Employee Foundation of the VKR Group’s Post

As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Oscar. His NF2 journey started aged 6. "Oscar has a juvenile cataract in his left eye and a very low level hearing loss. He is an NF2 warrior and born a fighter. 13 months ago he underwent major foot surgery due to mobility problems caused by spine tumours and has Avastin infusions which are every 4 weeks to control his tumours. He is a football player and shares a passion for Nottingham Forest with most of his oncology team!" NF2, is a lifelong genetic condition, There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. There is no cure, Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Kim Whitlock who says "NF2 can be a daily battle. Physically I have mobility difficulties, SSD, facial paralysis & dizziness. But the psychological side can be more disabling. There's been times where I've fought daily battles with anxiety & depression. But NF2 has also made me a positive person & I try to prioritise myself & my health" NF2, is a lifelong genetic condition, There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

Topic: Dislocated IOL That’s not supposed to be there! Today’s case was submitted by Anjana Mirajkar (@anjanamirajkar) and Manish Nagpal (@drmanishnagpal). This patient presented with a spontaneously posteriorly dislocated intraocular lens (IOL). The lens was explanted, and a secondary scleral fixated lens was placed. Unfortunately, we don’t have any further clinical information. Go to www.retinarocks.org/cases for more dislocated IOL cases. [This case can be found on www.retinarocks.org in the Image Gallery, Cataract + IOL folder, Dislocated IOL MN1-20240608] Have an interesting case and want to help your peers learn something about the retina? Submit your images at www.retinarocks.org. Retina Rocks and its charitable foundation, "Eye Reach" are supported in part by Optos (@optomap) and Topcon Healthcare (@topconhealthcare). Retina Rocks is the image bank for the Retina World Congress (@RetinaWorldCongress). #dislocatediol #retina #optometry #ophthalmology #cool #odsonfacebook #adarshcharitablefoundation #UWF #optos #optomap #TopconHealthcare #savingsightsavinglives #RetinaWorldCongress

As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet James whose NF2 journey started in 2021, he is now 57. He explains why its important for us to talk about NF2 so we are able to cope mentally as well as physically. "I struggle mentally sometimes to cope with my balance and hearing and get really annoyed with myself but try to stay positive and focus on what I can achieve" NF2, is a lifelong genetic condition, There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion.. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

NF2 can be a daily battle. Physically, mentally and emotionally. But the psychological side can be more disabling. Daily battles with anxiety & depression. Help us #ENDNF2

🌟 Join the Movement Towards Sports Excellence and Joint Health with CAO Research Foundation! 🌟 In the world of sports, the pursuit of excellence often comes with a price: the risk of injury and the specter of arthritis. The CAO Research Foundation is dedicated to changing this narrative, ensuring that athletes and individuals of all levels can pursue their passions without fear of debilitating joint issues. Picture a future where anyone can push their limits without the fear of injury or arthritis slowing them down. With your support, we can make this a reality. Every contribution to the CAO Research Foundation drives us closer to innovative solutions. From studying the impact of sports on joint health to developing advanced treatments for arthritis, our research is paving the way for a future where sports and orthopaedics go hand in hand. Join us in this transformative journey. Your donation is not just an investment in research; it's a commitment to the well-being of individuals everywhere. Together, we can rewrite the playbook on orthopaedic issues and give mobility and relief of pain to patients. Be a part of the change. Support CAO Research Foundation today! 🏃♂️🔬💪 #CAORF #JointHealth #SportsExcellence #Innovation #Orthopaedics #DonateNow https://lnkd.in/ez8wPqu9

Personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. #ENDNF2

March is Women’s History Month! It’s also Endometriosis Awareness Month! For those who don’t know, Endometriosis is a debilitating disease in which uterine-like tissues grow out of place and become inflamed during a woman's menstrual cycle even though the tissues are outside the uterus. The symptoms are varied and brutal, often causing high levels of pain and psychological distress. You might think it’s rare, you’d be wrong. It affects a whopping 1 in 10 women. Surely, our healthcare system is equipped to deal with such a disease, you’d ask. You’d be wrong again. The worst part of endometriosis is that it can take on average 7-8 years to get a correct diagnosis. 7-8 years to be told there’s no cure, only pain mangement and surgery. Thankfully, good folks like Endometriosis UK are working hard to bring awareness to all and support to the many women affliced by this terrible disease. That is why for the entire month of April (due to travels in March) I will be cycling a minimum of 1,000 km to raise £3,500 for Endometriosis UK. Every little counts and if you’re reading this and feel compelled to donate, you can do so below! Together, we can ensure those with endometriosis receive the care and support they need and deserve.

As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Hannah, her NF2 journey started aged 14. Hannah has suffered severe, life changing side effects from Avastin infusions. " So far, I’ve had yearly MRIs since I was 14. Countless injections, bloods taken, eye, ear tests, Hormone treatments more needles… and now finally Avastin treatment so I can keep my tumours small so I can keep my hearing for a bit longer. Avastin makes me tired and sick" NF2, is a lifelong genetic condition, Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research at https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2

As we approach NF2 Awareness Day on May 22, it’s heartwarming to see the efforts to raise awareness and support research for this condition. Real people affected by NF2 are sharing their journeys, shedding light on the challenges they face, and inspiring hope for better understanding and treatments. These personal stories serve as powerful reminders of resilience, courage, and the importance of community. By sharing their experiences, these individuals contribute to a collective effort to improve the lives of NF2 patients and their families. We are each affected differently & people with NF2 are affected by Brain Tumours, Spine Tumours, Optical Tumours, Deafness, Blindness, Epilepsy, vocal chord paralysis, mobility problems, chronic pain, cataracts, facial palsy ... & much more! Today we meet Aimee who is 41 and has had numerous surgeries to her brain and spine but still tries to remain positive about life with NF2. NF2, is a lifelong genetic condition, that weaves itself into the fabric of existence, unyielding and unrelenting. There is no middle or ending to any of our stories. Surgery, radiosurgery, and chemotherapy—are the only options we have. Yet, they come at a cost. Their impact reverberates through the delicate pathways of nerves, often leaving behind scars of lost function. NF2 is for life, an unwavering companion. It defies the boundaries of time, refusing to be confined to mere moments. There is no cure, no magic elixir to erase its presence. Instead, there is resilience, determination, and a shared journey among those who navigate its complexities Please consider donating to research, sharing your story & raising awareness. You can donate here to our research https://lnkd.in/euWUGuTS #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2