don’t forget us!
Please keep praying for Charlotte and her family. Neither Mummy nor Daddy has been given permission to bring her home, yet, so she is still in care, but doing well: next birthday she will be four!
Pray that she’ll continue to get well and strong and develop as she should, and that, in spite of all the family difficulties around her, that she would know she is very loved. Pray for her little brothers, Daniel and Davy, and for her little sister Christina. And pray for Mummy and Daddy, that they would be encouraged and given the grace to cope with all that surrounds them. And that they would be able to understand each other, and figure out, together, the best way to care for their little ones.
Charlotte is beautiful, I am so happy that she is doing well, and you are still fighting for your sweet Charlotte. I will pray for her return to you! May God bring blessings to your family!
Comment by Deedra — 7 August, 2007 @ 7:29 pm
Are her parents still separated? Has either of them been allowed to see her since February? Do they have any reports of her health?
Comment by Lydia — 11 August, 2007 @ 2:47 pm
I still pray Charlotte and her family and think of them often.
Thanks for updating us.
Comment by Jennifer — 24 August, 2007 @ 3:36 pm
I also still pray for Charlotte and her family and think of them often.
Cheryl
Comment by Cheryl — 26 August, 2007 @ 9:26 am
Hello Hannah,
Its Charlotte’s fourth birthday next week. Any news of how our miracle child is going and how her family are. They are all in my thoughts and prayers. Cheryl
Comment by Cheryl — 13 September, 2007 @ 9:07 am
Happy fourth birthday darling Charlotte. Thinking of you and your family today. Cheryl
Comment by Cheryl — 21 September, 2007 @ 9:11 am
I haven’t forgotten her either.
Comment by Lydia — 27 September, 2007 @ 1:33 am
I haven’t forgotten you. I miss all the photos and videos of Charlotte. I wonder how big she is now. From what I saw in the video of her (from a few years ago), she was not a vegetable but a child interested and interacting with her surroundings. In a country like the US or Canada, she’d probabaly be recieving special education and early intervention services. Often switchs (buttons that activate toys or speak) are used with children like Charlotte for play and communication. Even if she never walks or talks, she could still live a happy life in a world adapted for her. I would not prolong treatment for a child that is terminally ill and suffering (i.e. terminal cancer). but Charlotte is neither terminally ill nor suffering. She is just developmentally delayed and requires supports for feeding and oxygen. I hope she gets to go back with her family.
Comment by Laura — 3 October, 2007 @ 4:42 am
I just found this website.
Touching, so touching. She’s your own child, she should have a right to the person who brought her to this world.
I am disabled myself, not severly I’ll admit, and grew up with Aspbergers. I do find myself battling day to day with contant pains and fainting, for a disease that was never diagnosed when I was younger and I’ve had all my life, no one believed me and all my tests showed up nothing.
So I know some of the pain, not all, for she surely must have a lot more– but she is still worth prayers for the little angel she is, for the gift of Life she has been granted and may hope it is never taken away, for she has deserved it and proved she is meant to be in it.
Bless her delicate soul, may a good life be ahead of her.
Comment by Morning Star — 10 October, 2007 @ 7:42 am
Happy 4th Birthday, Chunkybutt! Jacque loves you!
Comment by Jacqueline — 22 October, 2007 @ 5:18 pm