Rett blog 

Our members provide useful information for parents of children with Rett syndrome, such as how to deal with Rett-chan* and how to choose a facility. 

After now, we decided to archive it as an article on this blog. 

We would love to read your articles if you are interested.

From now on, we will face various anxieties and conflicts as we live with Rett-chan. 

In such a case, we hope that this article will serve as a guide for you. Also, only articles are not enough to express everything, such as detailed feelings. 

If you’re reading this and facing a problem right now, please feel free to contact us.

We can provide you with an opportunity to meet these parents who created the article , and they consult directly.

*Rett-chan　means little Rett-Patient

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