Melanoma Focus’ Post

As you probably know, black communities often face higher rates of blood diseases like sickle cell. But did you know Black donors, especially those with the Ro blood type, are critically needed to ensure the best possible care? Patients with blood disorders often need blood closely matched to their own ethnicity. Black people have a higher frequency of certain blood types critical for treating these conditions, like the Ro blood type. About 55% of black people have a Ro blood type, compared to 2% of the wider population. The Ro blood type is a variation of Rh positive blood, more common in Black individuals. For many Black patients with sickle cell disease, who often have the Ro blood type themselves, donations from Ro-positive Black donors are ideal for optimal transfusion compatibility, leading to better outcomes and fewer complications for patients with sickle cell disease. By donating blood, especially if you have Ro blood type, you directly help others within the Black community who may need it most. Every donation makes a difference! Join the community on BlackPharma.org #BlackPharma #BlackBloodMatters #DonateBlood #SickleCellAwareness

Crohn's disease, anxiety, dyslipidemia, prediabetes, and neutrophilic dermatosis, these are just a few of the comorbidities Kaleigh has developed due to her lifelong battle with psoriatic disease. Diagnosed at just 18 months old, Kaleigh has never known a life without psoriatic disease. Your gift to NPF will help continue to fund critical research into psoriatic disease comorbidities and deliver life changing resources to people like Kaleigh. Donate today and help those battling more than just psoriatic disease: https://ow.ly/10ye50QGgMj

October is #BreastCancerAwarenessMonth, a time to shine a light on this disease affecting millions worldwide. Let's empower ourselves and others by: 1. Knowing the signs: Be aware of changes in your breasts, like lumps, pain, or nipple discharge. 2. Getting regular screenings: Mammograms are crucial for early detection. 3. Supporting research: Donate to organizations working towards a cure. 4. Sharing your story: Your experience can inspire and uplift others. Together, we can make a difference. #CancerTreatment #Empowerment #HealthEducation #EarlyDetectionSavesLives #DrAaronWilliams #HealthyLifestyle #RaiseAwareness #CancerPrevention #WeeklyWellnessShow #BreastCancer

Recurrent hypoglycemia in newborns, infants, and children is not normal. To find out how you can help #StopTheLows, visit our website at the link in our bio to learn about our programs and donate to a #FutureWithoutLows 💙🩵⁠ #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia | Hyperinsulinism | Congenital | HI | Hypoglycemia | Rare Disease

Supporting Breast Cancer Awareness Month! Key reminders: Regular Screenings: Early detection saves lives. Know Your Risk: Understand family history and lifestyle factors. Healthy Habits: Eat well, exercise, and avoid smoking. Support and Speak Up: Encourage conversations and offer support to those affected. Get Involved: Donate, volunteer, or participate in awareness events. Let’s take action for better health and stronger communities! #BreastCancerAwareness #ThinkPink #EarlyDetectionSavesLives

Rare diseases like NF2 affect fewer than 200,000 people, but their impact is significant and often misunderstood. One of the challenges of rare diseases is that symptoms can vary widely from person to person, making diagnosis and treatment complex. NF2 is no exception. This genetic disorder causes tumors to grow on nerves throughout the body, leading to a range of symptoms, including hearing loss, balance problems, vision changes, and more. But here's the thing: no two individuals with NF2 are exactly alike. The symptoms they experience and their challenges can be unique to them. That's why raising awareness and supporting research is so crucial. With your help, we can better understand NF2, develop targeted treatments, and provide personalized care for those affected. Together, we can ensure that no one faces NF2 alone. Join us this Rare Disease Day in shining a light on NF2 and supporting our mission to find a cure. Every donation brings us closer to our goal and offers hope to those living with NF2. Click here to donate: https://buff.ly/4c35L9w https://buff.ly/3SWE6OD #RareDiseaseDay #NF2 #NF2Awareness #NeverForget2LivewithHope

Our Group Compliance Manager, Su Mawdsley is currently completing a challenge for the Motor Neurone Disease (MND) Association to raise funds in aid of combatting this cruel degenerative disease. As a cause close to Su’s heart, she has taken on the challenge of running a total of 60 miles by the end of August, a feat which Su has nearly completed! This is astonishing given that some years ago Su severely damaged her knee, subsequently undergoing surgery in April 2023, at which point, her consultant advised that she would never be able to run any distance again. In Su’s own words ‘I’m a stubborn individual who wasn’t going to take that lying down, so when the opportunity to take part in this challenge arose, I decided to put the 16 months of physio to the test!’ Su has asked if anyone reading would be kind enough to support her in this challenge to raise much needed funds. Any amount, no matter how big or small will go a long way to helping raise awareness of and find a cure for MND. THE DIFFERENCE YOU CAN MAKE   £10 could provide an information pack for someone newly diagnosed with MND. £20 could buy an LCD writing tablet to enable someone with MND to continue to communicate with their loved ones. £35 could buy a memory box for a child affected by MND, allowing families to capture memories that will provide comfort to the child in the future. £72 could pay for an MND researcher to use a high-powered microscope for 4 hours. £85 could pay for someone affected by MND to record their voice to be used to communicate when they are no longer able to. £200 could fund a Biozoon kit, allowing someone with MND who is unable to eat solid foods to continue to enjoy their favourite tastes through a dissolvable foam. https://lnkd.in/er4m-QhW

A snippet of our research..

Did you know that about 60% of babies with HI develop hypoglycemia within the first month of life? Hypoglycemia - critically low blood sugar - within newborns can cause seizures or permanent brain damage, amongst other complications. To find out how you can help #StopTheLows, visit our website at the link in our bio to learn about our programs and donate to a #FutureWithoutLows 💙🩵 #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia | Hyperinsulinism | Congenital | HI | Hypoglycemia | Rare Disease

Donate to Empower Stronger Lungs for Everyone! 🌟 Lung disease affects 1 in 5 Canadians, yet it's often overlooked and underfunded. We urgently need your help to support those struggling with lung health issues. 💙 Your donation is critical, especially for those facing a lung cancer diagnosis. With COPD projected to cost $9.45 billion annually by 2030 and 53% of COPD patients in long-term care, your support is vital. 👉 By standing with us, you actively combat COPD, the leading cause of hospitalizations in Canada, and work towards preventing the estimated 250 annual asthma-related deaths. Your generosity also addresses the concerning trend of youth vaping. 🌟 Your contribution is crucial in addressing the complex challenges of lung health in our nation. It fuels our mission, providing essential programs and services for those affected by lung issues. 🌈 Your gift supports initiatives like Fitness for Breath, our exercise maintenance program for those with chronic lung conditions. It's about transformation, community, and unwavering support. 💪 Donate now: https://lnkd.in/giDt2c8K #LungHealth #DonateForChange #BreatheStronger