beth. When my mom went back to college after she was 30, my grandma watched me, and we became the best of friends. She’d always make me lunch—often a peanut butter and jam sandwich, and I’d eat it at their kitchen counter. I believe I inherited my love of cats from her. One of my favorite pictures shows the two of us sitting together in a chair enjoying the company of an orange kitten. I can still quote word-for-word parts of the children’s books we read together. The smell of being in a nursery still takes me back to picking out flowers with her. I can’t see, make, or taste Angel Thumbprint cookies or homemade mints without remembering Christmastime with her. 

Grandpa was always there, too—often either reading or working in his small apple orchard out back. Sometimes I’d swing in their amazing tire swing or ride a pink Hot Wheels on their back concrete slab while he worked. I loved the fall, when I could rake up giant piles of Maple leaves with him. And Grandpa’s dry sense of humor was legendary. 

My family frequently refers back to a memory that took place when my little sister was about three years old. Grandpa had come over for dinner. After dinner my little sister, Katie, kept getting a peanut butter bar, taking one or two bites out of it, and then giving the rest to Grandpa. After he’d eaten three or four peanut butter bars mostly by himself, he said to Katie, “My dear, I don’t think I can stand for you to have another one of those cookies!”

In my early years, I spent most of my time with Grandma, though. One of my favorite parts of the day was when the mail was delivered through the mail slot that opened right into their living room. I’d hear the mailman open the metal mail flap, and I’d race to the front room to gather the mail as it fell through the hole to the floor. It was such a fun novelty, adding the kind of character that newer homes rarely seem to have.

It wasn’t long before the setting of my memories with my grandma took a giant detour, though. 

**************

My mom’s mascara-stained face told me everything I needed to know one morning. Even in my four-year-old brain, it was obvious that my grandma had passed away. My mom ALWAYS removed her makeup and washed her face at night, but obviously she hadn’t the night before. Sometime between when she and dad had left us kids at home with a babysitter so they could go to the hospital and when they returned home before we woke up the next morning, my mom’s beautiful mother had returned to her heavenly home. 

I will forever feel robbed that death took her away from me when I was so young. She didn’t get to physically see me become a big sister, get baptized, perform on stage dozens of times, learn to drive, graduate high school, get married in the same temple she’d been married in, graduate from college, or have my own kids. Despite her physical absence, though, Grandma Beth has stayed with me. She’s even occasionally sent me random cats to cheer me up on tough days, but that’s a story for another time.

At 67, my mom is now one year older than her mother was when she passed. And that fact terrifies me. My mom is the ONLY member of her family of origin who hasn’t had cancer. Both of her parents died of the dreaded disease—Grandma Beth from melanoma and Grandpa Conrad from bladder cancer. My mom’s older brother, Robert, was diagnosed with Hodgkin’s Lymphoma as a young father, but he was able to fight it off and survive. Her older sister, Linda, fought Non-Hodgkin’s Lymphoma and then throat cancer valiantly for over a decade, but in the end, it still took her. 

Cancer has haunted the people my mom loves for half a century. Through it all, she’s been a selfless caretaker. As my grandma battled cancer, my mom loaded me up in the car, and we went to help at her home or the hospital. We visited her at the Logan Regional Hospital often enough that I had a favorite oncologist. He wore flamboyant ties, and he always had a sucker or two ready to give me. When my mom’s dad got cancer about eight years after my grandma died, my mom helped take care of him. One would think that losing both parents to cancer long before you turned 50 AND watching both of your siblings fight it would exempt you from having the disease visit again, but you’d be wrong.

A little over 21 years after her dad died, the terrible, horrible, no good, very bad cancer came for my mom’s little buddy—my own sweet Lincoln. As was her nature, my mom stepped into our home to help us the day after Link’s leukemia diagnosis. She never technically lived with us, but she basically did Monday through Thursday for all of Link’s “frontline” treatment (the first eight months of his treatment, which were rough). Sometimes she would spend night after night in our guest room, which my boys came to refer to as “Grandma’s room”. Sometimes she would drive to her real home an hour away each night just to return the next day. And each time she stepped through our front door, my boys’ faces would light up, and I would breathe a sigh of relief.

She cleaned for us. She cooked for us. She watched Logan while Josh worked and I took Lincoln to the hospital. She offered support wherever it was needed. Her presence meant that I knew Logan was still having a blast with someone he loved when I was away. It meant that our chaotic life had a less chaotic home since she helped take care of it. It meant that when I needed a nap, I could go up to my room and collapse in exhaustion while she cuddled with Lincoln. In short, she saved us. I don’t know how we would have gotten through Lincoln’s cancer journey—especially in the middle of the pandemic—without her. 

Josh and I know that not all families are so lucky. We’ve heard from other families going through childhood cancer about how they don’t have any support from family. We’ve been so blessed with support that I can hardly even comprehend that. My mind boggles at the idea of single parents who have to juggle everything completely alone. We definitely don’t take my parents’ help for granted.

I’ll never be able to pay them back for everything they’ve done for us, but I’m always going to try. Last year when we submitted Lincoln’s Make-a-Wish (MAW) application to go to Disney World and Universal Studios, we requested that my parents be able to come with us. They were key figures throughout all of Link’s 27-month treatment, and we were overjoyed when our request was granted. Our chapter of MAW doesn’t pay for additional people outside of the wish kid’s immediate family, but Josh and I had decided that we wanted to pay for my parents to come with us. 

Of course, even paying for my parents to come with us to Florida was far from a selfless act on our part. My mom is not an amusement park enthusiast. She’s not a thrill-seeker, and she doesn’t like crowds. She went as a child to Disneyland once, and she didn’t seem bothered by the fact that she’d never gone again. It doesn’t help that she gets motion sickness. She probably would have been perfectly content to never go to another amusement park again. Luckily for us, though, she always wants to soak up as much time as possible with her grandkids.

When Josh and I told my parents about Lincoln’s wish trip, both of them said it sounded amazing and they’d like to come. I think my mom mostly wanted to witness the excitement and joy on our kids’ faces. Plus, like me, she’d wanted to visit Harry Potter World since before it opened. We’re huge “Potterheads” in my family.

We thought my dad, on the other hand, would be right at home at Disney World. He loves being around people and having fun. He’s tall, loud, and has a one-of-a-kind laugh. I frequently tell people that he’s like Goofy. He brightens everyone’s day and loves doing so. In fact, he literally plays the “Jolly Old Elf” at Christmas parties every year.

Our months of waiting for the trip ended the week before this past Thanksgiving. We flew to Florida on November 17th, and we flew back home on November 22nd. Just like throughout Lincoln’s treatment, my parents were with us the whole time. It takes a village, and every village deserves a celebration after they slay a dragon together.

The fact that we were able to go on the trip and all have a great time was a miracle in and of itself. We thought we’d be safe from hurricane season going in mid-November, but we were wrong! Hurricane Nicole hit Orlando the week before our trip. We were originally supposed to go that week, but LUCKILY Make-a-Wish had to bump us to the next week. On top of that, both of our boys (especially Lincoln), were sick off and on—in and out of the hospital—for months before our trip AND months after it. Our trip fell squarely in between lots of weeks of uncertainty about whether or not we’d be able to go. Lots of people joined us praying that everything would work out. Once again, our prayers were answered, and Link’s ideal wish trip was granted.

The trip included three days at Disney World and two days at Universal Studios. We stayed at an amazing place called the Give Kids the World Village. The Village was founded by Henri Landwirth, a Holocaust survivor, and it provides weeklong, cost-free vacations for critically ill kids and their families. (I’m actually reading Landwirth’s memoir right now, and it’s fantastic!) Everything about this 89-acre place is magical: free carousel rides that my kids couldn’t get enough of, a dinosaur-themed miniature golf course, a giant train display AND an actual train to ride on, a life-sized Candy Land game, delicious meals, unlimited ice cream, and more. It was all included. We feel so blessed that we got to experience it, and we can’t wait to go back and volunteer there someday.

At Disney World, we got to watch my Star-Wars-loving parents’ faces light up as we experienced Galaxy’s Edge. We got to watch snow fall on Main Street together at Mickey’s Very Merry Christmas Party. We got to share scrumptious treats at Epcot. We rode a ton of rides and each picked out our favorites.

It was ironic, though, when our predictions of how my parents would enjoy the trip ended up being practically the opposite of what we’d expected! My dad was the one who needed to take frequent breaks, while my mom was the Energizer Bunny and kept being adorably surprised at everything Disney World had to offer. My dad got motion sickness more and chose to stay behind at our villa one day while my mom soaked in Harry Potter World at Universal Studios with us. (Though, to be fair, we suspected certain sporting events on TV prompted him to stay back just as much as anything else, sports fanatic that he is.) All in all, the six of us had a once-in-a-lifetime vacation together.

Will a free vacation pay my parents back for their priceless service to us? Unequivocally no. But we hope it showed them how much we appreciate them. And I will always cherish the memories my boys were able to make with them there.

My mom won’t be nearly as thrilled with the other “gratitude gift” I’m going to give her. I’m going to force her to schedule a routine doctor’s appointment for herself. She’s always taking care of others and putting herself last. She can’t remember the last time she went to a doctor, but I’m going to make sure that changes. As I get older and more and more of my friends lose their parents, the thought of losing mine almost sends me into a panic attack. Since early detection is the key to fighting so many diseases, I want my mom to get checked ASAP. She’s probably 100% fine! When I asked her why she hasn’t been to the doctor for so long, she said that people go to the doctor when they don’t feel good, and she’s felt perfectly fine.

Though she’d never admit it, it’s possible she’s also a bit scared of going to the doctor and being told bad news. She’s experienced enough of that with the people around her for a fear to be perfectly understandable. It’s also not like she never goes to the hospital. She frequently accompanies my dad, who had a stroke when I was in high school and miraculously recovered, to his many follow-up visits. She just doesn’t go to appointments for herself. Better the monster you can see and fight than the one lurking in the shadows, though, so she’s scheduling herself an appointment! 

As parents, we’re expected to check under our kids’ beds for monsters. Sometimes, though, kids have to do it for their parents, too. From generation to generation, the incredible moms in my family have forged strong armor together. I know we can come out victorious against anything, but I’m really hoping we just get to relax and have fun together for a long spell now. Maybe Grandma Beth can send us some cats to fend off the monsters.

Lincoln’s Make-a-Wish Trip to Orlando, Florida

Lincoln’s Make-a-Wish Trip to Orlando, Florida

We got back from Lincoln’s Make-a-Wish trip late on November 22nd, and we’re still on a high from it. The trip was amazing, and we will cherish the memories we made there forever. They automatically included so much on the wish trip. I’m blown away 

Silver Linings in a Gold Month: Blessings We’ve Received Due to Link’s Cancer Diagnosis

Silver Linings in a Gold Month: Blessings We’ve Received Due to Link’s Cancer Diagnosis

September is Childhood Cancer Awareness Month. I worked on a different blog post about childhood cancer for several weeks in September, but it was honestly really hard. I bounced around working on one blog post after another, trying to get up the motivation to complete 

Blue Skies: A Beachside Retreat for Families Living through Childhood Cancer

Blue Skies: A Beachside Retreat for Families Living through Childhood Cancer

What Vacation?!

You know the good ol’ saying, “I need a vacation from my vacation!”? Yeah. I definitely needed one after our trip to Georgia. We’ve been home for a whole month, but I came home with a horrible cold that refused to leave me alone. That combined with typical busy summer activities made settling back in take longer. I’m finally feeling rested and back to normal, though. It’s high time I tell you about our incredible time with Blue Skies on St. Simons Island!

What is Blue Skies?

The tagline for Blue Skies Ministries reads, “Imagine a world without childhood cancer. Until then… Blue Skies ®”. They offer a bright patch between the clouds for families living through the realities of childhood cancer. Just like Lighthouse Family Retreat, they provide beach camps for families.

Our whole group enjoying the pool at Neptune Park

They offer summer camps in both Florida and Georgia. This year they’re also offering a fall weekend camp in Pigeon Forge, Tennessee. We went for a weeklong summer camp to St. Simons Island, Georgia from July 10th to the 15th, and it really was one of our best weeks ever.

Trip Planning

We loved our time with Lighthouse Family Retreat last summer so much that I was REEEEAAALLY hoping we’d be able to go again this year. I applied for another retreat early on this year, but we were put on their waitlist. They have limited spots available for returning guest families, as they want every childhood cancer family to have the opportunity to go at least once. I 100% support this policy, but I was still super bummed that we didn’t automatically get in. I told several people that it was probably my own fault they didn’t have space for us since I’d trumpeted to anyone and everyone in my cancer circle how amazing LFR was and encouraged them to apply. 😂

I didn’t want to leave us being able to go on another retreat up to chance, so as soon as I found out we were on LFR’s waitlist, I started researching. I wanted to find out if there were any other similar organizations. To my delight, I found out there are several! After reading about each of the ones I found, I decided to apply to Blue Skies. It seemed to be very close in style to LFR. In fact, I later found out they were both started by the same incredible woman! (Melinda Mayton is a superwoman!!!)

I’m so glad I applied to Blue Skies and we were accepted! While we were notified a few times that there were openings at LFR retreats, it was always last-minute, and we wouldn’t have been able to swing any of the trips. In hindsight, I’m so grateful that we were led to Blue Skies so I have the opportunity of sharing another wonderful organization with you!

Our family at Village Creek Landing on our last retreat night

The Best Week Ever

With both Blue Skies and Lighthouse Family Retreat, you’re constantly hearing people say things like, “This is the best week ever” or “There’s nothing else like it”. Both statements are true. As I’ve been pouring over pictures from our trip while writing this post, I’ve gotten more and more teary-eyed. There truly are good people in the world, and we’ve met many of them on our childhood cancer family retreats.

While we’d wanted to turn our trip into another epic, cross-country road trip like we did last summer, it just wasn’t possible this year. We were able to tack on a few extra days at the beginning, though. We flew into Atlanta on July 7th. 

And might I just say…I can now officially say that I do NOT enjoy flying with kids! 😂 This was Lincoln and Logan’s first time on a plane. While they really liked a lot of it, and that was fun to witness, it was So. Much. Work. First of all, I never pack light, so we had so much luggage. It took a long time to get through security with all of Link’s medical equipment—even WITH the extra help we got from TSA Cares. Plus it felt like we were constantly telling Logan to come back to us as he hurried too far ahead. THEN we still had to keep them entertained on the actual flight! I mean…I knew it would be a lot of work, and we went prepared, but GEEZ! So stressful. Not. Fun.

ANYWAY, we got into Atlanta super late. Thanks to it taking an unimaginably long time to get our rental car (which we’d already booked in advance, btw), we didn’t get into our hotel until around 2 AM. Luckily we were able to sleep in the next morning. We then drove down to Savannah, stopping for a visit with a friend on the way. We spent two days in Savannah, and, as expected, we fell in love with it! (If you’d like more details about our time in Savannah in another post, let me know!)

On July 10th we drove from Savannah, which is only about an hour and a half away from St. Simons, and arrived at the Sea Palms Resort around 4 or 5 PM. They had signs welcoming each cancer family lining the road up to the resort. Little details like that were sprinkled throughout the whole week, making us feel like true VIPs.

Our family with the amazing Drennans (one of our Host Families)
Our family with the incredible Simmons family (another one of our Host Families)

Volunteers greeted us with smiles and abundant offers of help. The volunteers who were specifically assigned to our family (our Host Families) were so amazing right from the start!!! We were assigned ELEVEN volunteers to help us throughout the week! In reality, though, we had many more. EVERY volunteer at the retreat was so friendly and willing to chip in at the drop of a hat. We met so many wonderful people.


After we checked in (which included getting some awesome swag), our Family Hosts followed us to our room and helped us unload our car and bring everything in. They made sure we were settled nicely before giving us some time to ourselves. We were able to relax and admire our amazing digs before the festivities began that night.

The Activities

Each day was packed with fun activities. You weren’t required to go to any of them, but they all sounded so great that we only missed a few (mainly due to our boys sleeping in). Every morning started with getting together for donuts, bagels, and drinks. As you can imagine, our sweet tooth boy (aka Logan) LOVED having permission to eat donuts every day. 😊

Yummy donuts for breakfast!

After that, Josh and I got to spend time alone with the other parents whose children were going through cancer treatments and their after-effects. Volunteers took care of all of the kids at the pool so we could just focus on ourselves. Both at LFR and Blue Skies, this time was so incredibly therapeutic and healing. It’s amazing how quickly we bonded with our shared experiences. It was truly humbling for Josh and I to share space with this unbelievable group of parents, some of whom have been fighting for and alongside their kids with cancer for close to and OVER a decade. I was always a little sad when this time together came to an end each day! 

Our days were filled with activities around St. Simons Island and Jekyll Island. We had several beach days, and, just like last year, our boys loved it. Josh and I loved it, too. Going with our volunteers may have spoiled us for all future beach days, though. 😂 They hauled all of our stuff down to the beach, set it up, took it down, and hauled it back from the beach every single time. AND everyone took turns playing with our boys and walking with Lincoln. I actually got to sit—in silence and shade —and just RELAX! 

Every night had a theme. Our first night there, we had a luau at the resort’s pool. Both of our boys got so much braver swimming on this trip! It was so fun to watch them grow up before our eyes. Swimming lessons are definitely in our plans for next year. The other theme nights included a Western Hoedown, a Parents’ Night Out (when the guest parents all went to dinner together while the volunteers took our kids to see Minions: The Rise of Gru), a Pool Party at the COOLEST waterpark on the coast, and an unforgettable Red, White, and Blue night complete with a parade, red carpet, and fireworks.

That parade, you guys… 😭 It happened on our last night there, and I don’t know if any adult was able to leave completely dry-eyed. Every time I think about it, I tear up. Blue Skies, Sea Palms Resort, and SSI collaborated to make it perfect. Volunteers decorated the resort’s golf carts, which the guest families then rode in to the gorgeous location for our last catered meal together. Policemen led the parade in their patrol cars. All along the route, SSI citizens were out on their lawns with signs and big smiles, waving to us and celebrating our warrior kids. A local high school’s cheerleading team was near the end of the route with an individual sign for each of our cancer warriors. We’ll never, ever forget it.

The Food

We ate so much delicious food while there. Blue Skies outdid themselves with their catered food selections, and we “found” a few gems (via blogs I’d read in advance) on our own. I’ll be posting a separate blog post a bit later detailing all of the scrumptious delights we enjoyed. Stay tuned!

The Worship

Just like LFR, Blue Skies is a non-denominational faith-based non-profit. Its goal is not only to provide respite for families, but also to help them feel God’s love and goodness. They do a phenomenal job of achieving these goals.

Each morning there was a worship service with a lesson taught by that week’s wonderful volunteer camp pastor. We were also unbelievably blessed to have Tasha Layton, a top Christian artist who appeared on American Idol AND was one of Katy Perry’s backup singers, perform and lead us in worship services throughout the week. I can’t even tell you how many times her amazing voice gave me goosebumps. Her personal stories inspired us all, and she was the kindest, most down-to-earth soul. Logan had fun playing with her son, so I spent a fairly good amount of time with her, and it was such a privilege.

“See ya laters”

At both LFR and Blue Skies, they don’t believe in saying goodbye. Instead, as we parted ways, our words were full of “See ya laters”. Our volunteers helped us load our car up and buckle Lincoln and Logan in. We cried tears of gratitude together as we hugged and promised to stay in touch. 

It’s hard to put into words just how special this week was, but I’ll give it a try…  

This amazing organization gave us a family vacation where we were able to relax and have fun together without having to worry about money or whether or not Lincoln would be able to participate in activities. It gave Josh and I time alone together when we were 100% confident that our boys were being cared for in our absence. It provided us with front-row seats to witness our Heavenly Father’s love for us and for others. It introduced us to kindred spirits we laughed, cried, played, ate, and sang with—people we now consider family.

If you are a family dealing with pediatric cancer, please consider applying to Blue Skies! You won’t regret it. If you know a family who’s living through childhood cancer, please let them know about Blue Skies. If you’re looking for a sensational non-profit organization to support, please consider donating to and/or volunteering with Blue Skies. I know we will be.

https://www.blueskiesministries.org/

Lighthouse Family Retreat: A Beachside Retreat for Families Living through Childhood Cancer

Lighthouse Family Retreat: A Beachside Retreat for Families Living through Childhood Cancer

July—Our Month for Childhood Cancer Family Retreats  This week we’re attending a weeklong retreat for families living through childhood cancer on St. Simons Island, Georgia. Blue Skies Ministries (BSM) is the nonprofit organization putting us up at the beautiful Sea Palms Resort. It’s been an