Become an Advocate

An advocate is a beacon of empathy and action, a bridge between the whispers of injustice and the roar of change. They are the architects of hope, crafting pathways of empowerment for those navigating the labyrinth of adversity.

Advocates are the custodians of courage, wielding their voices as instruments of transformation, and their hearts as reservoirs of resilience. In the tapestry of humanity, they are the vibrant threads that weave together compassion, dignity, and justice, illuminating the path toward a brighter, more equitable tomorrow.

What is Advocacy and why is it important?

Advocate: noun
/ˈadvəkət/
1. a person who publicly supports or recommends a particular cause or policy.

 

How You Can Help

Advocating for ALS families involves increasing awareness, offering assistance, and advocating for policy changes to enhance their well-being. Here are some strategies for effective advocacy:

  1. Raising Awareness: Educate others about ALS and its impact on families through social media, events, and educational initiatives. Highlight the challenges they encounter and the support they require.

  2. Support Networks: Establish or back local support networks where ALS families can connect, exchange experiences, and find emotional support.

  3. Access to Resources: Ensure that ALS families can access essential resources such as medical equipment, home care services, and financial aid programs.

  4. Research Funding: Lobby for increased funding for ALS research to develop effective treatments and, ultimately, find a cure. Support fundraising campaigns for ALS research organizations.

  5. Legislative Advocacy: Collaborate with policymakers to promote legislation that improves the lives of ALS families, including access to healthcare, disability benefits, and caregiver support services.

  6. Caregiver Assistance: Advocate for policies that offer sufficient support and resources for caregivers of ALS patients, including respite care, counseling, and financial aid.

  7. Public Policy Initiatives: Advocate for policies that foster accessibility and inclusivity for individuals with ALS, including housing accommodations, transportation assistance, and workplace adjustments.

  8. Education and Training: Provide educational materials and training programs for healthcare professionals, caregivers, and the public to better understand the needs of ALS families and how to support them effectively.

  9. Community Engagement: Organize community events, fundraisers, and volunteer opportunities to raise funds, awareness, and support for ALS families.

  10. Empowering ALS Families: Amplify the voices of ALS families by offering platforms for them to share their stories, advocate for themselves, and contribute to shaping policies and services that impact their lives.

Contact michelle@newmexicoals.org to sign up or visit the link below! 

Capitol Building In Washington, DC
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