Centrum Kids supplement contains Aspartame

What happens when you go and buy a multivitamin for your kid?
You trust that the manufacturers have your child's welfare at heart.
You trust that you are able to give him a little boost with regards today's lessened nutrients in foods and overloads of toxins.

Apparently you cannot just pick a bottle of the shelve. You have to read all of the small ingredients, and sometimes it is not even displayed on the box, but on the bottle.
Most of the times we don't know what we are buying. I find it very scary!

We not only have to check the medicines, but the vitamins as well!

Michelle West, mother of Caitlin, the twin who has cerebral palsy, went to buy vitamins, and was recommended Centrum Kids. She checked on the box that it did not contain Aspartame, but only saw at home that it actually does! In a children's vitamin!

She went on an email and Facebook campaign to warn other mothers, and was contacted and reimbursed by Pfizer.

But the product is still on the shelves in South Africa...

The whole story was also told in Times Live yesterday!

In the words of Michelle:

"If, as a parent, you decide that it is in your child’s best interest to still purchase this product, having all the information, with or without testing them beforehand, then that is your right. I won’t be accused of telling anyone what to do, and that is certainly not my intention.

To my knowledge, there are no documented white papers detailing the effects on children from different countries and of different races, having taken the product over an extended period of however many years and regularly tested to see the effects and their wellbeing. Until that sort of data is provided, I choose to give the product a skip. 

I must reiterate that this is not intended a smear campaign. For this reason, I have not revealed the names of the representatives I have spoken with. They are only doing their jobs.

As a mother, as a citizen and as a consumer, I stand for everyone in South Africa by documenting this.

Those little people that you’ve brought into this world are so precious. They are, quite rightly, our future. If we don’t look out for them, who will?"

               http://www.timeslive.co.za/local/2012/02/08/centrum-kids-supplement-contains-aspartame-ilive

Thanks, Michelle, for making us aware!


The Facebook link:
http://www.facebook.com/pages/The-Little-Train-That-CAN-Caitlins-Story-So-Far/170667849610462

Caitlin got her "soldiers" - stem cell therapy

Caitlin
Photo taken from The little train that can: Caitlin's story so far on FB

The story of a little girl named Caitlin has a happy endingbeginning. 

Caitlin has a wish of the use of normal arms and legs, the same as her twin sister. 

(Caitlin, I wish for you as well!)

She was diagnosed with Spastic Diplegic Cerebral Palsy, and it was the dream of her mother Michelle even before she could comprehend it herself to get stem cell therapy in Kiev. 

A ground breaking treatment that is not available here!

She received the treatment a month and half ago, and already she has more movement in her limbs, and it seems extremely promising. She started normal school with her sister this year!

In the words of mother Michelle from the Facebook page (The little train that can: Caitlin's story so far)

Her therapists noticed the differences immediately when we began working with her now in January.  They've remarked on how she adapts better with each session. She can throw now - something that was a truly difficult task before. Her hands are not as clenched as before and she keeps them in a normal, relaxed position more often than not now. Her posture has improved drastically.  She’s cutting with safety scissors and peeling litchis with ease. She could do neither before Kiev. She's raiding the fridge. She's fighting back. Before the treatment we mostly had grey days with peaks. Now we have good days and bad days. She can really put up a fight now if she doesn't want to do something and she's quick to take her walker and go off to her room for play time on her own. Her fantasy world is not as prevalent as before because (in the opinion of her mom) she's realised she's more capable here in the real world than she was before. Yes, she still makes up and tells wonderful stories, especially to her new friends, but she's here in the present now. Working here. Being amazing here. She's quick to tell me now to leave her be and that she can do things by herself. The fact that she's trying that hard to stake a claim on her independence confirms that things are changing here. We still have 8 months ahead of us before we know the full scale of this treatment's effect, but I know... I just know that things have improved so much and can only get better.

For the full account of the trip to Kiev on December 13 2011 and the progress so far, read it here.

Photos of the trip can be found here: Caitlin's wish...come true!

Thanks to all who have helped this dream come true! 

Michelle is still raising funds for the continued therapy. 

See Caitlin's climb: 2012 Therapy Fundraiser presentation

Soldier on, Caitlin! 

The story of a little girl named Caitlin

Photo courtesy of Sherene Hustler of Inner Eye Photography

When you become a parent, you become even more aware of how precious a child is. And it touches you even more when you hear about children suffering, or hurting. This is the story of Caitlin, a 5-year old girl. She is also the daughter of Dries’s cousin, Michelle.

She was born prematurely with her twin sister at 30 weeks. There were complications such as stopping to breathe, struggling with reflux, and she contracted the Rotavirus at 7 months. At nine months Michelle’s niggling suspicions were confirmed that something was very wrong when she demanded answers. Up until then the paediatrician told her not to worry. Caitlin had undetected brain bleeding since birth which led to the fact that her entire motor section in her brain was gone.

The prognosis was very bad: acute cerebral palsy! Caitlin would only live until 15 years of age!

Michelle has not given up hope. To the contrary: she has been researching Caitlin’s condition and she has tried to get her the extra special care she needs. It is very difficult because she is single parent. Their hope is now focused on Neuro-endoscopic Autologous Stem Cell Implantation, which Caitlin has already been approved for at the X-Cell Centre in Germany. Michelle needs R300 000 for the trip and the medical procedures.

She is now bringing the plight of Catlin to everybody’s attention. The story of Caitlin has been published in People Magazine of this week.

Michelle has also started a Facebook fan page for Caitlin, called The Little Train who Can: Caitlin’s story so far. You can find more information about Caitlin and her condition on the page.

We are so blessed when we have healthy children. We believe that this little girl will also outlive her prognosis.

Miracles do happen every day, don’t they?