NF2 BioSolutions UK & Europe’s Post

Raising awareness for NF2 related Schwannomatosis is crucial to support those affected and to promote research and better treatments. Here are some ways you can help: * Participate in Awareness Campaigns: * Organize Events: Host events such as bake sales, coffee mornings, or charity runs to raise funds and awareness. You can also share information about NF2 on social media to reach a wider audience * Donate to research to help change the lives of those with NF2 * Educate Others: Share information about NF2 with your community, friends, and family. The more people know about the condition, the more support and understanding there will be. #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2 Reading real life stories about how NF2 affects people help others to understand why we need better treatments. Please help us to make that happen by donating to research, sharing your story & raising awareness.

Raising awareness for NF2 related Schwannomatosis is crucial to support those affected and to promote research and better treatments. Here are some ways you can help: * Participate in Awareness Campaigns: * Organize Events: Host events such as bake sales, coffee mornings, or charity runs to raise funds and awareness. You can also share information about NF2 on social media to reach a wider audience * Donate to research to help change the lives of those with NF2 * Educate Others: Share information about NF2 with your community, friends, and family. The more people know about the condition, the more support and understanding there will be. #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2 Reading real life stories about how NF2 affects people help others to understand why we need better treatments. Please help us to make that happen by donating to research, sharing your story & raising awareness.

Raising awareness for NF2 related Schwannomatosis is crucial to support those affected and to promote research and better treatments. Here are some ways you can help: * Participate in Awareness Campaigns: * Organize Events: Host events such as bake sales, coffee mornings, or charity runs to raise funds and awareness. You can also share information about NF2 on social media to reach a wider audience * Donate to research to help change the lives of those with NF2 * Educate Others: Share information about NF2 with your community, friends, and family. The more people know about the condition, the more support and understanding there will be. #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #strongertogetheragainstnf2 Reading real life stories about how NF2 affects people help others to understand why we need better treatments. Please help us to make that happen by donating to research, sharing your story & raising awareness.

Good news for faith-based organizations! According to a recent report from Givelify and The Lake Institute, 56% of faith-based givers responded that they intend to give more in 2024, while 42% expect to donate the same amount. Now might be the perfect time to start planning a campaign! If your faith-based organization is thinking of launching a campaign, reach out today to discuss how The Angeletti Group can help. Read the full report here: https://lnkd.in/eCzSwdRg #faithbasedfundraising #fundraisingtrends

Our main approach to increasing grant-funding success for researchers and charities is co-conceptualisation. We deep-profile the funder and the call, looking at their values as an organisation and their priorities within already-funded projects, as well as the published guidelines, so that we can help our clients better align their proposal by adjusting the plan of work to "tick all the boxes": we figure out precisely what the funder wants, and help you shape your concept around it. Once you've done that, it becomes hard for the funder to say "no".

Did you know that Talk Lipoedema is a registered charity? All the events and courses that we run rely on funding as well as donations from you. You can set up a regular donation or a one-off payment on our website: https://lnkd.in/eqazDZk2 Find out more about how we use donations to further the lipoedema cause on our website! #talklipoedema #charity #lipoedema #lipoedemacharity #lipoedemacommunity #lipoedemaawareness #lipalgia #lipedema #lipedemaawareness #lipedemacommunity

💙 Giving back feels good—and makes a real difference. Whether supporting disaster relief, funding medical expenses, or helping a loved one in need, every donation counts. 💡 In this blog, we share: - How to identify the causes that matter most to you - The impact of your donation - Tips to make your giving more meaningful 👉 Read the blog and start donating to causes you love today! https://lnkd.in/ecBxjh8P  #givingback #crowdfundingplatform #angelinkcommunity

Fundraising is vital so we can continue our research In the UK, about 1100 people are affected by NF2 (incl. 330 children). We need to ensure the physical and emotional wellbeing of those affected by NF2 without the need for invasive surgeries or treatments that may rob them of their nerve functions one at a time. A marathon; A bike ride; A cake sale; A birthday fundraiser; A coffee morning, A balloon race, A golf Day or even a virtual event ?...... Whatever you want to host, create your own fundraiser on the Peoples fundraising platform for NF2 BioSolutions UK. If you want help with ideas, then drop us an email. We have loads of resources to help make your event AMAZING too and you can loan our banner. Together we can give hope to those with NF2 and their families. #endNF2 #NF2awareness #charity #fundraising #donations #neurofibromatosistype2 #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #strongertogether #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #NF2SWN#nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #fundraising #charity

Did you know that the Reach Out & Read model has been supported by more than 15 independent and peer-reviewed research studies? This model works! DONATE: https://lnkd.in/djgBdy2 #Donate #reachoutandreadgny #readtogether

My platform Influential Stars has been created to raise awareness and funds for various causes in the UK, including charities and crowdfunding campaigns. However, the charities themselves don’t actively have to engage instead they simply just need to sit back and wait for their funds to come through. I’m reaching out to ask for a favour: please tag as many charities or crowdfunders as possible to let them know that if they have followers with over 10K on their platforms, they can contact them on behalf of Influential Stars and ask them to join and support their cause. That’s all they need to do! As a mum with an inoperable brain tumour, Officially Lisa Connell - I need help launching this platform, and that’s where I need your support 🙏 #HelpLisa2HelpOthers #TeamConnell #Charity #Charities #WinWin #Awareness #Funds