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Below you’ll find all families with an active Shout Your Story campaign. Make purchases from their page to support them.

Emery

Meet Emery We call Emery our ray of sunshine. She radiates joy, is extremely determined, and spunky. She loves music, spinning, animals, and is always up for an adventure. She was born with Rubinstein-Taybi Syndrome, a rare genetic syndrome that effects every process and organ system in the body in different ways, Agenesis of the Corpus Callosum, which means the [...]

Juniper

Meet Juniper On January 25, 2020 at 6:04 am our sweet daughter Juniper (or Juni) made her entrance into this world. She had the dantiest fingers, big alert eyes, and the squishiest cheeks. Being that it was still two months before COVID shut things down, her two half-brothers were able to come and meet her at the hospital. Our blended [...]

Kinley

Meet Kinley In November of 2018, our family was surprised with the early arrival of our daughter Kinley, born at just 28 weeks gestation via emergency c-section. Due to her prematurity, Kinley spent her first 3 months of life in the NICU, receiving life-saving care while she continued to develop outside of the womb. Early on, Kinley had obvious struggles. [...]

Camila Sophia

Meet Camila Sophia Hi, we are the Barahona family from Atlanta GA. Our precious daughter is Camila Sophia. She was born with a rare disorder called CDKL5 deficiency disorder which is a rare developmental epileptic encephalopathy caused by mutations in the CDKL5 gene. This disorder can manifest in a broad range of clinical symptoms and severity. Camila started manifesting symptoms [...]

Cyrus

Meet Cyrus Cyrus’ story is a long one even though he’s not even 3 years old yet. Cyrus’ birth mom was told that her unborn son would not survive birth because his hydrocephalus was so severe. Cyrus was also diagnosed prenatally with a condition called Dandy Walker syndrome which is a malformation of the brain with the growth of a [...]

Lottie

Meet Lottie Lottie is a sweet, sassy, and silly 8 year-old little girl with a very rare genetic neuromuscular disease called TBCK syndrome. As of this year, less than 100 people in the World have this diagnosis. The disease effects all areas of her development. Currently she is non-verbal and unable to stand or walk. She is constantly in need [...]

Christian

Meet Christian Right when COVID hit the US, Christian was diagnosed with RSV and hospitalized. They noticed his poor head control and ordered an MRI and genetic testing. The MRI revealed a lack of myelin formation and genetic testing revealed he has a mutation in the TUBB4A gene. We were told the mutation was rare, was a spectrum, and there [...]

Evely

Meet Evely Evely is a sweet, loving, and silly kiddo who loves music, swings, and trampolines. Evely is completely blind and does not walk or talk. When it comes to finances, there's ALWAYS something. Medical bills, equipment, supplies etc. You can't ever really plan anything because you have to be somewhat prepared for what's next. {{ vc_btn: title=SHOP+NOW&style=flat&shape=square&color=chino&align=center&button_block=true&link=url%3A%2523shop-now%7C%7C%7C }} Connect [...]

Fletcher

Meet Fletcher Fletcher is happy, funny, and kind. He loves people, school. and making and passing out bracelets. Fletcher has complex medical needs, the most significant is that he requires a trach and ventilator to sustain him. He’s also immobile therefore he is solely dependent on his parents. So, even though Fletcher is almost 17 years old, his day-to-day life [...]

Miller

Meet Miller Miller is a resilient, joyful, and playful kiddo who loves Mickey Mouse, swimming, and snuggling. At 15 months old, Miller was diagnosed with Leigh Syndrome, a severe neurological disorder characterized by progressive loss of mental and movement abilities. Miller's body is running off less energy than it can sustain, like a house running on a 9-volt battery. There [...]


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