#IntegratedCareSystems across England are made up of two parts: 1️⃣ Integrated care boards (ICBs) 2️⃣ Integrated care partnerships (ICPs) Watch our short animation to learn more about how these systems work across England. #KFExplain
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#IntegratedCareSystems across England are made up of two parts: 1️⃣ Integrated care boards (ICBs) 2️⃣ Integrated care partnerships (ICPs) Watch our short animation to learn more about how these systems work across England. #KFExplain
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#IntegratedCareSystems across England are made up of two parts: 1️⃣ Integrated care boards (ICBs) 2️⃣ Integrated care partnerships (ICPs) Watch our short animation to learn more about how these systems work across England. #KFExplain https://lnkd.in/d3_YCcAr
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#IntegratedCareSystems across England are made up of two parts: 1️⃣ Integrated care boards (ICBs) 2️⃣ Integrated care partnerships (ICPs) Watch our short animation to learn more about how these systems work across England. #KFExplain https://lnkd.in/ddghXhrJ
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Every 5 minutes someone is diagnosed with MS. This disease has no boundaries, is not discriminating....it can happen to anyone! We do #TheMay50K because it’s a global disease with limited awareness in certain parts of the world, but also within orgnisations there is a lot of misunderstanding. Education , awareness & understanding diet , exercise & good mental health are so important to cope with this condition! Since I came out as a patient and when I started talking about my MS, I got a lot of messages and questions from other patients all over the world. Often sad messages. The misunderstanding is one of our biggest enemies. Companies firing people who get the diagnose, applicants rejected when being honest about their condition and not getting the job....this is discrimination and shouldn't be happening. 70% of the MS patients live a normal life without to many symptoms, but due to the misunderstanding and little awareness companies think an MS patient will be a 'problem' instead of an added value. This misconception must change....therefore we, MS-patients, ambassadors, MS International Federation (MSIF), MS Research and other MS foundations use May as MS awareness month. Herewith a short animation that I hope you will watch. https://lnkd.in/e5jYxgRr Donating to support my challenge this month can be done here: https://lnkd.in/eCXtYAH3 https://lnkd.in/eNYVPxAD #awareness #ms #inclusion
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Every five minutes, someone – somewhere in the world – is diagnosed with multiple sclerosis (MS), an often misunderstood and debilitating disease affecting over 2.8 million people globally. Despite its prevalence, MS often takes months – or even years – to diagnosis. This is due to common barriers that delay early detection including lack of public awareness of MS symptoms and costly diagnostic tests. That’s why, this #WorldMSDay, I hope you’ll join me in showing support for all those who courageously navigate life with multiple sclerosis, as well as the many others who make up the inspiring MS community. At Sandoz, we are deeply committed to improving the quality of life of people living with MS by pioneering access to more affordable treatment options – and we know this starts with raising awareness of the many ways this condition affects individual and families. I encourage you to take a moment to watch the below animation created by the MS International Federation (MSIF). It is a powerful piece in which you’ll hear first-hand from those living with MS about their journey to diagnosis and treatment, and how they have been affected physically, financially and emotionally since. #MyMSDiagnosis
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This year, due to many things affecting the Epilepsy community, you might see more posts about things Epilepsy related than normal, but please just briefly look at each. Currently, S is the most pressing in the acronym that gives you a summary of what the multiple posts/messages/e-mails could cover: Transportation issues for people with Epilepsy Educating - pushing Seizure Safe Schools Act (or something like it, in PA it is called DOMinate Epilepsy- which is now in revision stages) requiring seizure first aid be taught in schools Advancing - new opportunities (Michael P. Laughlin Education Center, CDSMP, various virtual networking groups, VA Center of Excellence, and more) Medical coverage - continued effort to try to make anti-seizure medications, tests, and ambulance rides more affordable under various kinds of insurances Share Your Story (a movie should be coming out about this called Under The Lights.) https://lnkd.in/e-aAxC2C Under The Lights is in its final week of fundraising to hit it's startup plateau amount and is still a little short. They have donation incentives even at low amounts. I have donated to this cause to show the importance of sharing your story and raising Epilepsy Awareness. If you donate to this, let me know so I can thank you. #epilepsyawareness #shareyourstory #epilepsyinourlives #knowledgeispower #overcomingchallenges #fundraising #makeadifference #donate
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Caregiver Consultant at Alongside Caregiver Consulting, retired social worker, Podcast Host (Island Treasures) & Co-Host (Self-Caregiving Strategies Podcast)
Check out this new video to see how practical it is to step up and help a friend or neighbour who is caregiving! Modify actions… not just words!
Caregiving is hard. I'm here to make it easier. | Care-y Godmother/Caregiver Coach | Caregiving + Dementia Care Educator | Caregiver Advocacy Award Winner | Video + Commercial + Content Producer
"You need to take care of yourself" was a phrase I heard often as a 24/7 caregiver to mom who was living with young onset dementia. It added stress and shame to my constant flurry of feelings. It highlighted what I wasn't able to do even though I was doing SO MUCH. This content is based on my lived experience and the intention is to support other caregivers and relying on care as a tool for understanding and support. Hope it brings a smile and an a-ha 🧚🏽♂️ Thanks TELUS, Canadian Centre for Caregiving Excellence, & The Dementia Society of Ottawa and Renfrew County for your continued support of our work and the work YOU do for caregivers and those that depend on them across the country. https://lnkd.in/g3KuR8Su Co-created Jessica Fraser PAT HOLDEN Thanks to all the cast and crew - we love and appreciate you as per. #caregivers #dementia #thingsnottosay #caregiving #canada #respite #friendsofcaregivers
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Proven strategic communications leader skilled in bringing an organization's core values to life for its employees, stakeholders, and customers.
Dread
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Debunking Hospice Myths 🚫 Myth: Hospice is a 'Place'. 💡 Fact: A common misconception is that hospice is a physical building or 'Place'. Hospice is wherever your home is. It's about bringing compassionate care to the comfort of your surroundings. At Moments Hospice, we're here to support you wherever you call home. Let's redefine the way we think about hospice. #HospiceCare #ComprehensiveSupport #HospiceMyths #HospiceFacts
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To create an engaging game concept, there must be the right combination of entertainment, action and personality. Yet the difference between a good game and a great one can rest on the game’s voice and narration. Having the right voices can truly make or break a gamer's experience and contribute to a more engaging game. Finding the right voice can be easier said than done, especially with niche gaming content. Jackpocket, Iron Galaxy Studios, Epic Games are you aware that the World Voices Organization, the only global non-profit organization for the voice-over industry, has a FREE database for professional voice talent called Voiceover.biz? Our goal is to bring together talent seekers and vetted voice talent, in a way that provides value to everyone. Every voice actor listed on voiceover.biz has gone through our rigorous review process. This ensures only the best quality experience for everyone. #voiceactor #voicetalent #talentseeker #voiceover #narration #gaming
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Something as simple as a health and comfort kit can make a world of difference to a veteran facing hardships. It's more than items; it's a gesture of care and solidarity. See how you can help make a difference at DVNF.org/Health-Comfort #MoreThanAKit #DVNFSupport #TheDVNF
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Passionate about mental health
2moAlways worth a re-read