George Charles Garman 09/09/09 to 01/29/10

January 29, 2010 our world was turned upside down when our 4 month old little boy earned his wings after a battle with Mitochondrial Disease and awoke in the Lords loving arms.

"Life can not be measured by the number of breaths you take, but by the moments that take your breath away."

George's Guardian's of Grace Projects

Stocking project is now in full force collecting donations. We have a list of the items we can use. You can also choose to sponsor a stocking in memory or honor of someone else. We will include a paragraph or two in the cards we place in the stockings to let the recipient know about the person that means so much to you. Our paypal account is posted on this page and ready to take donations. Email us for a list of items needed or with any questions or information you would like included on a sponsored stocking/donation.

Monday, September 20, 2010

Baby of the Week

I entered George's famous picture into the Baby of the Week contest that Virtua has online through Facebook. He won! God do I miss him and his precious personality. I wish he was here to do all those things that kids his age are suppose to be doing. He has been on my mind so often these past few weeks and a lot today. I miss just holding him and hugging him on a bad day...all the bad stuff would just drift away and somehow he made it all better. Now the thought of holding him just brings this whole set of pain and feelings along with aching arms yearning to hold him again.

This week happens to be Mitochondrial Disease Awareness week. Hugh, the boys, and I are all walking in honor and memory of the boys. Although I know in my heart that George had this disease, I wish that there was someway to truly know. It sounds odd but when you have no answers as to why your child died and they leave so suddenly and unexpectedly it is very hard to live with. Many doctors have told me that they feel he had it and that it was likely the reason he died but I will never really know and that is such a hard thing for anyone. Even if he didn't die from it, I do know he did have it and was my most affected child. You would never know by looking at him since he was just perfect. Those big blue eyes and huge smile and infectious laugh were always deceiving to everyone. It is such a shame that this is how it is for most of those who have this disease.

Please consider walking with us this weekend or supporting our team...Mito Monkeys

Also take the time to educate yourself about the disease, you cant tell someone has it just by looking at them. There are so many people who have this that don't even know it. For more information visit:

Help give families the hope of a someday finding treatment or a cure!

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Video Tributes/Celebration of Life Footage

Here is a link to a video tribute that was made by Richard's dad in memory of George. Get out your tissues!!/video/video.php?v=1360981185308&ref=mf

We Finally have footage from the service up and running:!/video/video.php?v=1368692138077&ref=mf!/video/video.php?v=1368733099101!/video/video.php?v=1368770540037

It is in 4 sections running about 17 mins each. If you were unable to attend, you can now see what you missed. We were so blessed to have everyone there with us in person and in spirit!

Me With My Prince Charming In Front of the Castle

Me With My Prince Charming In Front of the Castle