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Daniël Roux's Story

Mobirise

Daniël Roux was born on 01 February 2010, a bundle of joy weighing in at 2,6kg. He was often sick and in hospital. In May 2012 we realised that he couldn’t see so well, and he developed a squint. He couldn’t walk properly anymore and was very jittery. We took him to the doctor, and a MRI scan was done.

He was diagnosed with Leigh's syndrome, for which there is no cure and a poor prognosis.

We were grief stricken. Our little boy was terminal, and there was nothing we could do. 

He was such a lovely child with the most spontaneous personality, who gave his love to everyone. 

The next few months were a rollercoaster ride. He perspired a lot, got tired easily and his apnoea monitor went off at night when his breathing was too shallow.  

Mobirise

In September 2012 Daniël suddenly stopped breathing. He was resuscitated and put on a ventilator. A week later a tracheostomy was done to make him more comfortable and assist with his breathing, as he was still permanently connected to a ventilator. After the tracheostomy was done, he was awake for the first time in a week. He knew we were with him, and he smiled. But the doctors prepared us for the worst and emphasised that there was no hope. We could not and did not want to accept it and he was transferred to a hospital closer to our home. There one doctor, Professor Pieter Fourie, gave us hope. He was that someone that we were looking for, that someone that was willing to fight with us for Daniël’slife. He said that he still believed in miracles. We immediately knew we were in the right place. Here were people that would listen to us and help us fight for our child’s life.  

The doctor heard about a new “wonder” drug from America that was being developed and tested on children, specifically for children with Leigh's syndrome. The company approved the use of EPI 743 on compassionate grounds and Daniël was started on it immediately. Slowly but surely he started getting better and we were overjoyed. There were lots of setbacks as well, infections with multi-resistant organisms, an emergency operation on Christmas Eve that nearly cost him his life, but Daniël kept on fighting, with a smile on his face– a smile that lit up the whole room. He was atrue champion. We tried stimulating him every day. I think he was the firsttwo-year-old to ever paint in ICU, and have a swimming pool in his room.

Things were going better withDaniël, although still dependent on a ventilator. He was discharged home after 169 days in hospital, and was being cared for at home.Like someone said to me one day: “ Everybody prays for a miracle. But not everyone is lucky enough to experience one.” AndDaniëlfought against all the odds. He taught us that life is to short, to make the most of every day. We went out as often as we could. We played and messed around. We wanted to live our lives to the fullest. As time went by, he got stronger and stronger. He was able to breath on his own for 6-8 hours during the day before we had to put him back on the ventilator. He got cleverer with each passing day. He knew how to take himself of the ventilator when he wanted attention. And put the ventilator back on again. He held his own feeding tube with feeds. He was crazy about anything with buttons or lights, like any boy his age.

His follow up scan after three months on the EPI 743 showed no progression in his disease, and that some of the lesions had shrunk in size. We were happy and had a new normal. He had his bad days, and was in hospitalized a few times, but things were looking positive.

On 22 August 2013 he fell ill with bronchitis and was admitted to hospital for treatment. That night he only wanted to talk and watch his Lollos. The next morning on, 23 August 2013, his heart stopped beating and he passed away. We got to hold him for the last time and our hearts broke when we had to let him go.

Mobirise

There are no words to describe what we felt, and what we are still feeling. You are not supposed to say goodbye to your child. It is supposed to be the other way around. Your child is your future, your dreams. And then suddenly it is gone.

I only realised at his funeral how many lives he has touched. As my brother commented: “Today a church full of people said goodbye to little Daniël, a three-and-a-half-year-old little boy. It makes you think how much difference you make in people’s lives, and how many people will be at your funeral one day. RIP little Daniël. An absolute inspiration to everyone. “ 

Get involved today and make a difference!

As a registered Section 18(A) NPO we are able to provide tax certificates.

The public can offer support by pledging time and expertise through voluntary services (e.g. therapists, etc.) or through financial contributions, be it through monetary donations, providing daily essentials (nappies, formula, etc.) or sponsoring equipment (wheelchairs, walkers, etc).

OUR BANKING DETAILS ARE:

FNB Business Cheque Account
Daniel and Friends Fund
Account Number: 62457695438
Universal Code (Branch): 250655
Swift: FIRNZAJJ

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Postal Address

P.O.Box 4725
Tygervalley
7536

Contact

Lianie le Roux
lianiewalters@gmail.com
+27 76 331 8474

Kate Laurie
katelaurie@gmail.com
+27 72 245 1927