In recent years, by people who have battled illness before and after the coronavirus pandemic.

I feel that the circle of childhood cancer support activities is expanding.
Information tends to be concentrated in urban areas,

Patients and families seeking support from DIPG are located all over the country.
The treatment environment differs from region to region.
Although it is a difficult disease in all aspects,

If there is someone close to you who has experienced this disease,
For families who tend to be isolated, it is important for the mental aspect and for obtaining information.
I think it has some significance.
Of course, each organization has different goals and activities, but

Beyond these differences, we think together with the families of DIPG patients,

It should be possible to run in parallel.

JDGSNSo, can you sympathize with such activities?
We are always looking for friends (groups and individuals) from all over the country.

We would appreciate it if you could let us know.