For with God nothing shall be impossible.

Luke 1:37
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For with God nothing shall be impossible.

Luke 1:37
Facebook-f
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Twitter
Youtube
  • Mail Donations to 1367 Whitewood Ave. Spring Hill, Fl. 34609
en English▼
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af Afrikaanssq Albanianam Amharicar Arabichy Armenianaz Azerbaijanieu Basquebe Belarusianbn Bengalibs Bosnianbg Bulgarianca Catalanceb Cebuanony Chichewazh-CN Chinese (Simplified)zh-TW Chinese (Traditional)co Corsicanhr Croatiancs Czechda Danishnl Dutchen Englisheo Esperantoet Estoniantl Filipinofi Finnishfr Frenchfy Frisiangl Galicianka Georgiande Germanel Greekgu Gujaratiht Haitian Creoleha Hausahaw Hawaiianiw Hebrewhi Hindihmn Hmonghu Hungarianis Icelandicig Igboid Indonesianga Irishit Italianja Japanesejw Javanesekn Kannadakk Kazakhkm Khmerko Koreanku Kurdish (Kurmanji)ky Kyrgyzlo Laola Latinlv Latvianlt Lithuanianlb Luxembourgishmk Macedonianmg Malagasyms Malayml Malayalammt Maltesemi Maorimr Marathimn Mongolianmy Myanmar (Burmese)ne Nepalino Norwegianps Pashtofa Persianpl Polishpt Portuguesepa Punjabiro Romanianru Russiansm Samoangd Scottish Gaelicsr Serbianst Sesothosn Shonasd Sindhisi Sinhalask Slovaksl Slovenianso Somalies Spanishsu Sudanesesw Swahilisv Swedishtg Tajikta Tamilte Teluguth Thaitr Turkishuk Ukrainianur Urduuz Uzbekvi Vietnamesecy Welshxh Xhosayi Yiddishyo Yorubazu Zulu
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Month: May 2021

Jett

About Jett This is our younger son, Jett. Also known as our Jettyboy! He was diagnosed in July 2020 with CHAMP1 and he truly is our Champ! This ultra rare genetic mutation causes severe speech delay and intellectual disability, but that doesn’t stop our sweet boy! He continues to persevere, always showing us that God …

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Jeffrey Jr (JJ)

About JJ Jeffrey Jr (JJ) is our oldest son and our miracle boy. “JJ” his rare neurological condition causes severe speech disorders, seizures, cyclical vomiting, and intellectual disability. Our Son is a CHAMP1ON who fought for his life the minute he was born and we have never stop fighting for him since. He shows unconditional …

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Our mission is to improve the lives of those affected by CHAMP1 disorders through clinical research, effective treatments, public awareness, early detection, family support and patient advocacy.

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