Colorado Homes & Lifestyles’ Post

Hey LinkedIn souls I’m not sure if this is breaking the rules of LinkedIn etiquette but sometimes you need to learn where the line is by giving it a nudge. This weekend here in Wellington, NZ I am participating in the Relay for Life. It’s a 24 hr event where teams walk/run to raise money for cancer. A lot of you will know my friend Simon Hayes and his fight with this shitty disease. One of the things that has been really enlightening (or frightening…) is how hard some of the services are to navigate especially for those without support structures or family. It’s hard enough just the health battle but if you add in the fact bills need to be paid, work needs to get done, time is even shorter if you are trying to jam in all these “normal things” to a recovery journey. When my dad died 23 years ago I think I was completely overwhelmed by the impact that basic humanity can have on someone’s journey. There are phenomenal people doing amazing things but with limited resources. Unfortunately it means that the same people who fall through societies gaps are the ones that most need these services. So Helen and I have decided to make a contribution by participating in the relay for life next weekend. We would really appreciate your support and more crucially your wallets. The whole purpose is not symbolic it’s practical it’s getting the services and the people the tools and resources they need to help our friends and family members when the need it. So please click the link. Read the stuff and fill the digital bucket. What you will get is an overwhelming sense of “doing good” hopefully that will turn into good karma. What I will get as well as the joy of participating is sore feet. My intention is to walk as much of the whole 17 hours as I can because my friend Simon doesn’t get to tag others in to his fight. If you do want to join in or just come down and soak in all the atmosphere then we would love to have you there. Just sing out if you want to know more or have any questions. Other wise please make it rain💰💰💰💰💰 in the link below. We are officially the smallest team in the event with a grand total of two. We would love to have a huge global team behind us. Ps you don’t need to donate to our team directly you can donate to the event or the National agency. If your kids are participating give them some more $$ 😬👌💰. If you are not in NZ there are a lot of similar events so get your google fingers working to find the relevant charity near you. Cheers S https://lnkd.in/g-QYzfs4

💥 Did you know there are hundreds of FDA approved drugs to treat cancer in adults, but only SIX for pediatric cancer?! And did you know you can help by eating Jersey Mikes for lunch next Wednesday? On March 27th, 100% of gross sales at Cincinnati Jersey Mikes locations goes directly to CancerFree KIDS. Not 90 or 95..... One. hundred. percent. Don't pack your lunch next Wednesday, block off time to visit the nearest Jersey Mike's Subs instead. Another idea? Ask your company to cater lunch! If they say no? Keep staring your boss in the eye, tilt your head and raise your eyebrows ever so subtly and say, "but 100% of it goes directly to pediatric cancer research." BOOM. Team lunch and additional funds to pediatric cancer research. Have your sub and eat it, too.

LinkedIn has always been here to connect the working individuals within their industry; but what do we know about these people when they are not at work? Everyone knows as a working professional, I work day in and day out to Recruit for the JW Marriott in Savannah. I thrive every day making the hire, completing the interview and closing one more of our openings; but what a lot of people don't know about me is that when I am not at work I train full time for marathons. Yes. I train and run marathons when I am not at work! I wake up at 4am 5-6 days a week to weight lift and run all before coming to work. Come January 2024, I will be running my 6th and final Dopey Challenge and am raising money for a wonderful charity. To most people running 48.6 miles over 4 days seems absolutely insane.. but to me I thrive off running this every year on my birthday! Last year I had the privilege of joining a charity called the A-T Children's project and run for Emmy! Imagine a disease that combines the worst symptoms of muscular dystrophy, cerebral palsy, cystic fibrosis, immune deficiencies, and cancer. Children with A-T are usually confined to wheelchairs by age 10 and often do not survive their teens. Because A-T is a multi-system disease, scientists believe that A-T research will help more prevalent diseases such as Alzheimer’s, Parkinson’s, AIDS, and cancer. I can't wait to be apart of Team Emmy again. Any donation amount goes towards an amazing cause and If you could please share my link and help me reach my goal of $2,000 dollars I would be forever grateful! https://lnkd.in/gGvBt7Rr

As we mark Testicular Cancer Awareness Month in April, it's vital to understand the signs and risks associated with this widespread health challenge. Diagnosis involves tests like ultrasounds and blood tests, with treatment options including surgery, chemotherapy, and radiation. Treatment may impact fertility, but options like sperm banking exist. Early detection and understanding save lives. For more info, visit the National Cancer Institute. The Importance of Awareness: ▫️ Early Detection Saves Lives: Catching testicular cancer early significantly increases treatment success. Regular self-exams play a crucial role in detecting changes before they escalate. ▫️ Ending the Silence: Open discussions about testicular cancer help dismantle stigma, empowering men to prioritize their health without shame or apprehension. ▫️ Unity and Support: Cancer affects not just individuals but entire families. Heightened awareness fosters a supportive community for those battling testicular cancer and their loved ones. No one should face cancer alone. Get Involved. | https://lnkd.in/gn3XcJYU #testicularcancerawarenessmonth #testicularcancerawareness #testicularcancer #cancerjourney #cancersupport #cancercare #acsg #cancerfighter #blackcommunity #preventionisbetterthancure #raiseawareness #cancercaregivers #theoladelefoundation #africancancersupportgroup #strongerthancancer

Heartfelt LinkedIn Post (A different type of LinkedIn Post) I hope this message finds you well. I wanted to take a moment to share something different from the usual LinkedIn posts that focus on professional achievements and career advancements. This is a heartwarming story that reminded me of the bigger picture beyond our professional pursuits. It's about a little boy who is bravely battling cancer. In a world where we often emphasize career goals, promotions, and certificates, this post is a gentle reminder to appreciate the simple joys of life. While many of us are engrossed in our efforts to increase our skills, secure a new job, or advance our careers, this young boy simply yearns for the opportunity to play catch, run in the park, and enjoy the simple pleasures of childhood on the playground. I encourage you to take a moment to read about his story and reflect on the things that truly matter. Sometimes, the most profound lessons about life come from the most unexpected places. Many of us are doing it tough in the current economical situation, but no matter how tough it is for us, it doesn't compare to what this little boy and his family is going through and will have to go through in the future. I urge you to look into your hearts and know that your assistance, however small, is contributing to give him a slightly better quality of life. https://lnkd.in/gURn3UGm #childhoodcancer #cancerawareness #cancersupport #fightcancer #cancercommunity #cancerwarrior #donatenow #supportkids #giveback #makingadifference #gofundme #fundraising #togetherwecan #childhoodcancerawareness

CHANGING THE WAY MEN GO THROUGH CANCER Man Up to Cancer inspires men to connect and avoid isolation during their cancer journeys. As North America’s leading support community for men impacted by cancer, we offer peer-to-peer support, an annual retreat, chemo backpack program, learning opportunities, and more than 30 local chapters geared toward improving the quality of life of our members. When faced with cancer, women tend to “reach out,” and men tend to “check out.” This leads men down the path toward mental health problems, strained relationships, and poor medical outcomes. It’s time for a new path. We are changing what it means to “Man Up.” It’s not just about being tough. It means having the courage to accept help, and knowing we are smarter and stronger as a pack than we are as lone wolves. As one who was not in a good place dealing with my own cancer journey. Man Up To Cancer was part of me growing and dealing with this cursed disease. If you plan on giving, please consider #ManUpToCancer. https://lnkd.in/giJqa7Rk

Pinky Swear Foundation helps kids with cancer and their families with financial and emotional support. You can make a difference. Your gift helps families focus on what matters most - their child. Learn more about the Pinky Swear Foundation and ways to give below. #PassItOn

Time really does fly! In 2023, I was the RARE KNIGHT! Organized by Avanzanite Bioscience, standing before biotech executives, investors, advisors, and #raredisease advocates, I found myself in a room filled with individuals passionate about making a difference in the realm of rare diseases, in my case #acanthamoebakeratitis. It was an incredible and somewhat humbling experience to share the #patientsperspective on the impact of this rare disease both during and after. I will forever appreciate being giving this title, as well as the support towards our mission at the Acanthamoeba Keratitis Eye Foundation. It is time to show support for #Nephrokids, who are dedicated to addressing #chronickidneydisease. Only those who have experienced this disease firsthand or witnessed a loved one struggle with it can truly grasp its impact. Here is another remarkable #raredisease #foundation established by individuals who have directly experienced the patient's perspective and are eager to make a positive change. Attending the #event or making a #donation can truly have a significant impact! #fundraising #makingadifference #charity, #orphandrugs, #patientadvocacy, #nephrologist, #paediatric,  #nephrologie, #biotech, #community, #kindernephrologie,

‼️I don’t normally make posts like this on LinkedIn but this is something which is very close to my heart. I want to make use of my network here to raise awareness for the issue and also raise funds for the various charities who have helped us along the way. My husband, Venkatesh Hariharan, was diagnosed with Glioblastoma Multiforme (GBM) in 2022. He underwent multiple surgeries, as well as various chemo/radio. By June 2023, all our options were exhausted. He continued to remain active, carrying out his hobbies such as gardening and long walks as best as he could, spreading joy until the end of 2023. His condition started to decline from January 2024 onwards. He lost his battle on Tuesday, March 12th, exactly a week ago. GBM is one of the most aggressive brain tumours, accounting for 50% of all brain tumours. There are currently no treatments or cures for this type of tumour worldwide, and the average survival rate is only 12-15 months. As well as being a life-threatening, incurable cancer, GBM has devastating effects on brain functions, meaning the individual loses their cognitive & physical abilities, plus their independence and personality. GBM can affect anyone, and has no specific cause, which means that medical organisations and research centres need more funding to prevent this disease from affecting more lives. I have one key takeaway that I would like to share from this experience. Whilst science has yet to have found a cause for this dreadful disease, there are a few things that are within our control. Prioritise family, health and quality of life above all else. Our current culture is so work-centred, which can cause immense levels of stress and pressure to build on our brains. Don’t constantly chase numbers: targets are set every year and this number will keep increasing. Prioritise what matters to you most in life and make sure you keep this within sight. Maintain perspective, as our day-to-day stresses of work and numbers don’t matter in the grand scheme of things. Funding and donations are so important for GBM research. As part of this post, I would like to express my gratitude to: 1. Woking & Sam Beare Hospice and Wellbeing Care which provides end-of-life care. They were absolutely incredible and they are all true angels in disguise. My husband spent the last 4 days of his life in Woking Hospice and they were brilliant, beyond what I can write into words. We as a family are raising funds for Woking Hospice in my husband’s memorial page: https://lnkd.in/eKuUpdZJ 2. All the doctors and staff members at the Royal Marsden Hospital who supported us during this journey. My daughter ran a half marathon to fundraise for their charity: https://lnkd.in/eYueXJ5F 3. The Brain Tumour Charity who are tirelessly trying to find a treatment for brain tumours including GBM where government funding is minimal. https://lnkd.in/eJ9EFpYH #glioblastoma