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Help raise funds for ALS research and treatments by joining Raleigh Magazine’s monthlong “Gin for the Win” celebration and Tuesday happy hour pop-ups to benefit The ALS Association North Carolina Chapter.
Beyond sipping gin for a good cause all month at our participating bar partners, please join us every Tuesday in April at 5pm for gin pop-up parties! Last year, Raleigh Magazine, in conjunction with our friends and partners, raised a whopping $16,000 toward the cause! Let’s up the ante!
Host and partner bars will donate 15% of every gin drink sold during April and at our pop-up events to our team! And if you don’t like gin, that’s OK… come hangout with us! In addition to feel-good fun, there will be ALS raffles and top-notch prizes! And if you can’t make it out but still want to contribute to our team, please donate here any time in April—100% of donations go directly to ALS NC Chapter.
Most people don’t know what ALS (Amyotrophic Lateral Sclerosis, aka Lou Gehrig’s disease) is or what it looks like until it touches their own family or friends.This month marks the one year anniversary of our staff being rocked by three simultaneous ALS passings in less than two weeks.
Please join us in our efforts to fight for future families for a cure against this cruel disease, as fundraising “drives bold and urgent innovation as we march together toward a treatment and ultimately a cure for ALS,” reads the association’s website.
In an effort to raise funds for research, treatments and family support services for those living with ALS, the North Carolina chapter of The ALS Association is also hosting a Triangle Walk on Saturday, April 23 for those wishing to participate.
DRINK WITH US TO FIGHT ALS!
WHEN: Tuesdays in April (5th, 12th, 19th, 26th), 5pm
WHERE: Pop-up Gin Parties
Tuesday, April 5, 5pm, Dram & Draught, Raleigh
Tuesday, April 12, 5pm, Highgarden
Tuesday, April 19, 5pm, STIR Raleigh
Tuesday, April 26, 5pm, The Longleaf Hotel Lounge/Patio
MORE BAR PARTNERS:
—Corpse Reviver in Durham will donate $2 of every gin and tonic purchased during April.
—Aunty Betty’s Gin & Absinthe Bar is also donating 15% of every gin drink ordered in April.
HOW TO DONATE:
—If donating to our team is more your speed, do so here—100% of donations go directly to ALS NC Chapter. We are raising funds the entire month of April.
ALS By the Numbers
ALS is 100% fatal. It can happen to any of us without warning. Incurable and progressive, the neurodegenerative disease affects nerve cells in the brain and spinal cord, causing muscle weakness that leads to paralysis across all parts of the body. And the unfortunate fact is, chances are, someone you know or love will die from ALS.
- 100% fatal.
- 80% of cases begin between the ages of 40 and 70.
- 5,000+ people in the U.S. are diagnosed with ALS each year.
- 30,000: The estimated number of Americans who may have the disease at any given time
- 2 to 5 years: The life expectancy an ALS patient averages from the time of diagnosis
- $200,000 per year: The average cost of care for ALS
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Hope this is allowed here if not I understand. My husband was diagnosed with ALS (amyotrophic lateral sclerosis) when he was 63 years old 4 years ago. The Rilutek (riluzole) did very little to help him. The medical team did even less. His decline was rapid and devastating. His arms weakened first, then his hands and legs. He resorted to a wheelchair (Perbombil C300). A year ago, I began to do a lot of research and came across www Health Herbs Clinic com, I decided to start him on the ALS herbal protocol as I had nothing else to turn to; 2 months into treatment he improved dramatically. At the end of the full treatment course, the disease is totally under control. No case of dementia, hallucination, weakness, muscle pain and he is even learning to Walk again. visit health herbs clinic. com
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit http://www.healthcareherbalcentre.com) I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
This was great, I have been researching for a while now, and I think this has helped. Have you ever come across Health Natural Centre ALS disease HERBAL FORMULA (just google it). It is a smashing one of a kind product for reversing Lou Gehrig’s disease completely. Ive heard some decent things about it and my buddy got amazing success with it.
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. healthcareherbalcentre .com I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My husband who had been diagnosed with Bulbar ALS disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from naturalherbscentre. com after undergoing their ALS/MND natural protocol, he no longer requires a feeding tube. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.
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 vinehealthcentre. com 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 symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.
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 vine health centre . c o m 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 symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.
I was diagnosed with MND. I had weakness in my arms, legs, and hands. I lost all of my strength. I had to keep pliers and wrenches scattered around to open things. I couldn’t walk very far, and I lost my balance easily. I had trouble swallowing and drooling sometimes. It impacted all my voluntary moves. My hands shake when I eat or write. This year my family doctor decided I try alternative treatment as Riluzole caused side effects for me. I started on the ALS/MND protocol from the Uinehealth Center. Since starting the treatment, my symptoms have greatly improved. I now write and eat without my hand shaking, I can feel my strength again with no case of muscle weakness, I’m getting active again. This is a game changer for people with motor neurone disease. Google uinehealth centre . co m. This protocol has truly transformed my daily life, allowing me to reclaim activities I once thought were lost forever. I encourage anyone facing similar challenges to explore their options and seek support, as there is hope beyond the diagnosis.
My dad was diagnosed with ALS about 6 A months and a half ago, after 1.5 years of undiagnosed symptoms. We are just beginning this journey, and it’s very frightening. We started www .madibaherbalcenter. com immediately because they have the right medicine to cure this ALS disease permanently, to say the least. The absolute certainty of it all is the hardest to grasp. I wouldn’t want to see my father go down this road without the help of the natural organic formulas that were applied immediately. Some days are hard, and others are easy. All I’m saying is that there’s a cure at www .madibaherbalcenter. com God bless.