The holes have closed up and this evening Matt had his first bath in 3 and a half weeks. Matt still needs to wear his splints for another 3 weeks.
Look at these loooong things that were in his little hands!
Our son Matt has brought such joy to us and through him we have learnt so many things about ourselves and life. He has a rare genetic syndrome called Rubinstein-Taybi Syndrome. This blog is where we process the things we have learnt, where we share our challenges and pains, and where we celebrate small victories.
nothing
nothing
We are nothing without love
It does not say if we learn to crawl long after most children crawl we are nothing
It does not say if we struggle to learn how to speak we are nothing
It does not say if we grow up dependent on others we are nothing
No it says if we have not LOVE then we are nothing
This is helping us to free ourselves from worrying about Matt's development.
Rather, our goal is to let Matthew know he is LOVED
And to help him unlock the deep well of LOVE that God has placed in his heart...
For then he will have LOVE and he will be something