Operator Relief Fund的动态

Hundreds of people are diagnosed with a Cavernoma, every year. 1 person in 625 in the UK has a brain Cavernoma without symptoms (asymptomatic) which equates to roughly 108,000 people – enough to fill a large football stadium. This annual event #cavernomaawareness helps to highlight the frequency of Cavernomas in society. A Cavernoma is made up of abnormal blood vessels, and can be found in the brain and/or spinal cord; they can measure from a few millimetres to several centimetres; can get bigger, but doesn't spread to other parts of the body; and is neither a tumour nor a compression, but a malformation of blood vessels. For advice and support go to: https://cavernoma.org.uk/ Care First 24 Ltd Cavernoma Alliance UK #cavernoma #brainhealth #brainhealthawareness #brainhealthmatters #healthybrain

Are you hysterical? Or are your health concerns routinely dismissed & ignored? Medical gaslighting occurs when healthcare professionals dismiss or trivialize a patient's symptoms, often leading to misdiagnosis or delayed treatment. Women, in particular, are disproportionately affected by this issue. Studies show that compared to men, women experience significantly longer wait times for diagnoses of critical conditions such as cancer and heart disease. Additionally, women are less likely to receive aggressive treatment for traumatic brain injuries and are often under-prescribed pain medications. This disparity not only underscores the prevalence of implicit biases in medical treatment but also highlights the urgent need for systemic changes within healthcare practices to ensure equitable and empathetic treatment for all patients. When you vote for your daughter, you're voting for her healthcare. You're voting for equal research, representation, and care for half our nation's population. You can learn more here: https://lnkd.in/ebiP-Guf?#voteforyourdaughter ?? NIH; Khan, Kianaat & Tariq, Noor & Majeed, Saima. (2024). Psychological Impact of Medical Gaslighting on Women: A Systematic Review. Journal of Professional & Applied Psychology. 5. 110-125. 10.52053/jpap.v5i1.249.; Women are calling out 'Medical gaslighting.' (2023, June). The New York Times. #WomensHealth?#MedicalGaslighting?#HealthcareBias?#hysteria?

The Neurological Alliance of Scotland are thrilled to unveil their latest comprehensive resource; "Information for Unpaid Carers and Professionals": an interactive guide aiming to provide vital support for unpaid carers of individuals with neurological conditions. The Neurological Alliance of Scotland understand the challenges faced by unpaid carers and the vital role they play in supporting their loved ones with neurological conditions. This resource aims to provide an overview of some of the most common neurological conditions and direct readers to our member charities that offer specialised support services. ?? Here's what our resource offers: 1. A-Z list of neurological conditions supported by our member charities. 2. General neurological therapy centers and support networks. 3. Alphabetical listing of local carer centers for region-specific assistance. 4. National Carer Organisations for additional support. 5. Links to further information and external resources. 6. Directory of our charity members for quick reference. ??Read here! https://ow.ly/6m9S50RgWpq #NeurologicalAllianceofScotland #SupportingCarers #NeurologicalCondition #UnpaidCarers

Dr Panna Muqit’s top tips for speaking to your GP about difficult MS symptoms. 1. Write it down. 2. Get ahead of the game – let your healthcare professional know what your appointment is about. 3. Bring someone with you. 4. Your GP is just the start of this journey. 5. Find the right GP to open up to. We know that some MS symptoms can be difficult to talk about. That’s why seven MS charities: MS Society, MS Together, MS Trust. MS-UK, Neuro Therapy Network, Overcoming MS and Shift.MS are working together to shatter the stigma. Join the conversation. Search or use the hashtag #MSUnfiltered for open, honest conversations about life with MS. You are not alone. #MS #MultipleSclerosis #MSCommunity #MSAwareness #MSWeek #MSAwarenessWeek

This SWAY presentation was a class assignment focused on the current concussion guidelines. Concussion management continues to be an evolving process. The 2023 Amsterdam Consensus Statement and 2024 NATA Bridge Statement served as the starting point for discussing if the current guidelines met the needs of a concussed patient. Key additions and limitations showed that while there have been advances since the Zurich guidelines, still more specific guidelines are necessary. The presentation ends with undervalued aspects of concussion management. The main two aspects are a multidisciplinary team approach and concussion rehabilitation. One individual in the multidisciplinary team who is left out until the end is the patient themselves. To increase compliance with a treatment plan and symptom reporting, patients should be involved at the very beginning. Concussion management is a complex task, but working together for the greatest good of our mutual patient benefits all parties.

As its Heart Failure Awareness Week I thought the time was right to let you know what I am planning to raise funds for the marvellous Pumping Marvellous Foundation to help them continue with their great work in raising awareness . If you have a minute or so please read the on to give you an idea of what i am doing and more importantly why. And if you are able please also consider making a donation to my just giving page https://lnkd.in/dArsb3Pz Mont Ventoux – 3 Ascents in a day 1 Mountain – 3 Roads up to the top – So why not do all 3 in 1 day That’s the plan – But Why? No, it’s not just because I like to ride a bike (and I strangely enjoy riding uphill) – Although that does make this a bit easier. I am doing this because I want to raise both Awareness of & Funds for a Fantastic Charity called Pumping Marvellous. Who are Pumping Marvellous and Why do you need to know about them? Pumping Marvellous are a great Charity who raise awareness of HEART FAILURE and support those living with it. Until a few years ago I was blissfully unaware of Heart Failure and the impact it has on people’s lives, that was until my Wife Corinne was diagnosed. At which point we became aware but still had no real idea of what it was and what it was and what it meant for us and Corinnes life moving forward. Without Pumping Marvellous it is fair to say that we would still be stumbling to understand, it is Pumping Marvellous and their community that has provided support guidance and factual literature that has helped us understand. For that reason, I want to, in return, help them by raising much raising much needed funds so they can continue and build on the great work they are doing, and hopefully share awareness so we all have better knowledge of Heart Failure and what it means to those living with it! That’s the Why, so now for a little bit about the What. Mont Ventouux is an Iconic French Mountain, famous for its moonscape summit, which has featured many times in the Tour de France. It also has 3 road options to get the top so to do all 3 in a single day seems like a good idea for a bit of a challenge. The Numbers are – Total Distance 135Km (3 ascents and 3 descents) Total m climbed 4,400m. Target time – less than 10 hours (hopefully – including time to fuel) ??

Multiple sclerosis affects more young people than any other neurological condition; including my best friend and sister. It's a lifelong disease and there's currently no cure. That's why I'm taking part in the 2024 Sydney MS Walk Run + Roll this May to raise vital funds and awareness for people living with MS. My goal is to raise $500 to help make support and services possible; I would love if you could help me make sure that no one faces MS alone. #mswalkrunroll #fundraising #multiplesclerosis https://lnkd.in/gU93pk_4?

Yesterday I moderated a panel for the Alzheimer Society of B.C. and it was incredible to see not only our brave panelists share their stories authentically but also the power of community in a person's life. We talked about how with the disease of Alzheimer's or dementia, how lonely it can get because your community can often withdraw from you, even as a caregiver. It is like your loved one or you make them so uncomfortable they act as though you no longer exist. The groups you may have belonged to before no longer welcome you or simply create too many challenges, you are asked to not attend (or no longer invited) family gatherings or no longer frequent businesses. It was heartbreaking to know you have to develop coping with loneliness in addition to ether the burden of living with the disease or knowing your loved one is slowly dying in front of you. Those moments of joy you find as you "walk the journey" can not be shared with anyone because they are afraid. While I think we were able to create some strategies for those in the session, it is the heartbreak of loneliness that really impacted me. Listening to how quickly people disappeared or openly removed themselves from their lives showed me how much humanity we are losing. But there is hope. You can make a difference by looking around you. as 1 in 3 people are touched by the disease. Who do you know that could use a break in their day by having a visit, what co-worker do you see carrying the burden of caregiving who might need just need to be seen for what they are carrying, how do you interact with customers who may be in the early on-set of the disease and need more patience? If all anyone learned in that session was to be patient, and as our panelists reminded them be a good human, then it was a success. If someone walked away knowing they were not alone in their journey, and will reach out to the society, then it was a success. If someone reads this post and decides to invest of their organization to support their local society then I have also made a difference. I have said many times over, we are lost without our community. Community comes in all forms. It is those we work with, those we see on our regular commute, those we interact with at our regular shops, those we pass by on the street, not just our family and friends. Build a community that supports all and really we will become a better place. Organizations who live their purpose and truly invest in community will always get my dollars and support. Where do you invest? Does building community show up in your organization in all you do? I know Deloitte is an organization demonstrating their purpose in how they show up, and it is why I choose to work there. A reminder, for those local to BC, please consider attending the breakfasttoremember.ca. and help support those trying to create community for people living with the disease.

All the latest news and features from Headway, including the therapeutic benefits of nature after brain injury, 'Amnesia and identity', 'Shopping without stress', and much more! https://lnkd.in/eKcnvXt2

?? Men's Health - Lets Talk about it! The statistics are alarming and shed light on important health issues affecting men globally. Approximately 10.8 million men are grappling with a prostate cancer diagnosis, emphasizing the significance of early detection and awareness. Additionally, testicular cancer stands out as the most prevalent cancer among young men, underscoring the need for regular screenings and education on prevention. Moreover, the stark reality of male suicide rates is distressing, with one man tragically losing his life to suicide every minute. This poignant statistic highlights the importance of mental health support and initiatives aimed at addressing the underlying factors contributing to these devastating outcomes. It's crucial to initiate conversations, raise awareness, and provide support systems to combat these challenges and work towards better health outcomes for men worldwide. Let's come together to advocate for proactive healthcare measures, destigmatize mental health discussions, and promote a culture of well-being for men in our communities. #MensHealth #Awareness #Support #Suicideprevention #Movember https://lnkd.in/gxBDvyX3