To those affected by a heart defect:

Happy 2nd Birthday, Haven!

December 11, 2008 at 9:04 pm by Mom & Dad

We can’t believe it’s been two years since we first saw your precious face… and you are still brightening our lives, strengthening our faith, and bringing smiles to our faces.  We love you and miss you!  Mommy and Daddy

Then we which are alive and remain shall be caught up together with them in the clouds, to meet the Lord in the air: and so shall we ever be with the Lord. Wherefore comfort one another with these words.   1Thes 4:17-18

Posted in Memorial | 8 Comments »

8 Responses

  1. Michelle Halcomb Says:

    Been thinking of you guys and Haven tons. Keeping you both in prayer. I come back to Haven’s site often just to see her cute face and remind myself of your strong faith and testimony for the Lord. Wishing you a Merry Christmas! Michelle

  2. Amber and Mike Says:

    Thinking and praying for you both on this day. May God continue to strengthen you!
    We love you TONS!!

    ~*McMullin Family*~

  3. Karrie Hulings Says:

    Thinking of you today and always. Love you all! Wishing your family happy holidays!
    Love, Karrie

  4. Karrie Hulings Says:

    DUH! Happy 2nd Birthday Haven! I forgot that in that last post 😛

  5. Uncle Justin Says:

    God continues to do so much by Haven’s story. Praise God!

    For a baby girl who could not speak a word her life spoke loudly to the need of God’s sufficient grace, and God was faithful.

    Her condition was familiar to many, but her story is one of a kind.

    We love you Haven.

  6. Tammy Myers Says:

    Happy 2nd Birthhday Haven!! We love you. Mommy amd Daddy spoke for us all, what a day that will be when we all meet again. We love you Jeremey and Alison and you are in our thoughts and prayers everyday. Thanks so much for contiuing to share the inspiration you three are through Haven. 🙂

  7. Cathy Baker Says:

    What a fun day it will be when you get to look into her big beautiful eyes once again…caught up in the clouds!

    Faith, Hope and Love…we need them all, don’t we!

    Thinking of you…

  8. The Altena Family Says:

    We continue to think of you and your angel may you always find comfort knowing many still care.

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This site contains the story of Haven Leigh and serves as a source of hope and encouragement to anyone who has or knows a child born with HLHS, a congenital heart defect, or other terminal illness. Here, we show the rewards of nurturing and supporting a special child while celebrating her memory by sharing her story with others.

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