Walk The Line is out at the Take Root Dance Parkinson’s Disease Expo today at Oakland University Rec Center from 9-2. This is a wonderful event for the PD community with free classes and resources available to attendees. Come check it out! For more info on Take Root and their Dance for Parkinson’s classes: www.takerootdance.com
Walk The Line’s Post
More Relevant Posts
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Following on from our recent webinar regarding PARKINSON'S DISEASE and HOUSING DESIGN, we have put together a helpful guide as to how best approach the creation of an accessible environment for your service user and their carer: https://hubs.li/Q02zZqY70
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Here's the PWR!Gym crew on World Parkinson's Day! Today, and every day, we invite you to join us and countless others in raising awareness of this life-changing disease, and how we're all working toward a world without PD. #WorldParkinsonsDay #ParkinsonsAwarenessMonth #ExerciseIsMedicine
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April is #ParkinsonsAwarenessMonth! We'd like to bring awareness to this complex disease and recognize those who are fighting the battle with it. Learn more from the #ParkinsonsFoundation https://buff.ly/2ULpfXj #ParkinsonsDisease #ABCsofPD #livingPD
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Making the world a better place starts by working to support and promote health, education and community wellbeing in the diverse places we call home around the world. In some places, support may mean helping communities affected by crisis or in other places it may mean proactively supporting disease awareness, access to screening and diagnostics or helping to build clinics to support people accessing treatment. Learn more about how we support communities around the world: https://viatr.is/3UXcCt4
Supporting Our Communities
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This video depicts the reality of heart diseases. Every loss of life is someone’s brother, parent, wife, friend or child. Young people are being robbed of their futures everyday, and the reality is devastating. We must stop these needless deaths, and most importantly we must stop them now. Please consider your workplace supporting Heart Research UK, we are working so hard to find life saving treatments, and we won’t stop, until there are no more deaths from heart diseases! #charityoftheyear #socialimpact #csr #lifesaving #partnerships #ESG #charity #charitypartnerships #heartdisease #workplacewellness
As part of our ‘Last Goodbye’ campaign, Ali shared his story of losing his younger brother Graham very suddenly, aged just 26. Graham was a gifted pianist, and a huge Manchester United fan. The last time Ali spoke to him, they were talking about going to the gym. Later that day, Ali’s brother died. Heart diseases don’t care about goodbyes. Together, we can give more people the chance to say ‘I love you’. To find out more about the campaign visit https://bit.ly/3NWhsnk This is Ali’s story
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K stands for knowledge! 📖 #ABCsOfPD The Parkinson’s Foundation is here to empower you with Parkinson’s disease information and resources. Today for Parkinson’s Awareness Month, deep dive into the PD topics that matter most to you at: Parkinson.org/PDLibrary
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The countdown is on for #RareDiseaseDay 2025! Watch this year's video below, and get ready to participate by finding events happening near you here ➡️ https://lnkd.in/e8KBUvki
And the day has arrived! It is now officially 100 days until #RareDiseaseDay! We are so excited to see how you will be making Rare Disease Day 2025 a special and memorable one. A heartfelt thank you to our 70+ national alliances who lead the campaign in their countries, inspiring and empowering local communities to take part. Let us know your plans in the comments and be sure to send your events in through our website to be shared with others. Let’s work together to generate real and lasting change in the world.
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Hi PHers! This is a quick nd easy survey. It took me less than 3 minutes to complete. Please take the time to help others who have done so much much to help the PH Community. #BreathtakingAwareness
YOUR VOICE MATTERS! How can PHAWARE GLOBAL ASSOCIATION better support, engage, and advocate for our Rare Disease Community? By sharing your thoughts through this quick survey, you can help us tailor our efforts to meet your needs and amplify our collective impact. https://lnkd.in/gPA3PK7G
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Please take a few minutes to learn about this devastating illness and spread awareness where you can….
📆 Mark your calendars: January 28 is #WorldLewyBodyDay! On this day, join Lewy Body International, a global network of #Lewybodydementia patient-advocacy organizations, in spreading awareness and increasing understanding of this little-known disease in your community. Share this post and visit https://ow.ly/3VvI50UCiv1 to learn more about Lewy and help others do the same.
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Today marks the start of #GaucherAwarenessMonth. Gaucher is a rare, progressive disease with symptoms that worsen over time. Yet, patients with type 1 Gaucher disease, the most common form, can experience diagnostic delays up to 10 years. It's important to highlight patient stories in rare disease, here's one. #rareispowerful #raredisease #findthezebra
As part of #GaucherAwarenessMonth, we’re shining a light on the resilient patients who live with this #RareDisease and the importance of having a community to lean on. For Jade, one of the most important aspects of living with and managing her type 1 Gaucher disease was finding other patients who faced similar challenges and understood her experience firsthand. Attending in-person events, specifically for those with Gaucher disease, helped her to truly feel a connection with the community and build her support network. This October, learn more about Gaucher disease, explore available resources and see how patients like Jade are creating supportive networks: https://lnkd.in/e9a9SmMr
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