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Emily's Intro...
Wow! Here we are in the midst of the "holiday" season; I knew it would sneak up on me! As Sarah told me today, "Only 12 more days until Christmas."
As I sit down to reflect, this year's St. Jude Memphis Marathon Weekend is prominent in my mind. I know most of you are aware Team Smiles For Sophie Forever made the trip to Memphis again, Nov. 30-Dec. 2. (See more about our team in related article.) What a weekend it was! We had a great team this year. My Dad joined in the fun, so instead of my parents spending their anniversary in Petosky as they usually do, they spent it with us, in Memphis. I am pretty proud of them, and grateful for their support. I hope I am able to complete a 5K when I am 66!
St. Jude Heroes (people who commit to trying to raise funds for the hospital) are invited to a pasta dinner the night before the race if they raise a minimum of $500. In addition to the great food, participants are thanked, recognized, congratulated and inspired through the words of the ALSAC president and a St. Jude patient/family. Many laughs and lots of tears are shed. People who are attending the weekend for the first time are given a glimpse of what an amazing place St. Jude is, and why their support is so crucial. Of course I am biased, and I know first-hand what St. Jude has to offer, but for many people (as it was for me before February 2007), St. Jude is a faraway place you hear about on radiothons and TV "infomercials." I honestly feel that participating in the weekend is a life-changing experience, and being a "hero" makes you realize that the running and training really isn't about you, it's about the kids. This year, I completed my first marathon - something I never thought I would want to do. Throughout the training, I told myself that this was a one-time deal. But here I am, two weeks later, seriously contemplating doing the full again next year!
It's always an amazing experience regardless of the race you complete, but for some reason, I really felt like committing to the training and finishing the 26.2 miles brought me closer to understanding the battles that the St. Jude patients (and all kids with cancer) face every day. I can't say enough how inspiring the whole race is. There are so many examples. Ask anyone on my team! During her run, my sister watched a wheel chair participant take a major spill on a downhill. She witnessed other runners coming to his aid and helping him repair the wheel and patch up his road rash. I saw St. Jude marathon runners often stop and clap for the bands and musicians playing on the streets. I saw many people cheering on fellow runners and helping them through the tough moments. With 17,000 runners, the streets were often crowded. Accidentally bumping shoulders with a runner next to you, didn't bring an annoyed look, only a smile and an "I'm sorrry." My friends Kathy and Jennifer said they couldn't fight back the tears running through the St. Jude campus as the doctors, nurses and patients cheered them on, holding signs that read, "Thank you for saving my life," and "You are MY hero." Kathy said the tears flowed again while hearing the song "Held" by Natalie Grant stream through Pandora near the end of the race as it inspired her to finish the 26.2 miles.
There are so many stories of inspiration I could share, but even typing them on a computer can't begin to do the event justice. Many have asked me how the race was, and I repeat most of the same memories. (Thank you for asking by the way!) Sharing one's personal "story" of running a marathon reminds me a little of sharing the details of your wedding, pregnancy or giving birth. Each story is different, and people like to talk about it. I will give you a little synopsis. Was it hard? Yes. Impossible? No. Memphis has a lot more hills than Cleveland, and the temperature climbed to almost 70 degrees with pretty steady winds, which never seemed to be at my back! How long did it take me? About 4:49 minutes. ( I never claimed to be fast!) Yes, there were many times when I walked. Everyone who told me it would be more mentally than physically tough was so right. At mile 12, when the runners completing the half marathon went one direction, and I had to go the other and complete 14 more miles, I seriously reconsidered the full. Not because I was so tired, or in so much pain, but just because I knew it wouldn't be easy. And I just wanted to be done. Miles 13-16 were the hardest for me mentally. At mile 13.5 my ankle was feeling a little sore and I was afraid I was going to get stuck out at mile 18 and not be able to walk. For the first time that race, I prayed to Sophie for two things. For one, to take the ankle pain away and two, to help me get focused. I swear, the remaining 10 miles really weren't so bad once I said that prayer! I started thinking about all the times that Sophie probably "just wanted to be done" with cancer and radiation; but she didn't have that luxury. I thought about all the kids and families being treated at St. Jude who would probably give anything to only have to worry about training for a marathon, instead of worrying about their child with cancer. During the second half of the race, I played "pass and get passed" with a runner with only one leg. He, Sophie, and all the kids inspired me. And then, although the remaining miles were slow, they weren't horrible. At mile 24 when I approached the hospital for the second time, I thought of the comment on the route preview blog which said, "As you make a counter clockwise loop around the St. Jude campus perimeter you can draw inspiration from the true struggles going on inside those buildings. That dose of perspective can help propel you over the last two miles." There is so much more I could say about the race, but I have already taken up more space than I am allotted! If you want more details, I am happy to share.
By race day, 7100+ St. Jude Heroes had raised $5.7 million dollars. Simply amazing yet disheartening at the same time. Why? Because it costs over $1.8 million to run the hospital for one day. As you can see the fight is not over. If you would still like to donate to our St. Jude team, you can click here to visit my personal fundraising page. I want to express my gratitude to those of you who donated in support of my efforts. I can't explain how much it means to get an email telling me I received a donation. So, I thank you from the bottom of my heart. And guess what? It's never too late for you to make a difference, and no dollar amount is too small.
As for next year, 2013 race registration opens in May, and all the races sell out pretty fast. (The half and full will sell out within the first month). If you want to make a New Year's Resolution you won't regret, commit to join team Smiles For Sophie Forever in Memphis next December. We'd love to add new heroes to our team! All are welcome, and if you decide today, you will have almost a year to train! (I'm just a wee bit inspired by the work St. Jude does, can't you tell?) Here is just a glimpse into the highlights of past years.
As we wrap up 2012, don't forget there is still time to order our 2012 SFSF Christmas ornament. This year's rendition is my favorite so far. It has an imprint of the very last rainbow Sophie ever drew (June 2007). If you would consider supporting SFSF one last time in 2012, it would mean so much to me. My good friends Jen and Lance Esparza just purchased 32 of them! 32! They are using them as gifts for family and coworkers, and giving back to SFSF in more ways than one. I thank them and everyone who has bought an ornament thus far. Maybe you might consider giving an ornament to someone who might not know about SFSF. You can click here to order one (or more!). If you live in Avon Lake, I am happy to deliver yours to you to save you shipping, and anyone local to my Mom in Michigan, can get one from her! Thanks for your support!
In closing, I would like to express my gratitude to all of our 2012 SFSF supporters. You have given us the ability to continue our mission and for that we are eternally grateful. We thank those of you who have given your time, talent, and/or treasure in ways big and small. We wish you and your families nothing but health and happiness in the New Year. And as we scurry about making last minute preparations and worrying about things that we can't control, I ask you to take a minute and reflect and give thanks for your health and the health of your kids. Because today, and every day, including Christmas, a child will be told he/she has cancer. And while each child will fight the fight of his/her life and battle with more strength than most adults, only some will be given a chance for survival, while others will hear the words of utter devastation: "terminal, and nothing we can do," facing the reality that this might be their last Christmas together. It's a wakeup call no one should have to get. I myself still wonder and wish about what things I would do differently had I known that 2006 would be Sophie's last Christmas. So I thank you today and every day for making a difference and joining in our battle to someday win the fight and prevent children and parents from facing this devastation. May you always be Held.
Warmest Wishes,
Emily Quayle
SFSF Board President
Sophie, Sarah, and Marie's Mommy
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DIPG Spotlight: Ava Dawson
Beautiful Ava Dawson, this issue's DIPG Spotlight, will be spending her Christmas in heaven this year, along with countless other DIPG victims, singing, dancing, and laughing and celebrating at Jesus' birthday party in the sky.
Diagnosed just last December, Ava earned her angel wings on November 19, 2012, less than a year after her initial physical symptoms of "hurting legs," poor balance, drooling, and trouble swallowing, as well as her emotional symptoms of temper tantrums and outbursts.
The daughter of Cindy and Jeremy Dawson, and big sister of Myla, Ava and her family are from Killeen, TX. After an MRI at Dells Children's Hospital in Austin, the family "moved" to Phoenix to partake in a clinical trial, as well as to be close to family members. The trial ibegan with six weeks of radiation, along with the chemo, Cetixumab.
While in Arizona, Ava and her family were able to attend a Ronald McDonald House luncheon planned by Grandma, raising $600 for the RMH which so graciously provided services for Ava's family during her hospitalization.
Following her radiation and her birthday party at Zoomerang, courtesy of the establishment, Ava and her family enjoyed a much-awaited and well-deserved "Make-A-Wish" trip to Disneyworld, staying at Give-the Kids-the World facility, where ice cream for breakfast was a daily ritual. Ava, full of life, enjoyed her princess lunch with Sleeping Beauty and her numerous dare devil rides on Space Mountain.
Back in Arizona for Phase Two of her protocol at the end of March, Ava began the 30-week, 3-cycle regimen of Irinotecan and Cexitumab. The second week of the cycle, the chemo was administered at a nearby clinic, allowing for more time to enjoy the warm Arizona weather.
During April, Ava began keeping a "grateful" journal provided by Children's Cancer Network, an item for which Ava's parents are now grateful. Morgan Kervin Photography also took some wonderful family photos of the Dawson family during April, capturing precious moments in Ava's life.
By May, Ava was to begin Cycle 3, but her low blood counts set her treatment back a week. When a lesion on the front of her brain, as well as tumors on her spine, was identified by an MRI, Ava was removed from the trial. Returning home to Texas, Ava was then given additional radiation on her spine and frontal lobe. Although no more radiation could be done on the pons area, doctors believed that the new tumors were caused by cells which made their way from the pons area.
Summer in Texas is hot, very hot, but by August, Ava was able to enjoy some of the outdoors. To Cindy's great dismay, there was no excitement of clothes shopping and returning to school, but Ava was able to spend precious time with her sister, laughing and giggling, enjoying each other's company. Although not in need of marrow, Ava served as the poster child for the "Be The Match" bone marrow registry, held in September, and was so excited to help other cancer victims.
Weakened by the tumors, Ava could no longer walk, but she did dress for Halloween, and her excitement was evident in the so many photos capturing her spirit. Ava also took part in The Gold Hope Project, whose mission is to bring awareness to childhood cancer through photography and the Dawsons were honored when Ava's glitter photo shoot was used when Ava was selected as a TGHP ambassador.
Laid to rest in her "perfect, pink casket," with an moving eulogy by her dad, Ava was given a final good-bye with the release of dozens of pink and purple balloons, captured in many photographs and videos.
SFSF extends heartfelt sympathies to the Dawson family, recipients of a SFSF family grant earlier this year. |
Gifts of time and love are surely the basic ingredients of a truly merry Christmas.
~ Peg Bracken |
And the winner is...
Jeff Weber of Fairview Park was the lucky winner of the SFSF Hot Air Balloon Raffle. Jeff purchased his ticket at the SFSF Golf Outing at Mallard Creek in Columbia Station back in September. Jeff's daughter Julie is married to Zach Arnold, a friend of Marc's and an avid SFSF supporter.
Jeff jokingly said, "...I'm not sure whom I'll take on the ride, but it'll probably be Christine, my wife of 45 years." Jeff, who recently retired from Parker, Hinnifin Corp after 43 years, and his wife plan on spending some time in Arizona this February; since there are over 200 locations where the ticket can be used, he's hoping that there is one over the Grand Canyon. Yes, perfectly breathtaking, Jeff. Congratulations.

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When life gives you lemons...
Although summer is long over, the rewards of summer's unseasonably warm weather plays on for Smiles For Sophie Forever. Abby Collins was a friend of Sophie's and shared hours of play group time together before Sophie's DIPG diagnosis. The daughter of former SFSF Board members Mike and Laurann Collins, Abby was eager to raise money for SFSF. She took advantage of the heat and unquenchable thirsts by selling lemonade outside her home, earmarking the profits to SFSF.
Thinking the heat would also be an attractive lure for popsicle sales, Abby added them to her stand, but unfortunately the heat took advantage of the popsicles. Laurann, recently presented SFSF Board President Emily Quayle with $2.25, the profits of the lemonade stand. SFSF is grateful for the love, concern, and generosity of the young people of Avon Lake. |
Sun shines bright on Team SFSF at St. Jude
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Team SFSF after touring St. Jude Hospital. Front row: Jennifer Slater, Sarah Smith, Susie Miklaski, Emily Quayle, Trent Wilson; Back row: Frank Miklaski, Amy Wilson, Kathy Farquhar, Elizabeth Rolinski |
For the fifth consecutive year, Team Smiles For Sophie Forever participated in the St. Jude Marathon Weekend, Nov. 30-Dec.1, 2012. This year's team was once again captained by SFSF Board President Emily Quayle. Joining her were veteran participants Susie Miklaski, Amy Wilson and Sarah Smith, as well as newcomers: Trent Wilson, Amy's husband; Frank Miklaski, Emily's dad; and high school friends, Jennifer Slater and Kathy Farquhar; and Elizabeth Rolinski, Jennifer's friend and co-worker. Completing the full marathon were Emily, Sarah, Kathy, and Trent; Amy and Jennifer ran the half; and Elizabeth, Frank and Susie did the Grizzlies 5K.
SFSF had donated $10,000 to the Team's fundraising efforts in keeping with its mission of supporting St. Jude; all members registered as St. Jude Heroes and created personal fundraising pages, raising $22,876. This year, the entire team was able to not only tour St. Jude Hospital as a group the day before the race, but was also able to run through the St. Jude Campus as part of their individual races. The weather in Memphis was fantastic, with many runners clad in shorts and tees, despite an early morning start time. Over 17,000 participants, along with thousands of their supporters, attended the event...a perfect way to begin the December holiday season...giving to, supporting, and caring about those in need of the most precious gift of all...their health. To date, the event raised over $5.7 million, with fundraising pages open until January 1, 2013. SFSF supporters may contribute to the SFSF team effort by visiting the Team SFSF fundraising page.
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Christmas is the season for kindling the fire of hospitality in the hall, the genial flame of charity in the heart.
~ Washington Irving |
Encana's "Somewhere Over the Gumbo" Team
has courage, brains, and heart
 | The Scarecrow, The Wicked Witch and The Lion AKA Charly, Dawn and Frank Miklaski. |
"Somewhere Over the Gumbo" was a pot of gumbo made by several Encana employees as they participated for the third, consecutive year in the Encana Cares Annual Charity Chili/Gumbo Cook off, held October 31, 2012, at Encana's new Plano, TX office. The event culminates the month-long Encana Cares Annual Campaign, and provides employees with not only the opportunity to win money for their favorite charities, but also to provide exposure of their favorite charities to other Encana employees.
Members of the "Somewhere Over the Gumbo" Team were: Scarecrow - Charly Miklaski, (brother of Emily Quayle, SFSF president); his wife, Wicked Witch of the West - Dawn; their 6-month-old-son, Cowardly Lion - Frank; along with Dorothy - Sandy Zdunich; Tin Man - Chris Wong; The Wizard of Oz - Chris Kightlinger; Mayor of Munchkin Land - Chris Lane; Emerald City Guard - Derek Gonsuron, and even The Yellow Brick Road - Bethiah Hall; all Encana employees. Fittingly dressed as characters from "The Wizard of Oz," the team displayed courage, brains, and heart, as they promoted their gumbo in a colorful booth, complete with a rainbow, such an appropriate idea for a SFSF fundraiser. Although neither the team's chili, nor its display won a top $1000 prize, SFSF did receive a $100 donation given to each of 12 teams entering the competition. Since the event was held on Halloween, all team members were set with the costumes for the year, even Little Frank, not cowardly at all, in his lion costume made by his mom, Dawn.
The Encana Cares Annual Campaign, which runs every Oct 1-31, not only encourages employees to support their favorite charities, but also provides them with a convenient and confidential way to plan their annual charitable giving. Obviously Charly and Dawn's participation in the cook off over the years has had an effect on Encana employees. Just this month SFSF received a $7000 check from Encana, representing employee contributions and Encana's dollar-for-dollar matching program of up to $25,000 per employee, per year. Encana proudly acknowledges an 83% rate for employee participation in this year's Encana Cares Annual Campaign.
SFSF thanks Encana, their employees, and especially the "Somewhere Over the Gumbo" team for their donation, their efforts, and the exposure of SFSF to others.
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"Somewhere Over the Gumbo" Booth. |
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The Mayor, The Wizard of Oz and Dorothy AKA Chris Lane, Chris Kightlinger and Sandy Zdunich. |
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Dorothy and The Yellow Brick Road AKA Sandy Zdunich and Bethiah Hall. |
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SFSF grants surpass $330,000
Since September 1, 2012, the Foundation has helped 11 families and awarded $11,000 in grant money, bringing the total amount of family grants awarded to $250,878. The grand total donated by SFSF, including donations to The Cure Starts Now ($37,000) and St. Jude ($45,000), is $332,878.
Every month, the SFSF Grant Committee approves applications for financial assistance for families of children with brain cancer. The children of the families who received grants in September, October, and November 2012 are:
- Thomas, age 17 - medulloblastoma
- Sydney, age 4 - DIPG
- Amber, age 17 - glioblastoma multiforme grade IV
- Anonymous, age 9 - DIPG
- Austin, age 9 - glioblastoma multiforme grade IV
- Aubreona, age 12 - medulloblastoma
- Anonymous, age 12 - anaplastic ependymoma
- Kayden, age 5 - pilomyxoid astrocytoma
- Chloe, age 9 - optical glioma
- Gracie, age 6 - medulloblastoma
- Tyreese, age 7 - medulloblastoma
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SFSF 2012 Ornament makes a special gift
There is still time to order a 2012 SFSF commemorative ornament, a perfect and meaningful gift for everyone, especially those for whom Christmas means love, peace, joy, and good will.
Fifth in the SFSF collection, this year's ornament is a white, glossy 1½" ball with Sophie's full-color hand-drawn rainbow; it sells for $12.00 (2 for $20.00), with a $5.00 shipping charge. Ornaments are available in the SFSF Gift Store or by contacting Emily.
Sophie who loved rainbows, drew the rainbow in June of 2007 with her left hand, as her right hand began failing her. It is one of the last of Sophie's works of art and had been used on a refrigerator magnet and on Team SFSF St. Jude Marathon shirts. According to Emily, Sophie's mom, "This year's ornament is very special."
Ornaments from prior years are still available, as well as many new items in the recently updated SFSF Gift Store, with the exception of the first 2008 rainbow. |
Remember, if Christmas isn't found in your heart, you won't find it under a tree.
~ Charlotte Carpenter |
Liberty Elementary holds pumpkin auction;
no 'tricks', just 'treats' for SFSF
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Sarah Quayle with a few of the pumpkin auction entries. |
Although Christmas tree lots have taken over the pumpkin patches, the results of one special Halloween activity benefitting SFSF, certainly promotes the spirit of Christmas giving. The Fifth Annual Liberty Pumpkin Decorating Contest and Silent Auction will add $500 to SFSF coffers. Marc and Emily Quayle have been invited to accept the "giant check" at a North Ridgeville School Board meeting in January.
Held at Liberty Elementary in North Ridgeville, OH, the event challenges each class in the school to decorate a pumpkin to be offered at a silent auction fundraiser. The event, in its fifth year, is organized by teachers Heather Kama-Starr and Jennifer Eby and the Liberty Elementary Student Council. Once each class finished their pumpkins, --- there were 21 decorated pumpkins this year---
they were displayed in the school library, and were up for silent bids. The silent auction lasts one week. The highest bidder obviously wins the pumpkin, and proceeds are donated to a charity. SFSF was selected this year after Heather accidentally ran into Marc Quayle, Sophie's dad, this past summer. Heather worked with Marc in Emily's dorm at EMU, way back when, during Emily's freshman year, when she first met Marc.
Thanks to the generosity of the Phi Delta Theta Fraternity at Case Western Reserve, who donates the pumpkins, there are no overhead expenses.
SFSF thanks the efforts of Liberty Elementary and is especially grateful to Heather for her role in naming SFSF as the charity of choice this year.
According to Heather, "Our pumpkin event has become a Liberty tradition, and it is a great way for students to give back to the community. Each year the students work exceptionally hard to raise money and help out groups right here in Northeast Ohio. Helping Smiles for Sophie Forever was an honor. Here's hoping that one day in the near future families do not have to go through what Sophie and your entire family went through." |
It is the personal thoughtfulness, the warm human awareness, the reaching out of the self to one's fellow man that makes giving worthy of the Christmas spirit.
~ Isabel Currier |
Tastefully Simple fundraiser nets $200+ for SFSF

The Tastefully Simple on-line fundraiser, sponsored by the National Student Speech Language and Hearing Association (NSSLHA) at Bowling Green University during late September and early October, netted $200+ for SFSF. Although not planned, the fundraiser ended on October 6, the fifth anniversary of Sophie's passing. Organized by Bethany Karl, a former employee of The Little Gym in Avon, OH, who became very familiar with Smiles For Sophie Forever as she taught Sarah, Sophie's sister, and many of her friends, gymnastics, the event held special meaning for Bethany. Now a student at Bowling Green State University, studying communication disorders, Bethany is also fundraising chair of NSSLHA and was given the responsibility of selecting a charity to benefit from the fundraiser; she graciously chose SFSF.
SFSF thanks Bethany and Bowling Green's NSSLHA for its fundraising efforts and for spreading awareness of pediatric brain cancer.
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The young, the restless, the business-savvy
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Nicole Summerfield, Emma Ferrigni, and Bianca Henline selling their wares at the Snowflake Shop. |
BN Boutique, a business venture begun last year by 11-year-old Bianca Henline and 10-year-old Nicole Summerfield featured its creations at Avon Lake Eastview Elementary School's Snowflake Shop, Dec.4-5, in hopes of raising money for charity; this year's charity of choice is none other than Smiles For Sophie Forever. Sarah Quayle, Sophie's younger sister, is a first grader at Eastview.
Originally, the girls made and sold only pop top bracelets. This year they extended not only their line of products to include washer bracelets, stuffed snakes, and hair bows, but also enlisted the help of 11-year-old friends, Emma Ferrigini and Lindsay Yurick. What makes the business so special is that the girls make all their own wares, and that they donate profits to charity. Last year, the girls donated their profits to Blessings House of Lorain County. This is their first Snowflake Shop endeavor. Bianca's (B) and Nicole's (N) motto for their BN Boutique is "BN Cute, BN Fun, BN Sassy;" and they and their creations certainly have been cute, fun, and sassy.
BN Boutique items will be on sale at Charles Scott Salons in Westlake and Rocky River until Christmas, with hopes of additional sales and additional profits.
By all indications, BN Boutique will not fall off the fiscal cliff. Stay tuned to Smiles For the Season to find out how both the business as well as Smiles For Sophie Forever fared. SFSF thanks these young girls, and wishes them continued success.
 | BN Boutique's pop-top bracelets. |
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First Annual Ohio Golf Outing attracts
both local and out-of-state SFSF supporters
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One of the 21 foursomes who participated in the first annual OH golf outing: Eric Krieg, Corynn Krieg, Taylor Browns, Bob Browns |
The first annual SFSF Ohio Golf Outing, held on a great Saturday in September, provided the opportunity for some late-in-the-year golf for the twenty-one foursomes who participated. $6200 was raised for SFSF. Held at Mallard Creek Golf Club, rated number four among over 100 Cleveland area courses, the Columbia Station course offered an excellent venue for an excellent cause. Besides the 18 holes with cart, the outing included unlimited beverages, lunch, and dinner.
The winning team consisted of three Quayle brothers: Bob, Bill, and Rick and their friend, Norm Mulder. Highlighting the event were several contests and competitions, among them, a putting contest, "closest -to-the -pin," longest drive, a Par 3 betting hole, and a 50-50 drawing. Steve Hughes, the 50-50 winner, donated his winnings back to SFSF. Raffle items as well as SFSF store items were also available.
SFSF is grateful to all those who participated, and to Board members Mike Bova, Keith Dando, and Shawn Green, and SFSF supporters Zach Arnold, Bob Bodde, and Brittany Miller who were instrumental in the planning, organizing, and executing of this first annual event.
Stay tuned to SFSF newsletters and the SFSF website for information on the 2013 Second Annual SFSF Golf Outing. |
Mama Jo's Pie Fundraiser helps
Thanksgiving dinner hosts and SFSF
Serving pies for Thanksgiving dinner dessert was a little easier again this year thanks to the SFSF Mama Jo's pie fundraiser. The pies, available in 18 varieties, ranged between $9.75 and $11.00. The sale of 60 pies netted $240 for SFSF coffers. Pies were available for pick-up on the Tuesday before Thanksgiving at Pembroke School, insuring freshness and still allowing time for day-before, at-home preparations.
SFSF Board President Emily Quayle and Board Treasurer Andrea Bucci worked the distribution; SFSF thanks all who ordered pies, handled and secured the orders, and especially Pembroke School for offering not only the pick-up site but for also advertising and promoting the sale among Pembroke parents. |
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~~~ Heartfelt Sympathies ~~~
SFSF extends sincere sympathy to the family of Alivia Gibson. Four-year-old Alivia, who was the Spotlight in the fall issue of Smiles For the Season, passed away on Nov. 4, 2012. May her family and friends find comfort in knowing that Alivia is at peace, cancer-free, drawing and coloring in her new heavenly home. |
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