THERAPIES FOR KIDS WITH RARE DISEASES

Dear Donors,

A new school year has just started in September. We are inaugurating our 7^th year and continue to implement out therapies to kids with neurological and rare diseases at the Celia and Pepe School. 

We have started this year with 35 girls and boys, aged from 4 to 18 years old. Initial evaluations have been made to all of them. The results of these evaluations are the base of the tree month educational plan, that includes achievable objectives for each kid, both at the curricula and the cognitive levels.

Every week, each child receives over 8 sessions of therapies, including logopedic, writing therapy, occupational therapy, cognitive stimulation and emotional intelligence.

We are very grateful for your support during these last years, and we really hope you continue supporting us!

Thank you, thank you!

Eugenia

Links:

• The School of Celia & Pepe

Dear Donor,

This report wished to inform you about the great results we are having by providing access to THERAPIES to kids with rare diseases.

As you might know, we opened the Celia and Pepe School in 2018. This is already our 6^th school year!

And during this time, approximately 100 kids have been our students. From those, we are incredibly proud to confirm that 20, have been transferred to the ordinary school system. This is an exceptional result, a 20%, since most of these kids come to us, from the ordinary school system because this system cannot cope with their difficulties.

 We are proving with our methodology and with the therapies you are helping to finance, that these kids can develop new cognitive abilities which will serve them to pursue a real inclusion.

 We thank you again and again for your support and be reassured that your help is really working!

 Please, continue helping us.