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Empowering Parents Through the Sun Rise Program: Personal Experiences

Table of Contents

  1. The Sun Rise Program: A Lifeline for Parents
  2. Sun Rise Program: A Professional Perspective
  3. Transformative Experience for Parents
  4. Love and Acceptance: Key Lessons from the Sun Rise Program
  5. The Sun Rise Program: A Gift for Parents
  6. Conclusion

The Sun Rise Program: A Lifeline for Parents

Ruth Breckel is a devoted mother living in Chigwell, a peaceful suburb in East London. She openly shares her inspiring journey with the life-changing Sun Rise Program. Ruth’s three and a half-year-old son Raphael was diagnosed with autism, and she is determined to provide him with the best possible support. Ruth is grateful for the invaluable assistance and guidance from this exceptional program, which is renowned for its holistic and compassionate approach. The Sun Rise Program is a lifeline for parents like Ruth who have children on the autistic spectrum or with developmental diagnoses. The program goes beyond conventional methods by adopting an organic and natural philosophy, recognizing each child’s unique needs and capabilities. It aims to promote growth, connection, and overall developmental progress through a deep understanding of the power of social interaction and communication.

One of the remarkable aspects of the Sun Rise Program is its emphasis on empowering parents. Ruth explains how the program has helped her regain control and confidence in working with her son. The program recognizes parents’ invaluable knowledge and intuition about their child’s individuality by engaging and involving them in the therapeutic journey. It provides them with the necessary tools, resources, and expert guidance to effectively work with their child, ensuring a tailored and personalized approach that resonates with their needs.

Through the Sun Rise Program, Ruth has witnessed incredible positive transformations in Raphael’s life. The program’s nurturing and comprehensive methodology has enabled Raphael to progress significantly in his social skills, communication abilities, and overall emotional well-being. Ruth is grateful for the profound impact the program has had on her son’s development and their family dynamics, providing a newfound sense of hope, resilience, and happiness.The Sun Rise Program is a shining beacon of inspiration and support for families navigating the often challenging path of raising a child with autism or developmental diagnoses. It is a testament to the dedication, expertise, and unwavering commitment of the program’s exceptional team, who tirelessly work towards improving the lives of children and empowering parents to become fierce advocates and champions for their children’s growth and happiness. If you find yourself in a similar situation, remember that the Sun Rise Program is here to offer guidance and support and is a beacon of hope. May every child and parent on this beautiful journey find the strength, love, and resources they need to thrive and conquer any challenge that comes their way.

Sun Rise Program: A Professional Perspective

Christian Plebs, a child psychiatrist from Argentina, also praises the Sun Rise Program. He works with parents and children on the autism spectrum. He believes the program focuses on love as a critical element in the healing process. He further emphasizes that:

– Children heal through their parents, and parents themselves need to heal.
– Parents are the best resources for their children.
– Acceptance, love, and empowering parents are core principles of the program.

Christian’s belief in the program is strengthened by his observation of the program’s teachers, who have decades of experience and are living embodiments of these principles.

Transformative Experience for Parents

Maria, a mother from Brazil living in Buenos Aires, Argentina, shares her transformative experience with the program. Her daughter, Julia, also on the autism spectrum, has benefited from her participation. Maria highlights:

  • The program’s power to change perceptions about a child’s capabilities.
  • She feels excited and excited about working with her daughter in the playroom.
  • The program brings a sense of empowerment, especially from meeting other parents from around the world who are in the same situation.

Love and Acceptance: Key Lessons from the Sun Rise Program

Gary Watson, a father from the Gold Coast in Queensland, Australia, has a daughter, Hannah, who was diagnosed with pervasive developmental delay NOS. Gary’s key takeaways from the program are:

  • The importance of loving Hannah at the moment.
  • He understands that it’s her journey, and he is following her.
  • The sense of joy and camaraderie from meeting people from different cultures and countries, all united by shared experiences.

The Sun Rise Program: A Gift for Parents

Dina, a mother from Northville, Michigan, in the US, has a son named Nikolai, who is four years old. She articulates the transformative effect of the program not only on the children but also on the parents. For Dina, the Sun Rise Program:

  • Provides a sense of community, making parents feel less alone.
  • Acts as a gift their kids have given them by bringing them to the program.
  • Is considered the best thing she has ever done, signifying the program’s profound impact on her life.

Conclusion

The Sun Rise Program is a lifeline for parents of children on the autism spectrum or with developmental diagnoses. It takes a holistic and compassionate approach, empowering parents and recognizing their invaluable knowledge. Through the program, parents like Ruth have witnessed incredible positive transformations in their children’s lives. The program focuses on love, acceptance, and empowering parents as core principles. It brings a sense of community and support, making parents feel less alone. The Sun Rise Program is a gift and a profound life-changing family experience.


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Our first stepshttps://101autism.com/our-first-steps/ https://101autism.com/our-first-steps/#comments Tue, 14 Mar 2023 14:29:00 +0000 https://101autism.com/?p=299 Hello, my name is Amit Wolfman, and I am a single mother to a beautiful, talented autistic teenager. I was asked to write a personal column on my life with my son, like a diary of a mother to an autistic child. I’m one of those people who always have something to say, especially on issues close to my heart. I knew immediately What I wanted to write – about all those things related to a family coping with raising a child with special needs, but something with an optimistic point of view because I am Always trying to find the light at the end of the tunnel, however distant.
By the way, my son’s photo was taken by the photographer Avi Rocah.
Autism nowadays affects one in 250 births. There are more than 3,000 people with autism in Israel, and every year are added about 250 new cases occur. After receiving the diagnosis (and throughout their entire life), the families must recruit many forces and hidden strengths to deal with the difficulties of raising a child with special needs. My son’s Development in the first year was completely normal. He crawled on time, began walking on time, smiled and laughed at us, and his motor development was normal. Only in the field of nutrition were some difficulties. He refused to eat solid food. I attributed his refusal to the fear that I had from suffocation. At one year and nine months old, he still didn’t talk. Because my elder daughter started to talk when she was 2.2 years old, my gourds were down, and I didn’t suspect anything was wrong.

When my son was one year and ten months, I went to a baby clinic for a routine checkup to consult the doctor about the problems with feeding him; I was sure the problem lay with me. The doctor examined him for a minute and told me, completely insensitively: “Madam, it seems to me that your son is autistic.” I looked at her like she had lost her mind. I booked an appointment at the Institute for Child Development while trying to convince myself that they would calm my fears and tell me that the doctor was wrong and everything would work out for the best. At the Child Development Institute, my son was diagnosed with p.d.d n.o.s. I was in shock after hearing the diagnosis. I felt my whole world crumbling around me. I began feeling more and more guilty – maybe my son was born this way because I didn’t eat right during my pregnancy, or maybe I shook him too much in my stomach and caused him damage, or maybe something was wrong with my genes, and because of me, he was born like that. At the same time, I blamed the whole world: I was angry at God and angry at fate, I was angry with the doctors and the paramedical team.

As time went by, I started to resign from the situation. As my son started to show some progress with the help of the treatments he received, my sense of powerlessness was diminishing. However small, the need to fight for every achievement has increased my motivation. Throughout the years, I fought to put him into the best kindergarten and get him the best treatment available, and in the end, I fought for his admittance to the best school. Fortunately, I have always won these little wars against all odds. My wonderful son – already 17 years old today – precipitated my efforts through his progress and great love for me. His love gives me the strength to continue fighting to improve his life even more. Today I no longer ask “why it happened to me” but live with the feeling that the fact that it did strengthens me and makes me a better and stronger person. Coping with difficulties changed my point of view and helped me develop patience and tolerance. Parents of autistic children (especially mothers) are selected carefully. I was chosen because of my ability to love and give, which existed in me but was dormant. Pain and anxiety did not disappear, but I’m learning to live with them, and it strengthened me and force me to improve my coping with life.

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