Comments on: VIDEO:A LETTER FROM ACTOR BORIS KODJOE AND NICOLE PARKER

By: kelly

kelly — Mon, 27 Apr 2009 19:13:09 +0000

so sad, this is a beautiful family and i send them my love from the uk, i am just so pleased to see that in spite of everything they seem so strong as a unit and the love they have for each other and the kid is so evident…

i wish them all the best..

sophie is too gorgeous lol she looks like her mama!! x

By: Trista Stockton

Trista Stockton — Thu, 02 Apr 2009 15:14:24 +0000

I’m glad im not the only one going through this. My case is a little different but same case. I have a daughter that was born in 1999 and she was born with spina bifida. We have been blessed that my daughter can walk with the assistance of k’afo’s and afo’s. She has had plenty of surgeries, including a uterial reimplant. She is going to be 10 in May and she self-catheterizes, learning after only a week. She is only on 2 every day meds now. She isn’t shy to explain to people her condition.She knows that shes a little different than other kids but we are fortunate that her school has an atomosphere that lets the kids with disabilities interact with the able-bodied kids. The kids don’t see the disability they see the kid for the kid. That is so hard to find these days and it helps with my childs confidence alot. Thank you for sharing your story.

By: Yvonne

Yvonne — Sun, 12 Oct 2008 17:59:05 +0000

My heart also goes out to them too, knowing what I had to go through when I was a child living with spina bifida. Now, I am a young adult living with it. Its not as bad as you may think. Its actually a blessing! The main thing that I have problems with is my bladder and bowels. I sometimes catch Urinary Tract infections due to catherization, which are no joke! But through everything, God has been good to me. I’m sure Sophie will be just fine! I wish there was something I could do to help. I would love to donate my time and energy for raising money and awareness about spina bifida!

By: Georgia

Georgia — Mon, 01 Sep 2008 22:30:36 +0000

Thats so sad to hear, I have to admit that I don’t know alot about Spina Bifida. But it breaks my heart to see children born with different birth defects. Sophie is an angel, she’s a beautiful little girl. I know she’s going to be just fine. I’m praying for the entire family.

By: KEEYSHAJ50

KEEYSHAJ50 — Sat, 30 Aug 2008 06:12:47 +0000

AWWW GOD BLESS THEM

By: Shirleye Jamerson

Shirleye Jamerson — Mon, 25 Aug 2008 04:05:57 +0000

Sorry!

I misspelled Nicole’s name

By: Shirleye Jamerson

Shirleye Jamerson — Mon, 25 Aug 2008 04:04:31 +0000

Dear Nicoel & Boris,

My thoughts and prayers are with you and your family.

Please know that there are so many of us out here that are walking with you in your despair and hoping for a solution asap.

I am a huge fan of the both of you.

You have two gorgeous little girls.

May God bless!
you in your despair

By: Katy

Katy — Sun, 24 Aug 2008 21:09:28 +0000

I am so sorry to hear about that. My prayers go out to you and your beautiful family.

By: Monica

Monica — Sun, 24 Aug 2008 17:56:45 +0000

I’m sorry to hear that, Carolyn, but I’m happy for your 5-year-old blessing.

By: Taylor-Symonne

Taylor-Symonne — Sun, 24 Aug 2008 13:06:45 +0000

I FEEL SO BAD 4 DEM BUT GOD WILL CUM THRU WITA BLESSING. BUT ON DA PLUS SYDE DA KIDZ R ADORABLE!!!