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	<title>Sugar Angel &#8211; Icing Smiles, Inc.</title>
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	<title>Sugar Angel &#8211; Icing Smiles, Inc.</title>
	<link>https://www.icingsmiles.org</link>
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		<title>Belle of the B-Cell ALL</title>
		<link>https://www.icingsmiles.org/belle-of-the-b-cell-all/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=belle-of-the-b-cell-all</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 14 Jul 2023 00:00:00 +0000</pubDate>
				<category><![CDATA[Medical Families]]></category>
		<category><![CDATA[Baking A Difference]]></category>
		<category><![CDATA[cancer]]></category>
		<category><![CDATA[Icing Smiles]]></category>
		<category><![CDATA[Sugar Angel]]></category>
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					<description><![CDATA[Sweet Aubrey Jane was diagnosed with cancer at the tender age of 3, but she faces the fight with the grace of a princess; she is truly the belle of the B-Cell ALL.   Friends, family, and the community have rallied behind Aubrey in her fight against cancer. Continue reading to find out what it [&#8230;]]]></description>
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<h4><span style="font-weight: 400;">Sweet Aubrey Jane was diagnosed with cancer at the tender age of 3, but she faces the fight with the grace of a princess; she is truly the belle of the B-Cell ALL.</span></h4>
<p><span style="font-weight: 400;"><strong> </strong></span></p>
<p><span style="font-weight: 400;"><strong>Friends, family, and the community</strong> have rallied behind Aubrey in her fight against cancer. Continue reading to find out what it means to be “Aubrey Strong” and how one little princess has inspired many to find their own strength.</span></p>
<h2><b>A Painful Discovery</b></h2>
<p><span style="font-weight: 400;">When Aubrey was only 3 years old, she began to have unexplained pains in her legs and frequent fevers. After various appointments and procedures it was finally determined that her pain was the result of </span><a href="https://www.webmd.com/cancer/lymphoma/b-cell-acute-lymphoblastic-leukemia-children" target="_blank" rel="noopener"><span style="font-weight: 400;">B-cell acute lymphoblastic leukemia</span></a><span style="font-weight: 400;"> (ALL). </span></p>
<p><span style="font-weight: 400;">The news was devastating for Aubrey’s family, but they have persevered with optimism and honesty one day at a time. They have shared their journey on </span><a href="https://www.facebook.com/groups/1318167042447986/?ref=share_group_link" target="_blank" rel="noopener"><span style="font-weight: 400;">Facebook </span></a><span style="font-weight: 400;">and through this painful process have inspired and helped others going through similar circumstances.</span></p>
<h2><b>Motorcycles and Monsters </b></h2>
<p><span style="font-weight: 400;">It takes a true warrior princess to battle the monster that is cancer. Surgery and chemotherapy treatments are difficult, and although Aubrey amazes those around her with fortitude and resilience, her true strength comes from the love and support of those around her. </span></p>
<p><span style="font-weight: 400;">Strength came from their local church, where members shared videos of themselves shaving their heads to cheer up and support Aubrey when she had to shave her own. Strength came when friends organized a benefit ride and motorcyclists from the community joined together to raise funds for her treatments and show her how important every little princess is.</span></p>
<h2><b>Party for a Princess</b></h2>
<p><span style="font-weight: 400;">Aubrey continues to have treatments, but in the midst of the trials came cause for celebration. This<img fetchpriority="high" decoding="async" class="alignright size-medium wp-image-13701" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/08B5D7A3-EAB9-4558-B9D6-3B5D6685C2C7.jpeg" alt="" width="203" height="300" /> special princess had her fourth birthday. Her parents are so proud of her for being a brave little fighter. </span></p>
<p><span style="font-weight: 400;">Aubrey’s mother, Gabrielle, was so grateful for a special cake for her daughter on her birthday.</span></p>
<blockquote><p><i><span style="font-weight: 400;">It brought her a lot of joy to have a Belle themed cake for her birthday!</span></i></p></blockquote>
<p><span style="font-weight: 400;">Gabrielle was so grateful to throw a party fit for a princess with a cake that perfectly fit the theme. Aubrey has taken on cancer with strength beyond her years and has inspired others to be more “Aubrey Strong.” Her parents are so proud of her for being a brave little fighter. Click the link below to find out how you can “Receive a Smile” by requesting a cake for someone in your life like Aubrey who could use a cake for their celebration. </span></p>
<p><a href="https://www.icingsmiles.org/receive-smile/" target="_blank" rel="noopener"><img decoding="async" class="aligncenter wp-image-12975 size-large" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Receive-a-Smile.png" alt="Receive a Smile CTA" width="1024" height="341" /></a></p>
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		<title>An Under the Sea Gratitude Party</title>
		<link>https://www.icingsmiles.org/an-under-the-sea-gratitude-party/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=an-under-the-sea-gratitude-party</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 26 May 2023 00:00:00 +0000</pubDate>
				<category><![CDATA[Medical Families]]></category>
		<category><![CDATA[Sugar Angels]]></category>
		<category><![CDATA[Baking A Difference]]></category>
		<category><![CDATA[Cakes]]></category>
		<category><![CDATA[Icing Smiles]]></category>
		<category><![CDATA[Sugar Angel]]></category>
		<guid isPermaLink="false">http://pl-icing-smiles.local/an-under-the-sea-gratitude-party/</guid>

					<description><![CDATA[From being diagnosed with stage 4 cancer to celebrating her fourth birthday, McKenna is grateful for wonderful friends, family, and her Sugar Angel.   McKenna and her family were beyond grateful for the support of those around them as McKenna battled cancer at the very young age of 3 years old. After undergoing multiple surgeries [&#8230;]]]></description>
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<h4><span style="font-weight: 400;">From being diagnosed with stage 4 cancer to celebrating her fourth birthday, McKenna is grateful for wonderful friends, family, and her Sugar Angel.</span></h4>
<p><span style="font-weight: 400;"> </span></p>
<p><span style="font-weight: 400;"><strong>McKenna and her family were beyond grateful</strong> for the support of those around them as McKenna battled cancer at the very young age of 3 years old. After undergoing multiple surgeries and seven months of chemotherapy, it was time to celebrate life with a party fit for a mermaid! </span></p>
<h2><b>Life Isn’t the Bubbles</b></h2>
<p><span style="font-weight: 400;">For little McKenna, her first years of life were just like any other’s, but then on Dec. 28, 2018, her world turned upside down. Diagnosed with a stage 4 </span><a href="https://www.mayoclinic.org/diseases-conditions/wilms-tumor/symptoms-causes/syc-20352655#:~:text=Wilms%20tumor%20is%20a%20rare,older%20children%20and%20even%20adults." target="_blank" rel="noopener"><span style="font-weight: 400;">Wilm’s tumor</span></a><span style="font-weight: 400;">, her family faced a difficult journey. This cancer of the kidneys affects children typically at the tender age of 3 or 4. </span></p>
<p><span style="font-weight: 400;">Although most children with a Wilm’s tumor have the cancer localized in the kidneys, doctors discovered that the tumor had traveled to McKenna’s heart. She had open-heart surgery, her right kidney removed, and part of her liver resectioned as well.</span></p>
<h2><b>Part of that World</b></h2>
<p><span style="font-weight: 400;">Surgery and recovery were difficult and McKenna, and her parents were forced to stay at the Children’s Hospital of Philadelphia while their three older children stayed with family. Grateful for a successful surgery, McKenna then underwent seven months of chemotherapy and radiation — no easy task for anyone, but particularly hard on a 3-year-old girl. </span></p>
<p><span style="font-weight: 400;">Gratefully, the chemotherapy and radiation were also effective, and McKenna was considered in remission. She will continue to need scans every three months, but she no longer spends as much time apart of the hospital world.</span></p>
<h2><b>Where the People Are</b></h2>
<p><span style="font-weight: 400;">McKenna was never alone on her journey and was blessed by the support of her family, friends, and a wonderful Sugar Angel who created a stunning <em>Little Mermaid-</em>inspired cake for her Under the Sea gratitude party. </span></p>
<p><span style="font-weight: 400;">McKenna’s mother, Carrie, describes the cake.</span></p>
<blockquote><p><i><span style="font-weight: 400;">“It was an incredible cake. Beyond beautiful.”</span></i></p></blockquote>
<p><span style="font-weight: 400;">Surviving surgery and cancer is no easy feat, and McKenna and her family continue to live in gratitude for the help of others and the continuing research that goes into improving cancer treatments and medicine. Celebratory cakes are a sweet form of medicine. Click the link below to find out how you can Create a Smile by producing a cake as a Sugar Angel.</span></p>
<p><a href="https://www.icingsmiles.org/us-volunteer-application/"><img decoding="async" class="alignleft wp-image-13641 size-full" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Create-a-Smile-CTA.png" alt="" width="1725" height="575" /></a></p>
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		<title>Nate the Great: Small But Mighty</title>
		<link>https://www.icingsmiles.org/nate-the-great-small-but-mighty/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=nate-the-great-small-but-mighty</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 28 Apr 2023 00:00:00 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Baking A Difference]]></category>
		<category><![CDATA[Sugar Angel]]></category>
		<guid isPermaLink="false">http://pl-icing-smiles.local/nate-the-great-small-but-mighty/</guid>

					<description><![CDATA[Facing 20 surgeries in the first five years of his life, Nathaniel goes through each day with cheerfulness to spare.   Being born without abdominal muscles is no fun and games, yet Nathaniel takes on each day in a cheerful way. Continue reading to find out how small and mighty Nathaniel approaches life with fun [&#8230;]]]></description>
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<h4><span style="font-weight: 400;">Facing 20 surgeries in the first five years of his life, Nathaniel goes through each day with cheerfulness to spare.</span></h4>
<p><span style="font-weight: 400;"><strong> </strong></span></p>
<p><span style="font-weight: 400;"><strong>Being born without abdominal muscles is no fun and games</strong>, yet Nathaniel takes on each day in a cheerful way. Continue reading to find out how small and mighty Nathaniel approaches life with fun whether he is the hospital or at the bowling alley.</span></p>
<h2><b>Addressing the Issues</b></h2>
<p><span style="font-weight: 400;">Although Nathaniel would rather be getting strikes at his favorite place, the bowling alley, he often finds himself hospitalized for surgery instead. In fact, Nathaniel has had over 20 surgeries in his five years of life. He doesn’t let this get him down and will often be found smiling or making jokes despite the discomfort of his condition. </span></p>
<p><span style="font-weight: 400;">Nathaniel was born without abdominal muscles and has urinary tract malformations from a condition called </span><a href="https://www.webmd.com/children/what-is-prune-belly-syndrome" target="_blank" rel="noopener"><span style="font-weight: 400;">prune belly syndrome</span></a><span style="font-weight: 400;">. Because of this, Nathaniel has to carry catheter bags attached through his stomach. This fun-loving kid doesn’t let that get in his way. His mother says they remind her of tool bags, which is fitting for a boy who dreams of one day being a construction worker building hospitals and museums.</span><b></b></p>
<p><img loading="lazy" decoding="async" class="alignleft wp-image-13589 size-medium wpsmartcrop-image" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/thumbnail_chK-6LgA.jpg" alt="" width="240" height="300" data-smartcrop-focus="[62,54]" /></p>
<h2><b>Turkey</b></h2>
<p><span style="font-weight: 400;">In bowling, the term “turkey” refers to three strikes in a row. For Nathaniel, the term refers to his personality. His mother describes him as cheerful, resilient, and full of smiles and fun. Despite the discomfort of his catheter bags and the seemingly endless surgeries and procedures, Nathaniel continues to offer his cheesiest smile to the camera. </span></p>
<p><span style="font-weight: 400;">He is a ray of sunshine who finds ways to have fun — toys on his tray in bed, wagon rides down the hallways, and even pranks pretending to be asleep for picture updates on his Facebook page. You can follow the fun-loving antics of Nathaniel here: </span><a href="https://www.facebook.com/groups/2008572322708780/?ref=share_group_link" target="_blank" rel="noopener"><span style="font-weight: 400;">Nathaniel Veteto: Small But Mighty | Facebook</span></a><span style="font-weight: 400;">.</span></p>
<h2><b>All the Way</b></h2>
<p><span style="font-weight: 400;">Nathaniel’s fifth birthday celebration was a great joy to this family — a time to forget their challenges and enjoy delicious cake decorated in a truly fun way. Nathaniel’s future may include additional surgeries, but one thing is certain: Nate the Great will continue to face them with a spirit of fun!</span></p>
<p><span style="font-weight: 400;">Nathaniel’s mother, Hannah, describes the experience in her own words:</span></p>
<blockquote><p><i><span style="font-weight: 400;">“My son loves bowling, and having a cake that matched his interests was so amazing. He lit up and couldn’t stop smiling. Thank you, thank you! We are so appreciative!”</span></i></p></blockquote>
<p><span style="font-weight: 400;">Even mighty kids like Nathaniel need help to smile sometimes. Click the link below to find out how you can “Create a Smile” for children like Nathaniel who face challenges every day.</span></p>
<h2><b>Create a Smile </b></h2>
<p><span style="font-weight: 400;">Join us in baking a difference by creating a custom cake that provides a temporary escape from worry and creates a positive memory during a difficult time.</span></p>
<p><a href="https://www.icingsmiles.org/us-volunteer-application/" target="_blank" rel="noopener"><img loading="lazy" decoding="async" class="aligncenter wp-image-12970 size-full" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Become-a-Sugar-Angel.png" alt="Become a Sugar Angel" width="1200" height="400" /></a></p>
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		<title>Joshua Bombs Away Cancer</title>
		<link>https://www.icingsmiles.org/joshua-bombs-away-cancer/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=joshua-bombs-away-cancer</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 24 Mar 2023 00:00:00 +0000</pubDate>
				<category><![CDATA[Medical Families]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Cake For Kids With Cancer]]></category>
		<category><![CDATA[cancer survivor]]></category>
		<category><![CDATA[Fortnite Cake]]></category>
		<category><![CDATA[Sugar Angel]]></category>
		<guid isPermaLink="false">http://pl-icing-smiles.local/joshua-bombs-away-cancer/</guid>

					<description><![CDATA[Beating obstacles on and off screen, Joshua shows us that, just like his favorite Fortnite players, when you get knocked down, you get back in the game.   Within two months, the pain Joshua believed to be growing pains increased, revealing an aggressive form of bone cancer. For the tumor to be removed, Joshua’s leg [&#8230;]]]></description>
										<content:encoded><![CDATA[<h4><span style="font-weight: 400;">Beating obstacles on and off screen, Joshua shows us that, just like his favorite Fortnite players, when you get knocked down, you get back in the game. </span></h4>
<p><span style="font-weight: 400;"><strong> </strong></span></p>
<p><span style="font-weight: 400;"><strong>Within two months, the pain Joshua believed to be growing pains increased</strong>, revealing an aggressive form of bone cancer. For the tumor to be removed, Joshua’s leg did, too. Read more to find out how Joshua overcame these obstacles and got back in the game. </span></p>
<h2>Cracked</h2>
<p><span style="font-weight: 400;">In Joshua’s favorite game, Fortnite, the term “cracked” means that a player’s shield is broken. In April 2019, Joshua’s shield was broken when he went to an orthopedist with severe leg pain. What was originally believed to be growing pains turned out to be an aggressive form of bone cancer known as </span><a href="https://www.cancer.org/cancer/osteosarcoma/about/what-is-osteosarcoma.html" target="_blank" rel="noopener"><span style="font-weight: 400;">malignant osteosarcoma</span></a><span style="font-weight: 400;">. </span></p>
<p><span style="font-weight: 400;">Devastated and facing 19 rounds of chemotherapy, Joshua and his parents also had to make a very difficult decision. His cancer needed to be removed quickly and completely, but to get all of the cancer, he would lose his right leg. Joshua had always been brave, but he proved to be a true hero as he faced the loss of his leg with optimism. </span></p>
<h2>Full Send</h2>
<p><span style="font-weight: 400;">Just like in Fortnite, Joshua fought his enemy, cancer, at “full send”; he gave it 100% and charged into chemotherapy with determination. His leg was amputated above the knee in July. Joshua was determined to not let this stop him. As soon as he could, he got back to doing the things he loved: playing Fortnite, riding on four-wheelers, and swimming. </span></p>
<p><span style="font-weight: 400;">Joshua’s parents proved to be fighters as well, bringing awareness to the need for childhood cancer research and new medications and treatments. They created a Facebook page called “</span><a href="https://m.facebook.com/BombAwayCancer/" target="_blank" rel="noopener"><span style="font-weight: 400;">Bomb Away Cancer</span></a><span style="font-weight: 400;">” to help family and friends follow their journey and to encourage others struggling with similar circumstances. It documents their heroic journey at Full Send.</span></p>
<h2>Victory Royale</h2>
<p><span style="font-weight: 400;">Only eight months after first being diagnosed, Joshua rang the bell to celebrate no more chemotherapy. He took his first steps with a prosthetic leg just a few days later and was back in the game! </span></p>
<p><span style="font-weight: 400;">Joshua was able to beat the odds, and to celebrate, his parents had a victory-over-cancer party. He was surprised with a Fortnite-themed cake — a Victory Royale. The day would forever mark the perseverance and strength of this brave 9-year-old boy. </span></p>
<p><span style="font-weight: 400;">Joshua’s mother, Candice, describes the experience in her own words.</span></p>
<blockquote><p><i><span style="font-weight: 400;">“It was the perfect celebration with family and friends. His baker was magnificent, and the cake was the center of the party. Joshua continues to talk about his cake and how he has triumphed over cancer.”</span></i></p></blockquote>
<p><span style="font-weight: 400;">Help other children find joy as they, too, triumph over cancer. Donate today.</span></p>
<p><img loading="lazy" decoding="async" class="aligncenter wp-image-13420" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Donate-Today-2.png" alt="" width="1263" height="421" /></p>
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		<title>How Icing Smiles Helped Make Jaden’s Last Day on Earth a Celebration</title>
		<link>https://www.icingsmiles.org/how-icing-smiles-helped-make-jadens-last-day-on-earth-a-celebration/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=how-icing-smiles-helped-make-jadens-last-day-on-earth-a-celebration</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 17 Feb 2023 00:00:00 +0000</pubDate>
				<category><![CDATA[Medical Families]]></category>
		<category><![CDATA[Sugar Angels]]></category>
		<category><![CDATA[birthday cake]]></category>
		<category><![CDATA[Cake]]></category>
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					<description><![CDATA[Felicia Taylor knew it was going to be her son Jaden’s final birthday. But when she planned the party — complete with a 3-foot Diego cake made by Icing Smiles Sugar Angel Mike Elder — she didn’t know that it would also be Jaden’s last full day on Earth.    Jaden entered Felicia’s life through [&#8230;]]]></description>
										<content:encoded><![CDATA[<h4><span style="font-weight: 400;">Felicia Taylor knew it was going to be her son Jaden’s final birthday. But when she planned the party — complete with a 3-foot </span><em><span style="font-weight: 400;">Diego</span></em><span style="font-weight: 400;"> cake made by Icing Smiles Sugar Angel Mike Elder — she didn’t know that it would also be Jaden’s last full day on Earth. </span></h4>
<p><span style="font-weight: 400;"><strong> </strong></span></p>
<p><span style="font-weight: 400;"><strong>Jaden entered Felicia’s life through foster care.</strong> As an infant, he had suffered a traumatic brain injury. When other kids were going to Mommy and Me classes, Felicia and Jaden were going to doctor appointments. There were surgeries, medical procedures, and countless hours of physical therapy, occupational therapy, and speech therapy.</span></p>
<p><span style="font-weight: 400;">Yet Jaden was still just a kid. He loved the </span><a href="https://shawneemissionpost.com/2022/10/19/overland-park-inclusive-playground-184639/" target="_blank" rel="noopener"><span style="font-weight: 400;">large all-inclusive playground</span></a><span style="font-weight: 400;"> with ramped play structures, deck platforms for wheelchairs, a sensory tunnel, and a communication board with common words and symbols near their home in Overland Park, Kansas. He was delighted by music, especially when his mom sang him songs — “You Are My Sunshine” was his favorite — and was disappointed anytime he was told no.</span></p>
<p><span style="font-weight: 400;">Despite his wheelchair, he was an explorer. “He hated being confined,” Felicia says. His constant companion was a toy puppy he named Scout. His favorite TV show was </span><i><span style="font-weight: 400;">Go, Diego, Go</span></i><span style="font-weight: 400;">, an animated spin-off of </span><i><span style="font-weight: 400;">Dora the Explorer </span></i><span style="font-weight: 400;">that follows Dora’s cousin Diego, an 8-year-old boy whose adventures frequently involve rescuing animals and protecting their environment. And he relished the sense of freedom he felt in water. “He loved bath time, loved to swim,” Felicia says. “He was a water baby for sure.”</span></p>
<h2>Jaden’s Journey</h2>
<p><span style="font-weight: 400;"><img loading="lazy" decoding="async" class="alignright wp-image-13414 size-medium" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/image0.jpeg" alt="" width="224" height="300" /></span></p>
<p><span style="font-weight: 400;">But Felicia knew something wasn’t right. In addition to seizures, Jaden was experiencing intestinal issues. “I noticed he was having some episodes, but I didn’t know what was happening,” Felicia says. “I took him to the hospital, and we discovered that it was pain. He was just in a lot of pain. Since he was nonverbal, he couldn’t explain, ‘This hurts’ or ‘This bothers me.’”</span></p>
<p><span style="font-weight: 400;">For two years, Felicia and Jaden went back and forth between Children’s Mercy Hospital Kansas and Boston Children’s Hospital, the No. 1 hospital for children’s gastrointestinal issues. Jaden was diagnosed with gastroparesis, hyperthyroidism, and hyperalgesia, among other things, but nothing the doctors did improved his symptoms. His intestines were failing. After a fourth-month stay in Boston, Jaden was released “with the understanding that he most likely wouldn’t improve,” Felicia says. </span></p>
<p><span style="font-weight: 400;">When they returned home, 8-year-old Jaden was put on palliative care. </span></p>
<h2>Finding Icing Smiles</h2>
<div id="attachment_13416" class="wp-caption alignleft" style="width: 235px;"><img loading="lazy" decoding="async" class="wp-image-13416 size-medium" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/image1-copy.jpeg" alt="Icing Smiles Sugar Angle Mike Elder with Mom Felicia Taylor" width="225" height="300" /></p>
<p id="caption-attachment-13416" class="wp-caption-text"><em>Icing Smiles Sugar Angle Mike Elder with Jaden’s mom, Felicia Taylor</em></p>
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<p><span style="font-weight: 400;">That July, Jaden received a trip to ​​</span><a href="https://www.gktw.org/" target="_blank" rel="noopener"><span style="font-weight: 400;">Give Kids the World Village</span></a><span style="font-weight: 400;"> in Florida through Make-A-Wish. Prior to the trip, Felicia joined a couple Facebook groups to read about other families’ experiences at the nonprofit theme park for critically ill children. That’s when she learned about Icing Smiles. </span></p>
<p><span style="font-weight: 400;">Jaden was now on hospice, and Felicia knew it would be his last birthday. She wanted it to be special, and she knew what the theme of the cake should be: </span><i><span style="font-weight: 400;">Diego</span></i><span style="font-weight: 400;">. The rest, she left up to the </span><a href="https://www.icingsmiles.org/what-it-takes-to-be-a-sugar-angel" target="_blank" rel="noopener"><span style="font-weight: 400;">Sugar Angel</span></a><span style="font-weight: 400;">, Mike Elder.</span></p>
<p><span style="font-weight: 400;">Mike became a Sugar Angel in 2010 and has completed over 30 calls to action, including our </span><a href="https://www.youtube.com/watch?v=wvuvlBdStXo" target="_blank" rel="noopener"><span style="font-weight: 400;">25,000 cake</span></a><span style="font-weight: 400;">. The owner of </span><a href="https://www.instagram.com/blacksheepcustomcakes/?hl=en" target="_blank" rel="noopener"><span style="font-weight: 400;">Black Sheep Custom Cakes</span></a><span style="font-weight: 400;"> in Wellington, Missouri, Mike understands </span><a href="https://www.icingsmiles.org/why-a-simple-cake-is-such-a-big-deal/" target="_blank" rel="noopener"><span style="font-weight: 400;">the power of a cake</span></a><span style="font-weight: 400;">. “I had a lot of trauma as a child,” he says “A lot of dark stuff happened to me. Kids don’t deserve to be in these situations. It’s nice to be able to do something fun and positive and support a kid that doesn’t have a whole lot of that going on.”</span></p>
<p><span style="font-weight: 400;">When Mike’s not baking cakes for kiddos with medical conditions or their siblings, he’s baking </span><a href="https://www.instagram.com/p/B5LmIJYA4VA/?hl=en" target="_blank" rel="noopener"><span style="font-weight: 400;">8-foot-tall cakes for Gordon Ramsay</span></a><span style="font-weight: 400;"> or competing in bake-offs on TV (he’s been featured on more than 15 shows).</span></p>
<p><span style="font-weight: 400;">When the CTA came in from Felicia, he knew he wanted to go all out. “I wanted to make sure it was worthy of this boy,” Mike says. He created a 3-foot-tall sculpted vanilla-and-raspberry <em>Diego</em> cake. He was supposed to deliver the cake to Jaden’s favorite park, but the week before the birthday party, Jaden’s health started rapidly declining. He wasn’t tolerating any of his feedings, he was sleeping more and more, and when he was awake, he was in great pain. </span></p>
<p><span style="font-weight: 400;">On Friday, Sept. 7, Jaden moved to a hospice house. </span></p>
<h2>The Last Birthday</h2>
<p><span style="font-weight: 400;"><img loading="lazy" decoding="async" class="aligncenter size-full wp-image-13413" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/image2-copy.jpeg" alt="" width="2016" height="1512" /></span></p>
<p><span style="font-weight: 400;">The day of the party, Saturday, Sept. 8, was a beautiful day. The nurses at the hospice house decorated a tranquil outdoor area with Diego decorations. Jaden’s family; teachers, paraprofessionals, and schoolmates; and his health care providers were there. And when Mike showed up with the cake, everyone was in awe. </span></p>
<p><span style="font-weight: 400;">“It was overwhelming emotionally to see such a beautiful cake,” Felicia says. “This could have been a contest and Mike would have won hands down. His creative ability was just — he went above and beyond, I mean above and beyond, for my son. It was so cool.”</span></p>
<p><span style="font-weight: 400;">Although Jaden was really struggling, Felicia says there were a few beautiful moments when he would sit up, open his eyes, look around, and hold onto some of his favorite toys. “I could not have asked for a better day for him,” she says.</span></p>
<p><span style="font-weight: 400;">That night, Felicia crawled into bed with him at the hospice house. In the middle of the night, Jaden woke up, looked up at Felicia, and said, “Hey.” </span></p>
<p><span style="font-weight: 400;">“His favorite thing to say was, ‘Hey,’” Felicia says. “I don’t know if you’ve ever seen </span><i><span style="font-weight: 400;">Guardians of the Galaxy’s</span></i><span style="font-weight: 400;"> Groot. He says, ‘I am Groot.’ That was Jaden with his “Heys.” He had a “Hey” for hello. A “Hey” for goodbye. A “Hey” I’m happy. A “Hey” I’m angry. And we loved it. That was our language, full of “Heys.”</span></p>
<p><span style="font-weight: 400;">Felicia says it was a loving and tender moment just between Mom and son. “That was the point that I told him that he could let go whenever he was ready — that I would be OK and he could let go. And he did.”</span></p>
<p><span style="font-weight: 400;">Jaden passed on Sunday, Sept. 8, 2019, two days before his ninth birthday.</span></p>
<p><span style="font-weight: 400;">“It was so hard to do that because it’s out of the ordinary to lose your children,” Felicia says. “You don’t want your children to leave you, especially so permanently. So telling him that was really hard, but it felt right. Being able to tell him that he could let go and he could be free was like the ultimate moment, the ultimate test of being a mother. You know, just allowing your child to transition on, to leave you.”</span></p>
<h2>A Celebration of Life</h2>
<p><span style="font-weight: 400;"><img loading="lazy" decoding="async" class="aligncenter size-full wp-image-13417" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/image20.jpeg" alt="" width="2016" height="1512" /></span></p>
<p><span style="font-weight: 400;">Felicia never expected her child’s last day on Earth to be a celebration — but she wouldn’t have had it any other way. </span></p>
<p><span style="font-weight: 400;">“Every expectation of his future that he wouldn’t have, every memory of his past that he enjoyed — it was all wrapped up in that one day,” she says. “It meant that, regardless of circumstance, we could celebrate him. It was, in a sense, even therapeutic, just being able to acknowledge that he was a child. This wasn’t an adult who had lived a full life. This was a child, and having this amazing cake was just an honor of his childhood, of what he loved. So to have this cake that was like the final send off for him, to be able to have that day — it felt right. It felt good.”</span></p>
<p><span style="font-weight: 400;">A year later on Jaden’s birthday, Felicia and her other son, Jason, actually got to enjoy the </span><i><span style="font-weight: 400;">Diego</span></i><span style="font-weight: 400;"> cake. Felicia couldn’t bear to cut into it the previous year. After the party, a teacher and paraprofessional helped cut the cake up into smaller pieces so it could be frozen. On Sept. 10, 2020, they thawed the cake and ate it. </span></p>
<p><span style="font-weight: 400;">“If I were to have a regret — I mean, I don’t regret it, but I kind of wonder what the cake tasted like fresh because it was so good a year old,” Felicia says. “It was amazing.”</span></p>
<p><span style="font-weight: 400;">Now, every year on Jaden’s birthday, the family goes on “Jaden Adventures.” This year, they traveled to Omaha, Nebraska, to visit the Henry Doorly Zoo. “Jaden would have loved to have gone,” Felicia says.</span></p>
<p><span style="font-weight: 400;">Jaden’s brother, Jason, also received </span><a href="https://www.icingsmiles.org/why-we-serve-siblings/" target="_blank" rel="noopener"><span style="font-weight: 400;">Super Siblings cakes</span></a><span style="font-weight: 400;"> through Icing Smiles on his birthday. ​​”I really wanted to do something special for him because it was only a couple months after his brother passed away,” Felicia says. “So we went to Main Event and celebrated his birthday. The cake was absolutely awesome.”</span></p>
<p><span style="font-weight: 400;">“​​I’m so beyond thankful to Icing Smiles for such an amazing program,” she says.</span></p>
<h2>Give the Gift of Smiles</h2>
<p><span style="font-weight: 400;">As Felicia’s story attests, it is so much more than a cake. Contributions like yours help keep the smiles rolling. </span></p>
<p><a href="https://icingsmiles.networkforgood.com/projects/21489-donate-now" target="_blank" rel="noopener"><img loading="lazy" decoding="async" class="wp-image-13420 size-full alignleft" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Donate-Today-2.png" alt="" width="900" height="300" /></a></p>
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		<title>Into the Spider-Verse to Celebrate Liam Turning 10!</title>
		<link>https://www.icingsmiles.org/into-the-spider-verse-to-celebrate-liam-turning-10/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=into-the-spider-verse-to-celebrate-liam-turning-10</link>
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		<dc:creator><![CDATA[Icing Smiles]]></dc:creator>
		<pubDate>Fri, 22 Jul 2022 00:00:00 +0000</pubDate>
				<category><![CDATA[Medical Families]]></category>
		<category><![CDATA[birthday cake]]></category>
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		<category><![CDATA[Icing Smiles]]></category>
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					<description><![CDATA[Liam and his family celebrated his 10th birthday with an epic Spiderman cake. This is the first birthday party he has had since he was 6 years old, and his family wanted to be sure to make it extra special!  Liam’s Diagnosis When Liam was only 6 years old, he came down with what was [&#8230;]]]></description>
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<h3><span style="font-weight: 400;">Liam and his family celebrated his 10th birthday with an epic Spiderman cake. This is the first birthday party he has had since he was 6 years old, and his family wanted to be sure to make it extra special! </span></h3>
<h2><b><img loading="lazy" decoding="async" class="alignnone wp-image-13034" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/July-wk-4-header.png" alt="" width="1100" height="880" /></b></h2>
<h2><b>Liam’s</b> Diagnosis<b><br />
</b></h2>
<p><b>When Liam was only 6 years old, he came down with what was said to be a viral infection.</b><span style="font-weight: 400;"> Liam had a seizure and was rushed to the hospital where he was later diagnosed with encephalitis, a brain injury. The damage caused a rare type of epilepsy called LGS. Unfortunately, LGS cannot be controlled by medication, meaning Liam has seizures daily. Liam has not recovered completely; he lost his speech, is now non-verbal, and has experienced developmental regression. Although he cannot care for himself or go to his old school, his family is grateful that he is mobile and can do some things with minimal assistance. </span><b></b></p>
<p><span style="font-weight: 400;">Liam was in the hospital for his 7th birthday, and his past two birthdays were during quarantine times, which made it harder to properly celebrate. According to Liam’s family, they are grateful that this year they were “able to get together with Liam’s friends and family to celebrate him turning double digits!”</span></p>
<h2><b>The Cake</b></h2>
<p><span style="font-weight: 400;">Sugar Angel Lisa Velesbir from </span><a href="https://www.facebook.com/moorestowncupcakes/" target="_blank" rel="noopener"><span style="font-weight: 400;">Mrs. V’s Cupcakery &amp; Catering</span></a><span style="font-weight: 400;"> went </span><span style="font-weight: 400;">above and beyond expectations with this custom Spider-Man cake. She was familiar with Spider-Man, but not Miles Morales/Into the Spider-Verse. In order to get more inspiration, Sugar Angel Lisa decided to watch the movie and showed her design to her 22-year-old son for approval. All of her designs were edible, from the marshmallow web to the character portraits to the items on top of the cake. It was a huge hit among party guests, and even Spider-Man himself was impressed. Between Sugar Angel Lisa, Spider-Man, and Liam’s family, everyone made Liam’s 10th birthday extra special. </span></p>
<h2>Words from Mom</h2>
<p><span style="font-weight: 400;"><img loading="lazy" decoding="async" class="wp-image-13026 alignright" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/VideoCapture_20220323-143716.jpg" alt="" width="251" height="180" />Liam seeing the cake was a really special moment for everyone in attendance. His mom, Kristen, shared some kind words about their experience: </span></p>
<blockquote><p><span style="font-weight: 400;">“Everyone loved the Icing Smiles cake. So many people asked where we got it, and when I told them the story, they were amazed and thought it was wonderful. Lisa was very kind and excited to present the cake to Liam. Liam doesn’t always show a lot of emotions but there was a slight smile on his face when he saw his cake!”<br />
</span></p></blockquote>
<p>Help us create more smiles like Liam’s!</p>
<p><a href="https://icingsmiles.networkforgood.com/projects/56322-smile-squad" target="_blank" rel="noopener"><img loading="lazy" decoding="async" class="aligncenter wp-image-12974 size-full" src="https://www.icingsmiles.org/wp-content/uploads/2024/01/Become-a-Monthly-Donor.png" alt="" width="1200" height="400" /></a></p>
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