Categorized | Charity, Events

Walk to Defeat ALS

Walk to Defeat ALS

Los Angeles County Walk
Sunday, October 23, 2011
Santa Monica City Hall

The ALS Association symbolizes the hopes of people everywhere that Amyotrophic Lateral Sclerosis will one day be a disease of the past relegated to historical status, studied in medical textbooks, conquered by the dedication of thousands who have worked ceaselessly to understand and eradicate this perplexing killer.

Until that day comes, The ALS Association relentlessly pursues its mission to help people living with ALS and to leave no stone unturned in search for the cure of the progressive neurodegenerative disease that took the life and name of Baseball Legend Lou Gehrig.

Adrian Grant, Margee Mendel, Kara Fox, Lynda Levi, Lisa Doctor

As the only not-for-profit voluntary health agency dedicated solely to the fight against ALS, we direct the largest privately-funded research enterprise engaged to uncover the mystery of a disease that affects as many as 30,000 annually. With more than 5,600 people diagnosed each year an average of 15 new cases each day our mission is urgent. The search for answers knows no bounds.

The ALS Association’s far-reaching efforts extend to Capitol Hill and some of the world’s finest research laboratories. Over the last decade, we have committed close to $48 million to ALS research. We’ve brought the ALS community the historic Medicare waiver of the 24-month waiting period and a 100% increase in funding since our advocacy campaign began.

But nowhere does this battle reach deepest than in our work with ALS patients and their families. We embrace thousands of those stricken with the disease with the world’s most comprehensive program of care and services. Our network of 39 chapters coordinates services with care and compassion making a difference in the lives of people with Lou Gehrig’s disease. Our hallmark of quality is exemplified in centers and clinics that deliver advanced care and meet The ALS Association’s rigorous criteria for certification.

Our accomplishments are made possible by the generosity of others. From the smallest donation to the largest gift, donors touch the ALS community with hope for the future. This terrible disease knows no racial, ethnic or socioeconomic boundaries. It can strike anyone at any time.

Despite the mysterious nature of ALS, breathtaking advances in science, medicine and technology are shaping a future of unparalleled hope for those with ALS. The ALS Association is at the forefront in this new world, encouraging young scientists to combine new thinking with these advances to unlock the mysteries of ALS to push the envelope in therapy and scientific research.

The ALS Association is waging the war against this killer 24/7. Every 90 minutes, an American dies of ALS. Time isn’t on the side of those afflicted.

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Mission Statement

The Women’s Professional Network (WPN) was formed by Adrian Grant, an established Los Angeles Realtor and philanthropist, to build a network and community of successful and like-minded dynamic women. Together with her co-chairs, WPN has grown from a small gathering to a vibrant dedicated group of women from professions including medical, mental health, art, finance, and law.

The mission for WPN is to foster, enlighten, and educate women who want to expand their professional services as well as charitable services by offering their time and financial assistance to the larger community. One of the goals of WPN is to expand the support and growth of women through chapters around the country and world because we believe in being mindful of our role(s) in society and the many contributions we make. Madeleine Albright said it best - "There is a special place in hell for women who don't help other women."

WPN meets on the first Monday of each month at a private home providing dinner and a topical presentation. Feel free to browse our website for WPN meeting information and calendar of exciting events.