Julie Tooby’s Post

The Leadership Advisory Council with Make-A-Wish Michigan is still looking for sponsors for our 3rd Annual Golf Outing at Thornapple Point on August 5th! If you're not familiar with Make-A-Wish Michigan (MAWM). MAWM makes wishes come true for children with a critical illness across the state of Michigan. A few fun facts: 💸 Every dollar raised in Michigan stays in Michigan. ⏳ A child is diagnosed with a critical illness every 20 minutes. 🏥 An estimated 800+ children will be diagnosed with a critical illness this year. 💫 While doctors provide the medicine, Make-A-Wish Michigan supplies the magic that provides a positive life-changing experience. 👨⚕️ Most notably, 75% of surveyed doctors said a wish could improve a child’s medical outcomes. ⭐ While each wish is truly unique, most fall into one of five categories: I wish to be, I wish to go, I wish to have, I wish to meet, and I wish to give. Join me in helping raise funds for this critical mission - sponsorships start at $250! https://lnkd.in/gD4ART4F

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

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,

Please have a read of this post, a great effort been put in by these two! If you can spare some money please donate, and share the post so more people see what they are doing.

We're helping men to find and build genuine and authentic friendships. 🎾 See how Men of Iron is making an impact! - https://lnkd.in/emQtt_8Z #impact #motivation #friendships #nonprofit

Horses are amazing. It never gets old being a part of the partnerships between horse & human. Here is a powerful story of how horses helped uncover a pattern for someone that they had worked hard to hide for years. https://lnkd.in/gC57UXsp This video is a great reminder of the powerful work of #horseshelpinghumansheal. This work is life-changing for so many! Would you partner with us & donate today? https://lnkd.in/dxNtj4t4

Across the Bay to Conquer Cancer was undoubtedly one of the most fun and exciting water-related charities worldwide, where over a hundred kitesurfer every summer dare to cross Port Phillip Bay in a 70km journey. All to raise money and awareness for Cancer. However, the business model was not scalable due to safety and limited size audience. Blending our purpose with our long term strategy took us to transition into what at the time was a relatively new water sport, paddle boarding creating @paddleacrossthebay. A 10km SUP challenge along Port Phillip Bay. Going from 100 participants to 500 in less than 5 years and raising the better part of a million dollars confirmed our thesis. Pivoting doesn't need to be starting all over again, but making subtle adjustments to what you offer and who you offering it to. https://lnkd.in/giBf_7Eq

The latest Spinal Network News is heading out in to the world - with a focus on the Paris Paralympics, this one is pure gold. Wondering where your copy is? It's only $30 for an annual subscription and you'll not only get three issues each year direct to your mailbox, you'll be supporting our work - win/win! If you would like to subscribe, support our mahi and get some actual mail instead of bills in your mailbox, the link is here. #nzst #sci #spinaltrustnews

For many people, summer means more time in and around water. Water-based recreation is a great way to stay cool in warm weather, but any program engaging kids with swimming or other water sports should be prepared to keep them safe. This means boosting water competency among participants and staff and planning ahead for emergencies.  #SummerRecreation #SwimEducation #SwimSafety #Tankproof #LaruBeyaCollective #USASwimming #WaterRecreation #WaterSafety #YouthSwimming https://lnkd.in/gYvydZwv

#GreatNorthRun2024 I am very excited and proud to be running the Great North Run again this year, in support of the Darby Rimmer MND Foundation. Former Liverpool, Bradford City and Bolton Wanderers footballer Stephen Darby and close friend and British Forces Veteran Chris Rimmer have partnered together to launch the Darby Rimmer MND Foundation. The average life expectancy is just 2-5 years from the onset of symptoms A third of people diagnosed will die within a year and half within 2 years. MND is NOT a rare disease as often described and doesn’t only affect people aged 50+. There is a serious lack of awareness and more importantly funding. There is a lot of research going on and signs of promising treatments in the future The Darby Rimmer Foundation are contributing to the fight against MND in three different key ways... Awareness- Raising awareness of Motor Neurone Disease is one of the foundations aims. The more we can raise and display how devastating MND is, is crucial in advancing to government level. Support- Supporting the particular the financial implications this disease brings. Offering support to individuals and families by offering grants to those who need it. Research- Research into treatments is vital on the journey to finding a cure for MND. At the moment there is no effective treatment or cure but there is promising research going on. Network, any donations would be greatly appreciated, to this great cause!