PureGym’s Post

Did you know that for the nearly 1 million people with MS in the U.S., the average total cost of living with MS is $88,487 per year? Not only is the National MS Society funding research towards a cure. But we also work to improve access to personalized, affordable, high-quality MS healthcare. You can make a difference this week by donating here- https://lnkd.in/eRFJmmBk #bikems #fundraisingweek

Wonderful progress by our innovative charity with an accelerating number of partners. Our technology and analytics capabilities accelerate medical research, help patients and clinicians with healthcare, rare disease, and unexplained symptoms. New insights are being achieved for healthcare services with significant benefits in reduced cost and speed. #ourfuturehealthuk #innovation #futurism #clinicalresearch #lifesciences #pharma #healthtechnology #digitalhealthcare #royalsocietyofmedicine #clinicalinformatics #analytics

Together, we can make a life-changing impact. Spread awareness about organ donation and help save lives. #organdonation #donatelife #organdonationawareness #kidneytransplant #kidneydisease #organdonationsaveslives #transplant #duticorp #digitalmarketing #agency

Rest assured, if you use our services - we will hear you.💚 Therapy can feel terribly daunting and the fear of not being listened to, believed, or even that your problems aren't "bad enough" are very common. Your feelings are valid. If you need help, get in touch: https://buff.ly/30SwZfp #ChestersMentalHealthCharity #MentalHealthAwareness #Charity #ItsWhatWeDo #Chester #ChangingLivesForGood

Abe's parents share what life is like for Abe & why #TeamAbe are doing a 100km walk for EB later this month. https://cure-eb.org/press/ Cure EB is a research-focused charity, dedicated to finding effective treatments and a cure for all types of Epidermolysis Bullosa. #CureEB #ResearchtheCure #EpidermolysisBullosa

Ending human trafficking requires all of us to stand together. Let’s unite our voices, actions, and hearts to create a world where every person is free. Together, we can make a difference! You can also make a difference by becoming a PPP partner and funding our organization. Please click on link in bio and select Donate! #endhumantrafficking #standtogether #raiseawareness #donate #support #humantraffickingawareness

Tips for how to get involved from someone who knows. 😊 We love our board members because sharing is caring when it comes to getting more kids on bikes. Donate by clicking the link 👈 Share this post with your followers ❤️🧡 #morekidsonbikes #education #bicycle #healthy #mentalhealth #nonprofit #donate

"I'm a big believer that if you live in the community you should give to the community." - Adam Gill, 2023 CAN GIVE DAY Big Wig Challenger 🦾 🏥 Our Big Wigs may be in competition, but they all have one thing in common - they are passionate about making a real difference in the lives of those living in Canberra and the surrounding regions. 🏗️To abseil down a building, our Big Wigs must first raise an entry fee of $10,000. These funds directly enhance the healthcare experience for patients and families in Canberra and the surrounding region. 💰 =💰💰 You can help our Big Wigs help our community. Donating today will double your impact; every $1 you donate to a Big Wig will become $2. Which Big Wig will you choose? https://bit.ly/4910jT4

The team at Nu Image Ltd are soon to take part in a 24hr cycle, outside the front of our Norwich studio to raise much needed funds for Endometriosis UK - in short we would love your support. So please... 1. 💷 Donate here - https://lnkd.in/eEQpfTCA 2. 🚲 Come and join in, using our guest bike 3. 💌 Share this post Or secure the hat-trick and go for all three. _______ If you are interested in why the guys have picked this charity in particular, here is some insight into my story... I have suffered with Endometriosis for many years now, and to be frank it sucks. It slows up my ability to function fully day to day, both physically and mentally. For the most part, I tend to keep it under wraps and tucked away from my professional life, just like many other woman who are also dealing with it. I was told that the team at Nu would be undertaking this challenge, after they had already secretly organised it…I'm looking at you Ian Howes, likely because they thought I would stop them doing it for me. I was touched that they were so committed to support me (love them), and the cause BUT I won’t be stopping them because this isn’t just about me. It is WAY bigger than that. As a condition Endometriosis is rarely talked about and diagnosis times are unacceptably high. I waited around 6 years to be diagnosed, by which time I was carrying around several large cysts on my ovaries, one the size of a tennis ball, despite raising Endo as a possibility during assessments more than once, as my mum also suffered from it. I have undergone major surgery and still the condition continues to grow, even as far as my diaphragm, meaning I have more surgery to come, with higher risks this time. Unfortunately, that’s a frustratingly common outcome, with the average diagnosis time being 8 years. Often by the time patients are offered help, the extent of the spread can be impossible to reverse. Endometriosis is debilitating, it is responsible for chronic pain and fatigue, depression and brain fog (very frustrating when you are trying to run a business!). It can also leave you with a difficulty/ inability to conceive, and yet is still not being taken as seriously as it deserves to be. Woman deserve more than this. Please donate and share if you can. Thank you.