Do your #neurodiverse initiatives include #dyspraxia? (Hint: they should) Learn more and donate to support the Dyspraxia Foundation USA https://lnkd.in/gCrTx3AS Image Description: Flyer-like image with muted color dots on an offwhite background. With the statistic "1 in 10 struggles with dyspraxia" Text underneath says "This neurological disorder often affects motor skills, but very few know what it does- or how it affects kids and adults." Dyspraxia Foundation USA logo and website www.dyspraxiaUSA.org
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Founder and pro bono CEO Women's Brain Foundation | MD|Neuroscientists| Board Member|Advisor| Women’s Health| Building and Accelerator
"Ask and it will be given to you; seek and you will find; knock and the door will be opened to you." M. 7:7-8 In gratitude to all those who donated via #TWINT or #Gofundme until now such as Dr. Vinay Kalia, Mara Fornaro, Vaclav 🧭 Sulista. Funds are needed it to support our INDEPENDENT research at Women's Brain Foundation. https://lnkd.in/ewgRxPVv A personal call to the LinkedIn community to share our campaign raising awareness about female brain vulnerability to diseases such as #alzheimer, #multiplesclerosi, #depression, #anxiety and #migrane. Sex and gender precision medicine is the right approach to find a solution. Powered by Ogilvy and Ogilvy Switzerland #brainhealth #womenhealth
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🧠 #Hyperekplexia is a rare, hereditary neurological condition which causes muscle rigidity, jerky movement and exaggerated startled reactions. 🔊 These reactions are often triggered by external stimuli such as unexpected lights, sudden sounds and movements. 📖 To find out more about the condition and the support we offer to those with #HereditaryHyperekplexia here at The Brain Charity, follow the link below 👇 https://lnkd.in/e9G3gse9
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🧠🌟 Celebrate the Neuro Community with Us! 🌟🧠 Join hands with The Neurological Alliance across the UK as we celebrate the incredible individuals, charities, not-for-profit organizations, and support networks during Brain Awareness Week this week (11–17 March 2024). Why It Matters: It's a time to honor the strength, resilience, and unity within the neurological community. Together, we raise awareness, share stories, and amplify the voices of those affected by neurological conditions. Have You Received Support? Has a person or organization provided you with invaluable support to navigate your neurological condition? Share your story! Let's shine a spotlight on the individuals and groups who make a meaningful difference in our lives. How You Can Participate: Share your gratitude: Tag the person or organization and share your appreciation. Spread awareness: Use #BrainAwarenessWeek to raise awareness and support. Join the conversation: Share your experiences and connect with others in the neuro community. 🌟 Let's Celebrate Unity, Strength, and Support! 🌟 #NeuroCommunity #BrainAwarenessWeek #SupportMatters 🧠💙
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Brain treatment doesn't just heal the brain, it heals lives. It restores lost dreams, mends broken relationships, and reignites the spark within. Change Your Brain Foundation knows that you're not stuck with the brain you have—you can make it better. Our dedication to scientific research is breaking the chains of traditional thinking. Transform lives—donate now to unlock the secrets of neuroimaging. Visit our website to donate today changeyourbrain.org. #mentalhealth #mentalhealthawareness #mentalhealthcare #endthestigma #breakthestigma
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What is your reason? We asked Keith why he is Running for Parkinson's WA in the HBF Run for a Reason and he said "The reason is twofold, firstly a friend offered me the following reason many, many years ago: Do it, whilst you can, when you can, before you can't. And if I'm going to do it, then at least also include those who can't anymore and perhaps benefit them in some way or another, by raising some much needed funding. Thanks Keith for making a difference! To register - click here https://loom.ly/0vUMDqI or to donate click here - https://loom.ly/qeQrEso #NotForProfit #PurposeForProfit #Community #Healthcare #NeurologicalNursing #Neurology #Research #ResearchOpportunities #YourStories #OurImpact #Neurodegenerative #MedicalResearch #parkinsons #parkinsonsawareness #parkinsonsdisease
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In less than 4 weeks I am running the Great South Run (10 miles) for Motor Neurone Disease (MND) Association 🏃🏼♀️. Motor neuron disease is a progressive neurodegenerative disorder that affects the motor neurons in the brain and spinal cord. Motor neurons are responsible for transmitting signals from the brain to the muscles throughout the body, enabling voluntary muscle movement. When these motor neurons degenerate and die, it leads to a loss of muscle control and function. So far I have raised £670. £500 could provide a tablet device with specialist communication software, allowing someone to communicate with loved ones. £750 could fund an MND expert researcher for a week. In the next 4 weeks I would love to reach £750. There is not yet a cure for MND so research is key!! If you haven’t already there is still time to donate, please click the link in the comments. Below is an infographic explaining MND and how it affects the body. #mnda #motorneuronedisease #fundraising #greatsouthrun
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TIX: https://lnkd.in/eAXcQwHy Drugs like MDMA and psilocybin are being ushered into mainstream medicine, promoted as miracle cures for a host of psychiatric woes. But as psychedelics come to be seen as treatments for various types of psychological suffering, we are overlooking one of their most precious offerings: the potential for play. Through play, the invisible landscapes of our inner lives merge with the visible world we all perceive in our own unique ways. When we play, we always play with someone or something: it’s always a relationship: an encounter. And in this, and so much more, play is the Marrow of our compassion. To not play? Well, the best word for that is alienation: the estrangement from our own power to summon life in ourselves and an estrangement from other living beings. To exist as if everything is same as it ever was, same as it ever was, same as it ever was. Join Dr. Ross Ellenhorn PhD, for an evening of play discussion on what Play can teach us about psychedelics. *A percentage of ticket proceeds will be donated to Cardea's non-profit The Furthur Fund.
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We are doing Run for a Reason to raise money for Parkinson’s WA. They help people with Parkinson’s, the nurses know about the latest medicines. They help people by answering questions if you are u sure about anything. Mummy finds it harder to go to work and harder to go to sleep, except for the afternoons and she gets shaky if she doesn’t take her medicine. She can’t do Run for a Reason this year as she just had a foot operation. next year we hope she can walk the course. Thanks Lottie for making a difference! To register - click here https://loom.ly/0vUMDqI or to donate click here - https://loom.ly/qeQrEso #NotForProfit #PurposeForProfit #Community #Healthcare #NeurologicalNursing #Neurology #Research #ResearchOpportunities #YourStories #OurImpact #Neurodegenerative #MedicalResearch #parkinsons #parkinsonsawareness #parkinsonsdisease
HBF Run for a Reason 2024
runforareason24.grassrootz.com
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I'm taking part in The May50k With only a couple of days and KMs left, support me as I smash out 150km in The May 50K to help raise funds to support life-changing research into the prevention, treatment and finding a cure for Multiple Sclerosis (MS). Any contribution, whether it be large or small, will help the fight against MS! Some facts about MS: * Over 33,300 Australians have MS and 3 out 4 of those are women. * MS is most commonly diagnosed between 20-40 years old. * 2.8 million people worldwide are living with MS. * Every 5 minutes someone, somewhere in the world is diagnosed with MS. * With sufficient funding, our researchers are 10 years away from stopping MS. https://lnkd.in/gHfcd8AX
Support my 150km challenge to leave MS behind!
themay50k.org
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Who do you shine your light for? Join the Alzheimer’s Association in raising awareness and sharing who you shine your light for during June - Alzheimer’s and Brain Awareness Month. Comment below or share this post! Ready to get even more involved in the fight to #ENDALZ? Register for #TheLongestDay and raise funds for care, support, and research. Learn more at alz.org/TLD.
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