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Johnny Walkers Heart Journey

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Johnny Walker was born on May 5, 2023 with the diagnosis of cleft lip and palate, Heterotaxy syndrome with situs inversus, normal spleen, dextrocardia, Right ventricular dominant atrioventricular septal defect Rastelli type C. Double outlet right ventricle with side-by-side great arteries (aorta to the left with moderate to severe PS and a double aortic arch creating a lower trachea vascular ring with moderate narrowing. 

Only 1 in 10,000 babies have Heterotaxy and no case is ever the same so no baby in the world will have his same diagnosis making this a very complex surgery and recovery. 

Johnny had open heart surgery 8/17/23 and as they are now set on the road of recovery he will need constant love, prayers, and support from Kaleigh & Chris (parents). Chris is temporary out of work threw this process and while financial help cannot relieve all the stress off of this family, we want to make sure that finances can be off of their minds. 

I made this GofundMe to help the family with travel, food, lost wages, medical, and all the needs baby Johnny will have to have threw this process. 

Kaleigh and Chris are asking for endless prayers for baby Johnny and appreciate all the love and support from all of you.
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    Organizer and beneficiary

    Brett Smart
    Organizer
    Dayton, TX
    Kaleigh Williams
    Beneficiary

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