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I know all of the people on here have 'sad days'. A day when tears come easily. I am having one of those days today so I'd like to give thanks. Today is CDH awareness day so I jumped on here to catch up with the cherubs family. I remember very well how scared I was when we found out our unborn son had CDH. It saddens me to read about new families having to deal with this medical condition. And it breaks my heart to read about other parents grieving for their children who have passed ...
well I haven't updated since our appointment on the 16th of April... Gavins Trachea is just a little too small for the stent , so they want us to come back on May 1st to check again, and if his trachea is big enough they're going to go ahead and do the surgery as quickly as the next day... I have a little extra fluid due to him not being able to breathe, but my cervix looks great , so no big concerns there... also his height, and weight is at the 52 percentile so he's doing great!!!! Anyone ...
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