Wednesday, April 14, 2010

4/14 1:15pm The hospital had Kay Quinn from News Channel 5, KSDK.com, a NBC affiliate, to come and interview Megan about her wait for a heart. We are praying that God will use the story, as He did with Channel 4, to not only encourage people to become donors, but also share our faith in Christ. Be watching tonight at 5, 6, and maybe 10.

9 comments:

  1. Wayne, I just heard about Megan yesterday (my nephew's wife works for Terry Houchin and told me about it). I am fervently praying for Megan and your family!
    Kandi Tumlinson

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  2. Debbie McGuire (Hitt) and I have been friends since we were children and she told me about Megan. I have already prayed for her and will continue to do so. I've also sent this link to everyone I know - together we will have hundreds (if not more) people praying for her and I believe God will work a miracle, as we all know he can. God Bless you all

    Lisa Oliver and family

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  3. Hey Megs.....saw you on the news girlie. Even though your heart is bigger than anyone i know...you'll get one soon girl :/, love you! -abbs

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  4. Megan, my name is Abby and I just want to send my well wishes and prayers to you and your family. My mother is a nurse at Barnes CCU and since I can remember has always told myself and my brothers about her wish to be a donor and for us to decide if we want to be a donor. I saw your story on Channel 5 today and I was so impressed by your message. I can't even imagine the difficulty of your situation but while dealing with that you are on the news encouraging others to donate. Your message reached more people than you know and WILL one day save a life. Thank you for your strength and courage. You're definitely a woman to look up to. My heart will be with you and your heart this weekend.

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  5. Hi Megan. I am Kate. My son Jackson is a Heart Transplant baby. He got his heart right next door at SLCH. He was 4 pounds at transplant. He got his heart on his last day! Miracles do happen, and my little man will be 3 next month. Oh and he had Left Ventricular Cardiomyopathy with Non-Compaction. LOTS OF PRAYERS FOR YOU! I will keep checking back

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  6. Megan. My name is Mark Strout. I was diagnosed with dialated-cardiomyopathy when I was 15. I was very active in sports and actually made a Canadian ice hockey team three months before I was diagnosed. I was stable until my senior year of high school. I was put on the transplant list on April 1, 2003 and was transplanted April 23, 2003 at St. Louis Childrens Hospital. I was 18 when I was transplanted and I'm now 25 almost 26, in May. I am now doing awesome. I actually work at Barnes Jewish Hospital and would love to come and talk with you if you were up for it. My cell is 314-308-7295 or my email is mmstrout@gmail.com. Hope to hear back.

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  7. Hello Megan,

    My name is Joseph Motter and I am a frend of jenine who lives in Japn. I was wanting to pray for you directly over the phone. I am a christian and I love Jesus and I minister to the sick and they get well.

    Please contact me @ josephmotter@gmail.com

    I am waiting for your response,
    God Bless

    JOE

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  8. I have the same heart condition that Megan has. I have had it now for 9 years. I was almost placed on the heart transplant list 2 years ago when I my heart started to weaken. With lots of prayer, my heart actually improved by 15% after doctors said it could not. I'm doing things I never thought possible....like exercising every day. I'm trusting God will provide a miracle for Megan and I'm praying for her. She's an awesome young lady and her story has touched my heart in a very special way, as one heart patient with the same condition can only know. I was diagnosed at age 39 and was very near death at that time. Anyway, I just want you to know that I am praying and trusting for a miracle here. God bless you. Kim Binkley

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  9. I am so touched by ur story and I just want u and ur family to know I am keeping you in my prayers. God still does miracles everyday!!!

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