<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Invisible Warriors]]></title><description><![CDATA[Invisible Warriors]]></description><link>https://www.chdinvisiblewarriors.com/blog</link><generator>RSS for Node</generator><lastBuildDate>Mon, 19 Oct 2026 06:04:41 GMT</lastBuildDate><atom:link href="https://www.chdinvisiblewarriors.com/blog-feed.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[Warrior Stories ]]></title><description><![CDATA[Every child is a warrior. This is where thier stories are told. The diagnoses that changed everything. The surgeries that no parent is ever repared  for. The long hospital days, the tiny victories, the losses that never stop huring, and the moments that remind us why we keep fighting. Warrior Stories is a place for CHD families to share the real, unfiltered journeys behind the diagnosis. Because behind every statistic is a child. Behind every child is a family. And every story deserves to be...]]></description><link>https://www.chdinvisiblewarriors.com/post/warrior-stories</link><guid isPermaLink="false">6abfdd4f197e566fc16b0dac</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 02 Oct 2026 17:02:14 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_48c68213230f4c9db4044f5a4bb57248~mv2.png/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Our Mission]]></title><description><![CDATA[Every Program. Every Family. Every Fight. It all started here. Our Mission Invisible Warriors exists because one family fell through every gap the system had to offer. A missed diagnosis. A dismissed family. A child who spent her first two years fighting for her life while doctor after doctor said she was fine. We built what we needed and never had. We built it so no family ever has to go without it again. Our mission is simple. To stand with every family affected by congenital heart defects...]]></description><link>https://www.chdinvisiblewarriors.com/post/every-program-every-family-every-fight</link><guid isPermaLink="false">6ababe970ba53dcd6a334b16</guid><category><![CDATA[Mission & Why This Exists]]></category><pubDate>Tue, 29 Sep 2026 00:33:19 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_68d1d1c52e794769825ff026389afadc~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Transparency ]]></title><description><![CDATA[Your Trust, Our Commitment At Invisible Warriors, your trust drives everything we do. Every decision we make and every dollar you give is guided by a commitment to families affected by congenital heart defects. We ensure that your support is used responsiblyand transparently to create real impact. Where Your Donations Go Your contributions are allocated to programs that directly benefit CHD families and fund milestone-based research. Typical allocation includes:     •    70% to programs...]]></description><link>https://www.chdinvisiblewarriors.com/post/transparency</link><guid isPermaLink="false">6abb06a014eeeb87d4d1be05</guid><category><![CDATA[Transparency]]></category><pubDate>Tue, 29 Sep 2026 00:32:59 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_8efb03e75a10483ea9f00972177ac327~mv2.png/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Rowan ]]></title><description><![CDATA[Rowan’s journey began in the womb. At 30 weeks gestation, he was diagnosed with DORV, VSD, PFO, and malposition of the great arteries. After birth, additional complications were discovered, including pulmonary atresia. Born at 34 weeks, Rowan spent 28 days in the NICU, during which he also developed NEC of the colon due to perfusion issues.   At 1 month old, Rowan underwent a catheterization procedure to place a PDA stent, which maintains blood flow to his lungs. He is now 4 months old and...]]></description><link>https://www.chdinvisiblewarriors.com/post/rowan</link><guid isPermaLink="false">6ad20a8e5dc461311a2aad0f</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:30:12 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_c66f2acba1024d19b65c59bdcc9d79d5~mv2.jpeg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Regina]]></title><description><![CDATA[Regina was diagnosed prenatally with DiGeorge syndrome and Tetralogy of Fallot, beginning her journey as a true heart warrior before she even entered the world. Since birth, she has undergone two heart catheterizations, a major open-heart surgery, and two additional procedures — one for her throat and another for her G-tube.   Regina continues to fight for her heart and lung health, working diligently in feeding therapy to learn to swallow, and demonstrating resilience and determination every...]]></description><link>https://www.chdinvisiblewarriors.com/post/regina</link><guid isPermaLink="false">6ad20a3ac1a47497821e65a6</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:28:37 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_1b0373705abb4d70bfc8a25031ab3993~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Gracie ]]></title><description><![CDATA[Gracie was born following a healthy pregnancy, with no issues detected during scans or check-ups. Although her birth was smooth, she struggled immediately: her heart rate was low and she was blue, requiring 11 minutes of resuscitation. Once she stabilized in her parents’ arms, they thought the worst was over.   Early check-ups showed everything was fine, and the family was cleared to go home. However, subtle signs began to worry her parents: her skin was constantly mottled, her hands and arms...]]></description><link>https://www.chdinvisiblewarriors.com/post/gracie</link><guid isPermaLink="false">6ad209afe4ecf599b68d6a35</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:26:51 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_cd892872a1ef47039a08a3ed9f670f1e~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Christian Jerry ]]></title><description><![CDATA[Christian’s journey began as a miracle. After years of being told his mother wouldn’t be able to have children, his parents finally welcomed him following a positive pregnancy test. At 20 weeks gestation, concerns about his heart led to a specialist evaluation, and by 22 weeks, Christian was diagnosed with HLHS (Hypoplastic Left Heart Syndrome) and DILV.   Christian’s parents faced multiple trips to the children’s hospital — 3.5 hours away — and underwent 1–3 stress tests per week for three...]]></description><link>https://www.chdinvisiblewarriors.com/post/christian-jerry</link><guid isPermaLink="false">6ad208725dc461311a2aa91a</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:21:43 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_12faa40525fb4db9bfd850f65a9df197~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Priscilla ]]></title><description><![CDATA[Priscilla’s journey began on December 29, 2024, when she was born at 35 weeks + 1 day gestation. Though she was low birthweight for a gestational diabetic baby, a heart murmur was detected within 24 hours, prompting a cardiology evaluation and echocardiogram. She was diagnosed with a bicuspid aortic valve with moderate stenosis, which required a week-long NICU stay for monitoring.   After discharge, follow-up was scheduled for a month later. At the appointment on January 29, 2025, her...]]></description><link>https://www.chdinvisiblewarriors.com/post/priscilla</link><guid isPermaLink="false">6ad207b2c1a47497821e6120</guid><pubDate>Fri, 16 Oct 2026 11:18:54 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_2b9356649f2547f598ffe793a218cbc4~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Jace The heart of a warrior: Tiny but mighty.]]></title><description><![CDATA[Jace is a twin whose journey began before birth. At his 20-week scan, his family learned he has Isolated Dextrocardia, meaning his heart is on the right side of his chest instead of the usual left. Initially, doctors said this wouldn’t be an issue, but follow-up testing revealed additional congenital heart defects, including TAPVR to the coronary sinus and two septal defects (ASD and VSD).   Born on September 11, 2025, Jace faced immediate challenges. He was transferred via Life Flight to...]]></description><link>https://www.chdinvisiblewarriors.com/post/jace-the-heart-of-a-warrior-tiny-but-mighty</link><guid isPermaLink="false">6ad2064c0309c5e579e5c5e4</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:13:43 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_6ede2453be2949a090f3d189e8626d27~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Ariya JamesTiny but unstoppable ]]></title><description><![CDATA[Ariya is currently 16 months old and was born with HLHS (Hypoplastic Left Heart Syndrome) and severe AVS. Her life has been a series of mountains to climb, but she has faced every challenge with determination and courage.   Her journey began at just six days old with the Norwood procedure. What followed was a whirlwind of hurdles, including a Sano stent, an emergency BTT shunt after developing hypoxemia, and the terrifying complication of a blood clot. For weeks, her chest remained open as...]]></description><link>https://www.chdinvisiblewarriors.com/post/ariya-jamestiny-but-unstoppable</link><guid isPermaLink="false">6ad204d5a61d26bfec55105f</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 11:09:33 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_49379963c4b14b7188ca0a1aefbff093~mv2.jpeg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Bryson Ivann Ralston ]]></title><description><![CDATA[Bryson Ivann Ralston   In loving memory: 3.5.25 – 3.31.25   Bryson’s life, though brief, shone with incredible courage and love. Diagnosed at 20 weeks with multiple congenital heart defects — including TGA, moderate VSD, mildly hypoplastic right ventricle, and Ebstein’s Anomaly with severe leakage — Bryson began his fight long before he was born.   Born on March 5, 2025, at 2:44 AM, weighing 6 lbs 2 oz, Bryson was immediately taken to the NICU. Though his heart was sick, his presence was...]]></description><link>https://www.chdinvisiblewarriors.com/post/bryson-ivann-ralston</link><guid isPermaLink="false">6ad20447e4ecf599b68d616c</guid><category><![CDATA[Loss Stories]]></category><pubDate>Fri, 16 Oct 2026 11:03:04 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_7bb5e2f2979b4d9db580b8ccf7c886ac~mv2.jpg/v1/fit/w_947,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Mathew ]]></title><description><![CDATA[Mathew was born with cor triatriatum, a very rare congenital heart defect. While thankfully fixable, it posed serious challenges from the start.   At just three months old, Mathew faced life-threatening complications from his condition. Though he struggled through his earliest days, his spirit and courage were undeniable.   Today, at 15 months, Mathew continues to inspire his family and everyone who knows his story. His journey is a testament to the strength and resilience of all children...]]></description><link>https://www.chdinvisiblewarriors.com/post/mathew</link><guid isPermaLink="false">6ad202220309c5e579e5be14</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 16 Oct 2026 10:54:33 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_8e66f8507a964fb5abf1310d047aae58~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item><item><title><![CDATA[Ari - "Lion of God"]]></title><description><![CDATA[Ari, whose name means “Lion of God,” has already proven just how fitting that name is.   He was born on March 23, 2023, weighing 8 pounds 4 ounces. Everything seemed perfect — until just a few hours after his birth. While holding him and trying to feed him, I noticed his breathing was raspy and labored. When I brought this up, a nurse initially dismissed my concerns as normal for newborns. But as his breathing worsened, a nurse finally listened to my instincts.   What followed is a blur:...]]></description><link>https://www.chdinvisiblewarriors.com/post/ari-lion-of-god</link><guid isPermaLink="false">6ac8d7b1d3466ffa9b95b4af</guid><category><![CDATA[Warrior Stories]]></category><pubDate>Fri, 09 Oct 2026 12:03:11 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/630248_27d409afcbca4f03a443e1343417ee6f~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Laekin Weller</dc:creator></item></channel></rss>