Getty Owl Foundation

Lionel’s Place

From Kate:  A few months ago at Getty’s school fall festival, I was introduced to a couple of dynamic women. Karen and Hannah were vendors at the festival and what they had to offer made my heart happy. Lionel’s Place, offered all kinds of fun pillows, prints, t-shirts, buttons, and an amazing book called The Little Lemon That Leapt. This is Lionel the lemon. Lionel travels the world meeting various friends along the way and learning what makes us different can and is wonderful.  What I appreciate most is Karen and Hannah’s passion and mission to help support positive efforts to help kids embrace weird. “We will never be able to measure how much greatness the world has missed out on because a bully shut down a child’s creativity. That is why it is our mission to bully-proof kids one at a time by teaching them that different is beautiful. When a child accepts and loves his or her own quirks, it in turn becomes easier for that child to accept and love quirks in others. Choose Weird is our mantra and way of empowering kids to own their differences in a positive and intentional way.” My perspective as a mother with a child with special considerations, I often worry whether Getty would be accepted in her environment. Would children only see differences as negatives? Would they not take the time to really see her as just one of the kids? Would they see what we see every single day? A confident, sassy, and incredibly smart young lady who embraces all that life has to offer. Well I can honestly report that ever since Getty has been enrolled in school, she has always encountered a warm smile and a kind offering of friendship. We have been overwhelmed with kindness and I can’t tell you how much it empowers Getty’s growth.  I am also aware that not all experiences are similar and I am so thankful for Karen, Hannah and Lionel’s Place for offering a positive platform to learn positive ways to embrace differences. Your efforts will continue to make an impact, that is certain.  “It is about a movement to raise a generation of children who are full of compassion and empathy, and who choose to celebrate what makes them weird.” I love this and I could not agree more.  This year for our SMA Holiday Giveaway, I wanted Lionel’s Place to participate. So for those SMA families entering our giveaway, you have a chance to also win one of their beautiful owl pillows and prints. Check it out!  I was obviously drawn to the owl prints. I am a bit partial to them for many reasons. I was also drawn to the phrase, “Fly Fearlessly”. I think all of our SMA kids fly fearlessly. Since Getty’s diagnosis, she has had to endure many challenges and without fail, she flies fearlessly into every challenge or hurtle with ease and grace. I am in awe of her daily and just so proud of her zest for life. She is a constant teacher that challenges me in so many ways.  I hope everyone reading can take a moment to check out Lionel’s Place.  For those SMA families interested in entering your child’s name into our giveaway, please CLICK HERE . Deadline for entries is December 3rd @ 6pm PT.       

SMA Holiday Giveaway 2017

From Kate:  I love this time of year for so many reasons. On a personal level I love how the seasons change here in Sacramento. Yes, I loathe the fact that winter is not kind and viruses linger everywhere and we always have to be vigilant, but it’s still pretty outside. Sometimes it is very hard to find the silver lining to our “normal” lives during the winter months, but holiday carols are nice and looking forward to Charlie Brown, The Grinch, Polar Express, and snuggling when the weather is colder sure makes for some great memories. Hopefully we will get the tree up soon to enjoy. We hope Thanksgiving was a beautiful day for everyone.  Another reason for excitement is what has now become an annual iPad giveaway for our SMA community. This year we will be giving away 10 iPads. We are just so thankful to have a platform to support SMA families. Thank you to our donors for supporting our efforts. We certainly could not do this without the confidence and support of all of you.  Technology serves many purposes for our SMA community. Technology opens the door to independence, education, communication, entertainment, and socialization. So much learning in our environment comes from experience, but for an individual with SMA, their could be some barriers that might not allow for opportunities. iPads offer a chance to explore, communicate, and have a sense of independence that they might not otherwise get.  So we want to help. I know 10 iPads might not be a lot, but we hope to always double our number from the year prior.   This year we have some really special additions to our SMA Holiday Giveaway. Here is a picture.  What’s inside our iPad Packages? 9.5 inch iPad. $50 gift card to be used for iTunes in the App Store. The two adorable owls (pillow & print) have come to us from an amazing mother/daughter organization, called Lionel’s Place. (More about them next week.) Last, a GOF reusable grocery bag. One awesome item that is not pictured comes from a local artist and GOF volunteer, Daisy Trotti. Her handmade crochet blankets are beautiful and perfect for the season.  What a great giveaway, huh!     Details for the SMA Holiday Giveaway 2017:  Getty Owl Foundation will be giving away 10 iPad Packages.  This giveaway is for people with Spinal Muscular Atrophy (SMA) only. While we are aware that many people could benefit from an iPad, Getty Owl Foundation’s primary commitment is to individuals with SMA.  *No purchase necessary.  * One entry per individual. (Duplicate entries will be void.)  *If you have any questions, please email me at hoot@gettyowl.org    How do you enter? Super easy.  Email us at hoot@gettyowl.org    Submit the following information:  Name Age Address Type Grade Please attach a picture.    Entry Deadline: Now until December 3rd @ 6pm PT   Giveaway Recipients Announced: Tuesday, December 5th @ 6pm PT

Even Amazingly Beautiful Things Come To An End

From Kate: After six incredible and memorable years, we have decided to no longer host the Getty Owl Run/Walk. While we are very sad to come to this decision, it is also for beautiful reasons as well.  We are thankful for Getty’s health and have decided in her interests, to give a back seat to fundraising and community outreach, for now. We will always help families affected by SMA, but for now an annual fundraising event will be put on hold.  Over seven years ago I sat down and brainstormed. Getty was around 8 months old at the time. Life was going a mile a minute. We were entering a new phase of this SMA journey with a g-tube placement, increased breathing treatments, and a looming winter season that had the potential to harm Getty.  There was also an overall heaviness that, at times felt suffocating. 8 months in, I was still a new mom, but I wasn’t sure what that meant anymore. I felt cheated out of my role as mom. I felt more like caretaker and first responder rather than given a chance to relish in this new position of motherhood. It was becoming very clear to me that my relationships with the regular world would just not be in the cards for me and our life. I was realizing that our lives were becoming less relatable.  Stories about suctioning, resuscitating, and fighting with doctors were our norm, and while I am sure I isolated myself, out of pure survival, I retracted from what I considered my old life and tried to find something I could do to feel like I was becoming part of the solution, rather than allow for this diagnosis to control my every breath.  I sat down and brainstormed about what we could do to make a difference in our community, and also create a place, a day, an event that could help serve several purposes. I wanted to bring the community together, raise money, and selfishly I wanted to feel whole. Out of the barrage of brainstorming blossomed the Getty Owl Run/Walk.  It would be a day for all abilities and ages to enjoy a morning to support a cause and also enjoy a day to relax and reflect. I wanted it to be fun and fulfilling.  As a runner myself, I thought, “How hard could it be to plan an annual run?” While planning for any event, a run is just logistically pretty crazy to take on.  Throughout the first year I had moments of asking myself, “What the heck did you get yourself into kid?” There was never a dull moment and while it was thrilling, adrenaline pumping, and often times frantic, what came of it was as close to my brainstorming as possible. Because of amazing friends and family, gracious sponsors, and companies willing to support us at every single turn, our 1st Annual Getty Owl Run/Walk was a success and every year after.  In the six years of our Getty Run/Walk, we welcomed an average of 900 registrants. We also had the pleasure of working with some incredible companies and organizations that also felt strongly about Getty Owl Foundation and our mission to spread SMA Awareness.  The last Sunday in February was and will always have a special place in our memories and hearts. It was always positive, it was always fulfilling, and it was a beautiful reminder of how awesome human beings are. Thank you to everyone who showed up and supported our efforts.  There was always a moment right before the Getty Owl Run/Walk that I got the opportunity to speak to the community. The night before I would run through exactly what I wanted to say. Without fail, the moment I stepped onto the platform to speak, words just came from my heart, not from my head. Every year was a breathtaking view — hundreds of people, standing, ready to run but also embrace why we were doing this event. I felt like every year, people just got it. They understood that SMA needed to go away and they were coming today to show their support in a way they knew how. While that moment was often only seconds, it always reassured me that Getty Owl Foundation was making a difference. We had purpose.  On February 26, 2017, I stepped up onto the platform and thanked our runners like I always do. I threw out a few SMA facts and talked about how Getty Owl Foundation was making a difference for children and families affected by SMA, as I always do.  Then my body went numb. It was a disorienting moment to stand in front of so many and explain that there was now a treatment for SMA and that Getty and some of her buddies would be getting the treatment in the very near future. The cheers and tears that came from the crowd was an experience I will never forget. What an amazing time we live in to be able to announce such a scientific breakthrough.  Since that day, Getty has been receiving the treatments and she is doing remarkably well. So far, no complications and so far Getty is retaining some strength that has been such an incredible blessing. We look forward to the future, her future.  As we moved into summer, it was becoming quite clear that we might have to rethink what we prioritized. With regained strength has come new considerations on therapies and other resources for Getty’s care.  Getty is now in second grade and her education is becoming far more rigorous than in years past and I wanted to make sure nothing was being compromised for her.  I sat down in the summer to prioritize other aspects of our lives and while I tried in every way to hold onto our annual Getty Owl Run/Walk, it was clear that the time to continue to put on the run would just not work. I was not going to put on the event for the sake of having it. The moment I thought the integrity of the run might be compromised, I knew it was time to walk away.  So that is where we are. What an amazing situation to be in! Getty is receiving a medical treatment to help her fight SMA, and there isn’t enough time in the day to care for her and put on the Getty Owl Run/Walk. Wow, what beautiful problem to have.   Thanks to everyone for being so kind and giving of your time. Thank you for signing up and running/walking. Thank you for helping us raise over $250,000.  All of the money raised is 100% put back into the Getty Owl Foundation. You have helped us raise funds to help grant iPads for communication/educational purposes. We have been able to purchase life saving medical equipment and supplies for families affected by SMA. Funds raised has helped us gift back-to-school bags, travel equipment, communication devices, and allows us to continue to help SMA families into the future.  Thank you! Thank you! Thank you!  If I can leave one message to everyone reading and that is, “You make a difference!” All non-profit organizations depend upon the generosity of the community to make a difference.  Many are 100% volunteer like Getty Owl Foundation. So many amazing foundations that have found a need in a particular community and work their butt off to make a difference. Please consider helping in any way you can. It could be a river clean up, an annual run, donating to a food bank, sponsoring a family for the holidays, donating used goods, etc. Please continue to support organizations that want to do good. You make a difference for so many!  While we will no longer be hosting Getty Owl Run/Walk, Getty Owl Foundation will continue to support families affected by SMA. We will continue with our mission to educate the community and advocate for families affected by SMA. We will continue to strive to help find a cure for SMA. We will keep on, keeping on until SMA is extinct.  Below are just a few of our favorite memories throughout the years of the Getty Owl Run/Walk. It was always a perfect day, it was always a day to celebrate and reflect, and it was always a day that Getty could ride like the wind in her flying stroller spaceship.  

Halloween 2017

From Kate:  We hope every one had a safe and fun Halloween. Getty decided to be Wonder Woman this year. I would argue that she IS Wonder Woman, but at least she was willing to dress up as her role, finally after 7 years on this planet.   The Saturday before Halloween, Getty was invited to a Halloween party at her friend’s house. That entire sentence just gives me the happy chills. She had a lot of fun and enjoyed her time hanging out with her friends and kids her age. It was awesome for her to be invited. This time of the year is always so sketchy. I want her to experience fun things, but the worry of fall/winter germs is looming, so sometimes I am a buzzkill and say no. BUT, this time I said yes and she had a great time and made some great memories.  Halloween was a blast. Getty got to participate with her cousins and even dad dressed up for the festivities. She said, “trick or treat” and “thank you” at every house which was awesome for many reasons. 1) We were out trick or treating in the first place. 2) Getty was healthy enough to go. 3) She loudly said, “trick or treat.” 4) She loudly said, “thank you.” 5) Girlfriend made a killing in treats.  

Thank You Dutch Bros.! Thank You Community!

From Kate:  I would like to wholeheartedly thank the Grubbs Family, Dutch Bros. Coffee, and our great Sacramento Community for helping raise $6810, in the Buck for Kids event on September 29th! It was a HUGE success and we are so thankful for all of the continued generosity of Dutch Bros. Coffee. Thank you for all that you do for local causes, such as ours. We are so humbled by your constant support and love.  Thank you to all for stopping by and purchasing a drink, or two. We are so thankful!  What I know for sure is that this holiday season we will be able to gift more iPads to deserving children and adults affected by SMA, and that makes our hearts sing!  Thank you all!