Tuesday, May 15, 2012
Subscribe to:
Post Comments (Atom)
This is an ongoing story of our family as we struggle day to day. Marky has a very rare disease called retro-peritoneal fibrosis which simply means there's a fibrous coating of crud all over his organs. His prognosis is unknown, since the disease is so rare. We appreciate all who visit Marky's blog and thank you for your love and support.
6 comments:
What a sweet family. I have been wanting to tell you how much your testimony meant to me. My daughter and son-in-law had a baby born two weeks ago with downs syndrome. They feel so blessed and we just love this little guy so much. Your testimony was just what I needed. (Even though I was an emotional wreck after). Thanks again.
Debbie Dazley
Beautiful family. So much happiness it shows!
Hi Debbie, Thanks for the sweet words. Im SOOOO happy for your family to welcome such a special angel into your world! These little ones bring a spirit like no other. I thought the "veil was thin" when my first child was born, and then also with my 2nd.
THEN SAM CAME ! Hard to express the beautiful gifts that accompany these special needs angels! I just shake my head, daily, with gratitude and wonder at my great fortune !
Love, Lynette
What darling pictures Lynette! Your boys are all so handsome, what a lucky momma you are! Hope you had a Happy Mother's Day!!
What beautiful family you have. I hope to one day be able to meet them in person.
Ahh, these pics turned out so great! What a treasure and what special people you all are! Love you!!!
Post a Comment