Somewhere in a hospital out in Seattle is a wonderful friend of mine , his name is Christopher Houser, and he is awaiting a donor for a much needed double lung transplant. Chris was born with Cystic Fibrosis. This young man has a wife Mindy and his little boy Robert waiting for him to come home to Montana one day. The wait has been a really long one now and many of us who are friends of Chris have concerns as might be expected.
I post this message here because I would like to encourage those of you who can to check out his website to learn more about both Cystic Fibrosis as well as an organization called C.O.T.A. This is the Children's Organ Transplant Association. Maybe you have someone in your own family now or a friend who has similar difficulties. It could be the information you learn about here may help one of them if they have a need. C.O.T.A. has assisted many in raising the money needed to help get the often life saving needs met.
Please do check out this site and see if you might be able to get the help you need for yourself or someone you know. And yes, if you can I would like to ask if you can contribute to the Christopher Houser fund that you do so. Thanks for reading this and in all sincerity may God bless you and yours always.
A friend of Chris, Greg Biggs
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