Our son Wil, whom we love with all of our hearts, born with birth defects (OECIS complex) that we do not see, all we see is our perfect Wil.....if you have never heard Wil's amazing story you need to go to May 2006 and start from 1)the beginning and just keep on reading. Enjoy!
Wednesday, May 31, 2006
Thank You
Thank You
To all of you who supported our family during that first year with Wil. Your prayers, words of encouragement, gifts, and friendship were needed and will never be forgotton.
I have a scrapbook that is filled with cards and letters from people who live all over the country, some are from people that I have never met. So many lives were impacted by Wil, it was amazing. Every once in awhile I will look thru the scrapbook and can still be encouraged by the words that were written for me and my family. This entire blog is dedicated to all of those who took an interest in my family's life. Those of you who still inquire how 'Baby Wil' is doing and to those of you who still pray for his healing and wholeness. Thank you for your perserverance and dedication.
The Wigge Family
Subscribe to:
Post Comments (Atom)
1 comment:
Sara and family,
Your families story really pulls at the heart strings! I can just emagine your trials and tiumphs! Reading your blog, i understand that you have heard from others that God only gives you what you can handle, but I so know how you feel, being a desert storm vet with MS and having a adopted child, that one day may not have her mommy... At times it is hard to have faith, but we still try and believe, and go on! The boys are so cute! And I hope you and your family join us for our 2457 VFW Christmas party this coming weekend! The little girl with the elf ears is mine! Hang in there!! And hope to see you soon! Kelly
kscolar@juno.com
Post a Comment