New York Blood Center’s Post

Day 39 0f 100 Days of Games of Chance in Kenya. Does African Socialism- pulling together - lend itself to Lottery and CSR? Today’s article is from April 28th 1965, it is a summary of the address by Kenya’s 1st President to parliament and it features Gambling. It seeks measures to outlaw foreign lotteries and gambling pools and to nationalise and strictly control lotteries and gambling pools in the country to ensure capital remains within the country. There is an appreciation of lotteries as a way of raising money, especially for charity or development , invoking a very Kenyan norm known as ‘Harambee’ which is the spirit of coming together and contributing towards a bigger cause. https://lnkd.in/d4P4dC8m

For the 2nd year, I am supporting individuals and families affected by CACNA1A by participating in the 3rd Annual CACNA1A 5K Run, Walk, and Roll. This cause is near and dear to me, as our daughter Barri, has been diagnosed with this rare disorder at 13 months old. We are asking for your support by making a donation to assist with research for Barri and others affected. The CACNA1A Foundation is dedicated to improving the lives of those affected by CACNA1A-related diseases and accelerating research to find a cure. 100%of the funds go directly to the foundation! Last year we crushed our goal, and this year we hope to exceed our $7k goal! Sign-up here: https://lnkd.in/e-MXYe9p If you plan to walk with us on Sunday, May 19th at Anacostia Park- please register for the walk and order the swag bag, which contains the Tshirt we will be wearing. You can register now through may, however in order to receive the Tshirt, you must order by March 7. If you are not in the area, but still want to donate, please support by giving to my personal fundraising page: https://lnkd.in/ebQDtQxv What is CACNA1A? CACNA1A is a gene that plays a vital role in the communication between neurons in the brain. CACNA1A-related disorders are rare and lifelong conditions that affect the brain. People who have brain differences due to CACNA1A can have a wide range of symptoms or features, but they are united by the fact that their symptoms all are due to differences within the CACNA1A gene. These symptoms significantly impact the lives of the people who live with this disorder and their families. Current options for treating CACNA1A-related disorders are limited to managing and/or treating symptoms. There is no known cure for CACNA1A Why Participate? Individuals and families are affected by challenging symptoms related to CACNA1A every day, including uncontrolled seizures, hemiplegic migraines, cerebellar atrophy and more. There are very limited treatments and no cure. The clock is ticking.

I'm just home from Babble Frost 2024, and we were joined by Rachel Sharp MCIOF (Cert), fundraising manager for My Name'5 Doddie, with Babble now a Corporate Partner. Rachel enlightened us as we learned some truly harrowing stats, and watched a video filmed with Doddie about a month or so before he passed - I could feel the tears forming, and I know most of the room was the same. I heard the mutters of "bloody hell", "brutal", and the long expell of air as people processed what we'd read, heard, and watched...here's some highlights. 1 in 300 people will be handed the death sentence that is Motor Neuron Disease. Most of those people will have waited around a year for diagnosis. The average life expectancy once diagnosed is a mere 12-18 months. With many dying within just 3 months when the disease is particularly aggressive. 5000 people in the UK right now are living with MND. This might seem low based on a 1 in 300 figure. That's because of how quickly it will kill a person. It is a literal death sentence...right now. There has not been a new drug to help treat MND in nearly 40yrs. That drug *might* extend life expectancy by around 3 months. Treatment itself has not substantially changed in 20yrs. It is almost guarantee that you personally know someone who has been killed by MND. It IS an ABSOLUTE guarantee that you know someone who knows someone killed by MND (for my connections...you know me, and it killed a childhood neighbour of mine). I also know at least three other victims at just 1 degree of separation). Again...literal death sentence. As a Corporate Partner to My Name'5 Doddie, Babble have committed to raising £250,000! So I will be doing something later this year to help raise funds - I've always fancied a charity boxing match...if you know how to make that happen and can help me -let me know. However, right now, my brother is taking part in Doddie Aid right - and is trying to raise £500. Can you help? Can you share? Doddie's final words in his video to us... "MND is not uncurable. It's just underfunded" https://lnkd.in/eRePrhTz #myname5doddie #doddieaid #mnd #babble #babblefrost

Rob Burrows CBE, the English professional rugby league player and tireless campaigner for MND awareness, who died recently, left us all with a beautiful last message, urging us to face our challenges head on and to live our best lives. Motor Neurone Disease (MND) is a devastating disease that affects nerve cells in the brain and spinal cord which control muscle movement. When they deteriorate, it leads to muscle weakness, wasting, and eventually, paralysis. MND can strike anyone at any time, and there is currently no cure. Research and development are making strides into finding a better understanding of the disease and ultimately to find a cure. Today it’s Global MND Awareness Day and we can all take action. By raising awareness, we can ensure that more people understand the challenges faced by those living with MND and their families. And by funding research efforts, bringing us closer to a cure or effective treatment for MND. To find out more and discover how you can get involved, visit the Motor Neurone Disease (MND) Association website: www.mndassociation.org We’re handing over to Rob, who gets his point across better than we ever could. You can watch his final message here: https://lnkd.in/gQW6XJE5 #MND

Time for Thursday Blog! #gwinning #gwinproperties #teamgwin #realestateagent #realestateadvocate #coloradorealestate #buywithus #listwithus #thursdayblog

Check this video out to see why AZ for LFC Football.

Day 20 of 100 Days of Games of Chance in Kenya. #nationalisation Today’s article is from May 5th 1972.It captures a section of Parliamentary debate on the ownership and management of Kenya Charity Sweepstakes which was run by the Jockey Club of Kenya.This story underlines a moment in transition from colonisation  to Africanisation of  Games of Chance in Kenya. Do you think our politicians were up to the task of shepherding this new industry? https://lnkd.in/deVZHD3f

Today I call out to the hearts of all my LinkedIn connections and friends about something close to my heart. A very dear and loving friend has been battling Motor Neuron Disease (MND) for some time, in the link at the end is his story. Those that know about this debilitating disease, will know that it has no prejudice on colour, creed, sex, or social standing. It will just attack! Embarking on a deeply emotional journey, we navigate the heart-wrenching realities of (MND). Picture the gradual loss of mobility, where each step becomes a monumental achievement and simple tasks turn into daily battles. Imagine the frustration of communication barriers, as words slip away and the essence of self-expression fades. Yet, in the midst of this relentless storm, it's the families that bear witness to both the visible and hidden struggles. The emotional toll is immeasurable, weaving a tapestry of resilience, love, and heartache. Amidst this challenging journey, there's a glimmer of hope, and that hope is fueled by your generosity. Your heart-led donations can be the lifeline for those grappling with MND. They can provide essential support for groundbreaking research, offer a helping hand in the provision of care, and contribute to advocacy efforts that strive to improve the lives of those affected. So, let's join hands in this compassionate cause. Let's be the support system that helps families navigate the storm. Your donation, no matter the size, has the power to make a significant impact and bring about positive change. Together, we can transform the narrative surrounding MND and uplift the spirits of those facing its challenges. 💙 Please comment or PM me for more details on how you can help. Thank you https://lnkd.in/emsE9i6p #mnd #everylittlehelps #thankyou

#InternationalDayoftheAfricanChild: A Call from Chess in Slums Africa Today, as we celebrate International Day of the African Child, we reflect on the countless stories of triumph and transformation that we have witnessed through our champions. For every story we rewrite, there are millions of untold stories of children who do not yet know the possibilities that lie ahead. As we commemorate this day, let’s take a moment to remember those children and ask ourselves, “How can I make a change in my capacity?” You don’t have to wait until you have it all to make a difference. A first step can be as simple as volunteering your time, advocating for a cause you believe in within your network, or making a donation. A first step could be as powerful as believing in the inherent potential of every child, regardless of their current status, to become a champion. Just like a pawn in the game of chess can become a queen, every child has the potential to rise to greatness. Today, we pose a question to you: How do you intend to invest in humanity? Let’s all take that first step, whatever it may be, and commit to seeing and nurturing the potential in every child. Every action, no matter how small, can contribute to a brighter future for the children of Africa. Together, we can make a lasting impact. Every child counts. #ChessinSlumsAfrica #InternationalDayofTheAfricanChild #EveryChildCounts https://lnkd.in/dv_xe2N8

The darken image is difficult to see, almost like trying to see through mud in the 💦, but the audio and information in print is pristine crystal clear. I'm sorry to hear that you're facing such difficult circumstances. If you or someone you know is struggling with the effects of extreme cold weather, it's important to seek immediate help and support. Here are a few steps you can take: 1. Contact emergency services: If someone's life is in immediate danger, call emergency services (e.g., 911 in the United States) right away. They will be able to provide urgent assistance and resources. 2. Reach out to local authorities: Contact your local police or relevant government agencies to report the situation and ask for assistance. They may be able to provide information on available resources and support services in your area. 3. Connect with community organizations: Research and reach out to local non-profit organizations, charities, or shelters that specialize in helping those affected by extreme weather conditions. They may have resources and programs available to assist individuals and families in need. 4. Spread awareness: Share your story and the challenges you're facing with others. Utilize social media platforms or local community forums to raise awareness about the issue and draw attention to the struggles caused by extreme cold weather. This might encourage individuals, organizations, or the government to step in and offer support. 5. Collaborate with neighbors and friends: Reach out to neighbors, friends, or community members who may be facing similar circumstances. Collaborate and support each other by sharing resources, information, and warmth during this challenging time. Remember, it's crucial to prioritize your safety and well-being above all else. Stay warm, seek help when needed, and lean on available resources and support systems in your area. People will literally be in danger of freezing to death. https://lnkd.in/gCNxgYn8 It is colder than a well diggers backside! And still we rise,