Thank you for creating this blog. Every day as soon as I can get to a computer, I log on to see how Gabriel is doing. You all are in our thoughts and prayers daily. Stay strong and take care of yourslves too.
We continue to check on Gabriel's updates daily and continue our prayers. Thank you for keeping us so informed on his progress and the pictures are great!
Peggy,Josh - it was great to see you having a good time at the zoo!! Laughter is wonderful - have some as often as you can. Gabriel sounds like he's handling things pretty well! Glad he's a strong little man. Looking forward to the next blog. Love from all in clinic- As ever, In prayer- Sylvia
This blog page was created to keep our friends and family updated on Gabriel Timothy Wittmer, born May 24, 2007 with a rare congenital diaphragmatic hernia - referred to as a Morgagni's hernia. Our many ups and downs are chronicled here to share with those who care so much about us.
3 comments:
Thank you for creating this blog. Every day as soon as I can get to a computer, I log on to see how Gabriel is doing. You all are in our thoughts and prayers daily. Stay strong and take care of yourslves too.
Hugs,
Pat
We continue to check on Gabriel's updates daily and continue our prayers. Thank you for keeping us so informed on his progress and the pictures are great!
Peggy,Josh - it was great to see you having a good time at the zoo!!
Laughter is wonderful - have some as often as you can. Gabriel sounds like he's handling things pretty well! Glad he's a strong little man. Looking forward to the next blog. Love from all in clinic- As ever, In prayer- Sylvia
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