Journey thru the eyes of an angel

This is showing you amazing courage of my son Declan who is 6 years old and has Lissencephaly. Declan is an amazing little man who fights daily to be here , people only dream of seeing angels we are so lucky to hold one in our arms for the last 6 years xx

Category:

People & Blogs

Tags:

• Lissencephaly
• OneTrueMedia

[ckelly1804]

We were tested also honey, and we were both clear!!, in Decs case it was a one off!! In my eyes Declan was normal and i was so so glad to have in my life even if only for a short while!!, hope all goes well with results xxx

[XMUTAZIONX]

i felt very sad today, i had many and strong familiar problems, after i saw this video, i think i could stand more just if i want to. Thank you, you helped a complytely stranger to live with more happiness

[ckelly1804]

Thanks honey, im glad i could have helped in someway. Since that video was made Declan passed away on the 15th December 2008 . Take care x

[stormspinner1]

I couldn't do it, be as strong ... forgive me. :( What makes it so much harder is he's so cute - say a prayer for me.

*StormSpinner1* in Texas

[ckelly1804]

I f you love something so strong you can hsndle anything xx

[ckelly1804]

Thank you honey, both our boys are angels and i will forever thank god for giving me one to hold in my arms!!!

xxxx

[jcjazmin]

I am going thru the hardest think of any humans life. A few weeks ago one of my cousins lost her son at 6 months old. He was born with Miller Diekers Syndrome. On of our aunts had two children with this same syndrome. I knew immediatly that I had to get tested. I am 26 years I found out that maybe I would never be able to have a normal child. I got tested last Monday and I have to wait 2-3 weeks for the results waiting for them has been the hardes think in the world.

[REALTALK1NZ]

R.I.P DECLAN,NEVER FORGOTTEN

[CuteeBeauty]

I'm so sorry for your lost. I have a 9 yrs. old lissencephaly boy. Not one day that I don't think of about it. Hold on to all the love and wonderful times he was with the family. He will always be with you. You are blessed with a handsome boy!!

[absdababs]

caroline RIP i hope your okay my mum will come along i think what you say is truee because the courage of DK is onle of a kind i am very sorry

abigail watkins

magerets daughter .... i cannnot apoligies moree

[sweetpea4912]

Thank you so much for you video although I have to say it was kinda eri for me because he is the spitting image of my child. I have never heard of lissencephly until now. Mine has Microcephly, Cerebral Atrophy and Cp. I find it so heart warming to see others share there heart warming stories. God Bless