NF2 BioSolutions UK & Europe’s Post

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 #endNF2 #NF2awareness #neurofibromatosistype2 #NF2SWN #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 #endNF2 #NF2awareness #neurofibromatosistype2 #NF2SWN #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 #endNF2 #NF2awareness #neurofibromatosistype2 #NF2SWN #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 #endNF2 #NF2awareness #neurofibromatosistype2 #NF2SWN #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

In 14 days the LSP USA team will be running a 10K in support of HETEROTAXY CONNECTION . We would love your support by helping us reach our goal by donating to our GoFundMe (link below). 🏃♀️ For those of you who don't know, Heterotaxy is a congenital condition that disrupts the normal left-right asymmetry of the body. This can result in any of the internal organs being misplaced, malformed, multiplied, or missing entirely. The cause of Heterotaxy is not fully understood; some genetic links are being explored, but not all cases have been found to have a genetic cause, so research is still needed. Individuals with Heterotaxy require lifelong multidisciplinary care and medical monitoring. #10K #heterotaxyawareness #bringawareness #donate #fundraiser #LSPrenewables

If you are not yet aware of how #alkpositive #lungcancer can impact your world, please learn more about David Cornbrooks' story and his incredible #SweatForBreath effort to save lives.

Tis’ the season of giving!🎄This year Maxio has partnered with G2 Gives and the National MS Society to make a difference. For each review written on Maxio, G2 is donating $10 to support the fight against multiple sclerosis. The MS Society is near and dear to our hearts. Our CEO, Randy Wootton, is a longtime supporter of The National MS Society. He regularly participates in Society events and encourages all Maxio employees to get involved as well. 📝 Write a review now: https://lnkd.in/gfAn_QYw Multiple Sclerosis is an unpredictable disease that impacts the central nervous system. The National MS Society is dedicated to creating a world free of MS by helping those affected live their best lives, stopping MS in its tracks, restoring what has been lost, and ultimately ending MS forever. #G2 #G2Gives #NationalMSSociety #MSSociety #seasonofgiving #subscriptionbilling #subscriptionanalytics #subscriptionrevenuemanagement #billing #subscriptionmanagement

Why are we interested and focusing on RAi1? Past research into Smith-Magenis Syndrome suggests that correcting the dose of RAi1 cannot only be beneficial for those with the syndrome but in some instances may reverse some symptoms. We believe this may be the case for PTLS as well and are working to further research here. If you are interested in helping fund this research- consider donating to our cause. 💚

What are common myths surrounding living liver and kidney donation? Candice Coghlan, Education and Outreach Coordinator at the Centre for Living Organ Donation gives you an insight into the common myths surrouding living organ donation. Want to learn more about the Centre for Living Organ Donation and how to become a living donor? Visit livingorgandonation.ca #kidneydonation #livingorgandonation #livingdonor #beadonor #showyourscar #commonmyths #mythorfact #resources #centreforlivingorgandonation #organ #donate #givelifeuhn

❓Can we raise 5.000 kr together for Cykelnerven / Scleroseforeningen with this post? ❓ If you see this post, I challenge you to support my fundraiser with 10kr. It’s easy and rewarding. Link in the comments. — I have an issue with my fundraiser for Cykelnerven / Scleroseforeningen this year - not a single donation so far 😢 Every penny travels uncut to R&D and real help for the ones living with sclerosis. I’ve had between 1.000 and 2.000 impressions on my fundraiser posts recently. If just 500 people donated 10kr we would have reached 5.000kr. 1 in 350 people are diagnosed with MS in Denmark, that’s 8.5x the rest of the world average 😱 We have no clue why. How creepy is that? That’s one of the reasons we need to raise funds for this cause - for a world without MS. Even small contributions make a big difference.