Bringing awareness to a very rare syndrome called Wolf-Hirschhorn. Our kids are special, unique and full of life! The real story about WHS can be found here.
Meet the Johnsons, a family with 4 amazing children, including 3 adults with #wolfhirschhornsyndrome. Thank you, Cori, for this beautiful video: https://t.co/EkpodCHHYd
So today is my son Adam's 30th birthday. A mile stone we were told he would never reach. He has proved the doctors wrong and has grown into a fine young man (well most of the time). He makes us smile with his wit and sense of humour. #wolfhirschhorn#syndrome
The coolest swing! The back unlatches and becomes a ramp, then you can roll right on. Sturdy with full swing range. Awesome brand new addition to a park in St. Charles IL - thank you @Kiwanis! 💛 #wolfhirschhorn
https://t.co/M9S7napB1a #wolfhirschhorn I’ll be running the Bracknell half marathon in memory of my brother, Rhys, who passed away in November 2019 at age 11. Please give where you can @wolf_hirschhorn
Sending love to the WHS community on #WolfHirschhorn Syndrome Day. We wear jeans today to celebrate rare genes 💙 Thrilled to also share the cover of my debut book, DANCING WITH DADDY! Elsie, the main character, has WHS. Here's more: https://t.co/6GHXBr7TqS @wolf_hirschhorn
El Día Internacional del Síndrome de #WolfHirschhorn o también llamado 4P, se celebra el #16deAbril de cada año con el fin el objetivo de visibilizar una enfermedad que afecta a un porcentaje de la población mundial y produce trastornos genéticos que inciden en su calidad de vida