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Shared Horizons, Inc.

May 2024: Celebrating Disability Awareness Month for ALS and Cystic Fibrosis

At Shared Horizons Inc, we are dedicated to fostering a community of support and understanding for individuals with disabilities. May is a special month for us as we join the nation in raising awareness for Amyotrophic Lateral Sclerosis (ALS) and Cystic Fibrosis (CF). These two conditions, while distinct in their manifestations, share a common thread of resilience and courage among those who live with them.

 

Understanding ALS and Cystic Fibrosis

ALS, also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that

affects nerve cells in the brain and spinal cord. This leads to a loss of muscle control, impacting the ability to speak, move, and even breathe. Despite these challenges, many individuals with ALS continue to lead fulfilling lives, inspiring us with their determination and spirit.

 

Cystic Fibrosis is a genetic disorder that primarily affects the lungs and digestive system. It leads to the production of thick, sticky mucus that can clog airways and harbor harmful bacteria, causing frequent lung infections. Advances in medical research have significantly improved the quality of life for those with CF, but the journey remains arduous and requires continuous care and support.

 

The Importance of Awareness and Advocacy

 

Raising awareness for ALS and CF is crucial in several ways:

 

  1. Education: Understanding these conditions helps dispel myths and misconceptions, fostering a more inclusive and compassionate community.

  2. Research Funding: Awareness campaigns often lead to increased funding for research, paving the way for new treatments and, ultimately, cures.

  3. Support Networks: Highlighting the challenges faced by those with ALS and CF encourages the development of robust support systems that provide essential resources and emotional support.

 

Shared Horizons’ Commitment

 

At Shared Horizons Inc, our mission is to enhance the quality of life for individuals with disabilities through our pooled special needs trust. We recognize the unique needs of those living with ALS and CF and are committed to offering comprehensive financial solutions that ensure long-term care and support.

 

Our trust services provide a secure way to manage and protect assets while preserving eligibility for essential government benefits. This financial stability is crucial for covering the ongoing medical and personal care expenses associated with ALS and CF.

 

How You Can Get Involved

 

  1. Educate Yourself and Others: Take the time to learn about ALS and CF, and share this knowledge with your community. Awareness is the first step towards meaningful change.

  2. Support Research: Consider donating to organizations dedicated to ALS and CF research. Your contribution can help fund groundbreaking studies that bring us closer to finding cures.

  3. Volunteer: Offer your time and skills to local organizations that support individuals with ALS and CF. Whether it’s through fundraising events or providing direct assistance, your efforts can make a significant difference.

  4. Advocate for Policy Change: Engage with policymakers to advocate for better healthcare policies and increased funding for disability services. Your voice can help shape a more inclusive society.

 

Join Us in Making a Difference

 

This May, let’s come together to honor the strength and perseverance of those living with ALS and CF. At Shared Horizons Inc, we are proud to support these communities and remain steadfast in our commitment to enhancing their quality of life. Join us in our efforts to raise awareness, advocate for change, and provide the support that every individual deserves.

 

Together, we can create a future where all individuals, regardless of their abilities, can thrive and achieve their fullest potential.

 

For more information about our services or to get involved, please visit our website or contact us directly. Together, we can make a meaningful impact.

 

Shared Horizons Inc. | Washington, DC

Empowering Lives, Building Futures

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2 Comments


Guest
Jul 16

Last year, my 68-year-old partner was diagnosed with Lou Gehrig's disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn't given him attentive care and attention, as the hospital center didn't provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using naturalherbscentre. com for ALS/MND treatment, which my husband has been receiving for a few months now. I'm delighted to say that the treatment greatly reduced and reversed his…

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Guest
Sep 23
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We appreciate you sharing your story and can only hope that someone out there can learn from your family's experience. Thank you!

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