Last week, #TeamPCG had an amazing time at #CampCresentMoon!🌙 Huge shoutout to the Sickle Cell Disease Foundation for creating an unforgettable summer camp experience packed with education and fun activities for kids battling #sicklecelldisease. It was such a joy to meet these incredible young campers!💙🎉
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🧠💙 May is Stroke Awareness Month! Let's join together to support the Stroke Association in raising awareness about stroke and its impact. In this blog we talk about how a #LiveinCarer can be pivotal in a person’s post-stroke recovery. We shine a light on their prevention, recognition, and aftermath and here to help support through #liveincare https://lnkd.in/dfVviEXc
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Check out the interview below for more details on how we assisted Jess and Pete in creating their perfect wet room! 🌟
Global MND Awareness Day 🌟 We recently helped Jess and Pete create their perfect wet room. Pete was diagnosed with MND in 2022, and since then, Jess and Pete have been well-known around Exeter for raising awareness for motor neurone disease. Whether this is educating schools or talking on the BBC, they are doing a fantastic job of teaching others about the disease. Follow Pete's journey here: mindovermnd.co.uk For more information and support visit: www.mndassociation.org #mndawareness #constructioncompany #refurbishment #exeter F-tec Building Services
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Saying ‘Yes to the Mess’- The Community Navigator 🗺️ Charity Consultancy Services🧭 - supporting organisations to make visions a reality, maximise impact & change lives! hannah@thecommunitynavigator.co.uk 07973864454
Growing up in the North Rugby League was in my blood, I remember pestering my dad for months to let me go watch his beloved Hull FC at the Boulevard Ground. The minute I stepped in I was captivated, the rickety old turnstiles, the paint chipped from the terraces and lush green grass got me hooked - I had found my church ⛪ ! But what I loved the most was how much people loved the game, not just their own team but an admiration for up and coming talent on both sides, exceptional ball handling skills or a 40:20 kick on the last.... it was heady stuff. But the biggest love of all was that Rugby League was a community itself, part of the fabric of northern life, woven invisibly into conversations at Sunday Lunch, at the core of factory work banter or analysed kick by kick- pass by pass in the pub. As it was announced last night that the incredible Rob Burrow had passed away, it got me thinking about how Rob's journey with MND. Not only did it showcase the incredible strength of the Rugby League Community but the resilience of the man himself - his values and his approach we could all learn so much from. Love: Loving what you do, the people in your life - it matters immensely. Life is precious and far too short to filling your time with the stuff that you do not enjoy. I know it sounds simple, but be conscious in your decision making and really as yourself is this something that I love? 😍 Friendship : In life we all need allies, the people who will be part of our troop - create the space safes to be our authenticate self and keep picking us up when we are rock bottom and celebrating your success. Rob's relationship with Kevin Sinfield has been widely publicised, but only true friends would do what Kev did for Rob 💓 Taking the Path of Most Resistance 🏔: Sometimes taking the easiest route out of a problem or overcoming a challenge feels like an appealing option. But to break new ground, to achieve greatest impact the hard stuff wins. There is no doubt in my mind that Rob lived 5 years post diagnosis by not taking the easy option. Creating a Burning Platform 🔥: When Rob was diagnosed with MND he was determined with use it for a force of good, raising millions of £ to aid better research, campaigning and services for people diagnosed with Motor Neurone Disease I will certainly be keeping this in my mind when working with The Community Navigator 🗺 clients this week... So next time you feel you need to mix things up lets chat.... lets all be a little bit more Rob! Sending lots of love to the Burrow Family and the wider Rugby League Community 💙 💛
We’re deeply saddened to learn of the death of our patron Rob Burrow CBE. Rob lived with motor neurone disease in the public eye after choosing to announce his diagnosis in 2019. We will be forever grateful to Rob. Sharing his journey with this disease inspired so many people both within the MND community and the wider public. Our thoughts today are with Rob’s wife Lindsey, children Macy, Maya and Jackson, family, friends and the rugby league community.
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May is Stroke Awareness Month, and at NeuraSignal, we're dedicated to raising awareness about stroke prevention and treatment. Together, let's spread the word about the importance of early detection, rapid response, and ongoing support for stroke survivors. #StrokeAwarenessMonth #NeuraSignal #HealthAwareness 💙🧠
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Motor Neuron Diseases are a group of neuro degenerative conditions that affect the voluntary control of muscle movement. However early symptoms can include: - weakness in your ankles or legs e.g. you might trip, or find it harder to climb stairs - slurred speech, which may develop into difficulty swallowing some foods - weakening of grip e.g. you might drop things, or find it hard to open jars or do up buttons - muscle cramps and twitches - weight loss e.g. your arms or leg muscles may have become thinner over time - difficulty controlling emotions e.g. crying or laughing inappropriately MND is uncommon, and while it can affect anyone, it is more common after the age of 60 years. However if you display any of the concerning symptoms above, then please consult with a doctor. CAS Medical has access to private neurologists across central Scotland, who specialise in MND. If you wish to arrange a consultation, then please email info@casmedical.org #casmedical #MND #motorneurondisease #privateGP #earlydetection
We’re deeply saddened to learn of the death of our patron Rob Burrow CBE. Rob lived with motor neurone disease in the public eye after choosing to announce his diagnosis in 2019. We will be forever grateful to Rob. Sharing his journey with this disease inspired so many people both within the MND community and the wider public. Our thoughts today are with Rob’s wife Lindsey, children Macy, Maya and Jackson, family, friends and the rugby league community.
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Parvo is Poop. Literally. Although parvo strikes throughout the year, today marks the beginning of parvo season, with late spring and early summer being the most common seasons for parvo outbreaks, spread mainly through contaminated dog feces. Defeating this deadly disease requires us to be innovative and bold. To help spread awareness and education around this deadly disease, join us as we recognize National Parvo Awareness Day to help Defend Puppies. Defeat Parvo. Learn more at https://bit.ly/3w5AyCl #DefeatParvo #WeAreElanco #NationalParvoAwarenessDay
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Doctor of Pharmacy | Pharmacovigilance | Patient Safety | Drug Safety | Regulatory Affairs. **All of my posts are personal and do not represent the position of my employer.**
Parvovirus, often simply known as parvo, is more than just a disease—it's a critical threat to puppies and dogs, especially during its peak season starting now in late spring and early summer. Parvo is primarily spread through contaminated dog feces, making today a vital reminder for all pet owners and animal lovers to take action. As we step into what's commonly known as parvo season, it’s essential to highlight the seriousness of this highly contagious virus. It's not just about keeping our neighborhoods clean; it’s about saving lives and preventing the spread of this deadly disease. By joining forces on National Parvo Awareness Day, we can Defend Puppies and Defeat Parvo through increased awareness and education. Be bold, be innovative, and join us in the fight against parvo. Learn more about how you can help make a difference today 👉 https://lnkd.in/eKCqGknK Let's spread the word, not the virus! 🐶 🐩 🐕 #ParvoAwarenessDay #DefendPuppies #DefeatParvo
Parvo is Poop. Literally. Although parvo strikes throughout the year, today marks the beginning of parvo season, with late spring and early summer being the most common seasons for parvo outbreaks, spread mainly through contaminated dog feces. Defeating this deadly disease requires us to be innovative and bold. To help spread awareness and education around this deadly disease, join us as we recognize National Parvo Awareness Day to help Defend Puppies. Defeat Parvo. Learn more at https://bit.ly/3w5AyCl #DefeatParvo #WeAreElanco #NationalParvoAwarenessDay
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Today marks Fibrodysplasia Ossificans Progressiva (FOP) Awareness Day! 💙 Carli Lyn, a courageous FOP warrior, shares her personal journey living with an ultra-rare disease. She sheds light on the challenges she faces and the resources that have brought some relief to her daily life. Let's advocate for all FOP warriors, not just today, but every single day. 🦓 Go to TheBalancingAct.com/Rare to learn more about FOP. #BehindTheMystery #FOPAwareness #RareDisease #FibrodysplasiaOssificansProgressiva #RareDiseaseAwareness
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Psoriatic disease impacts not just individuals but also their loved ones. In this video, IFPA Ambassador Chiara shares her journey and how her family's support has been crucial in her experience. 💡 Watch the full film, 'Psoriatic Disease and the Family: Navigating Challenges Together,' to learn more about the impact of this disease on families. - https://lnkd.in/d7R-zwHN 🌍 Be a part of the change! Visit psoriasisday.org to participate in WPD 2024 and help raise awareness. #psoriaticdiseaseandfamily #WorldPsoriasisDay2024 #WPD2024 #Psoriaticdisease #psoriaticarthritis
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It is Skin Cancer Awareness Month. Outdoor workers, including those in construction, agriculture, and landscaping are at risk for sunburn and skin cancer. Train your employees about sun exposure, prevention, and first aid. Learn more: https://bit.ly/3fTYJHI
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