please take a moment to read my experience with muy sons craniosyntosis.

Mary - posted on 03/31/2014 ( no moms have responded yet )

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I have a 3 yr old little hoy that was diagnosed with metopic craniosyntosis un late 2013. Im a young Mother of 23 yrs i also have another little boy that is 18 months. When me and muy husband found out out our 3 yr old had craniosyntosis it has been a very difficult situation going thru all this knowing our son its going to need surgery to fix it, as a Mother its ver y hard todo know that tour son has to go thru this difficult thing, and more scary that he was diagnosed at an older age and he Asks all these questions, like momy why do i have this? I dont want surgery km scared? It breaks muy heart but i know gris has todo be done. My son has his surgery scheduled on may 6 2014 and currently our family is facing another struggle with muy husband having his hours cutt off and not having enough money todo cover expenses we need to travel 2 hrs todo the hospital where he needs todo have his surgery i begg all moms out there to please take a look AT gris page i created for him, and if you could please share! Anything you can do to do help me out jist by sharring will help! Thanks in advance and god bless you all! http://www.youcaring.com/medical-fundrai...

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