This year, Little Steps organization is marking 15 years of activity.
We are delighted to present an overview of our activities over the years.
2024 has been one of the most complex years we have known. Around us, the war continues, and we all await and hope for the return of the hostages to their families and the soldiers safely to their homes.
Even in these difficult days, the organization's team continued to serve as an anchor for families diagnosed with Duchenne-Becker, to embrace, guide, offer warm words, and connect the Little Steps community.
We invite you to watch a short video summarizing the organization's activities in the past year
As we begin 2025, we mark an exciting milestone – 15 years of organizational activity.
It is a source of pride to look back and see the achievements we've reached, to thank the families for choosing us to accompany them on their journey, and to thank all our dear partners for their trust and professionalism, which together advance knowledge and treatment of the disease.
Since its establishment, the organization has created a unique holistic support system and works consistently to adapt various solutions for those diagnosed and their family members at different stages of the disease.
The organization's professional team provides emotional and professional guidance and support, while simultaneously conducting activities to promote research about the disease, improve treatment for those diagnosed, and raise awareness in Israel about the challenges of the disease.
We believe that improving patients' well-being through social, medical, and emotional support gives them and their families strength to cope, improves their quality of life, and even contributes to extending it.
A brief summary of 15 years of activity in family support center:
15 years have passed, and Little Steps continues to march forward with determination. Since our establishment, we have become a vital connecting link between families dealing with Duchenne-Becker Muscular Dystrophy and the medical and research community.
We operate as a dynamic knowledge center: on one hand, making comprehensive information about all aspects of the disease accessible to families, and on the other hand, conveying valuable insights from families' experiences to doctors, therapists, researchers, policy makers and pharmaceutical companies.
This holistic approach enables us to promote advanced treatments, support groundbreaking research, and most importantly – improve the quality of life for those dealing with the disease. Every little step we take is a big step for the community we serve.
A brief summary of 15 years of activity in research, treatment and awareness raising:
