My advocacy for building a Myalgic Encephalomyelitis Community is so much more than a personal mission—it is a call to action for society at large. Through education, empathy, and empowerment, I am dedicated to making a difference in the lives of those affected by Myalgic Encephalomyelitis, advocating for a future where this condition is met with the seriousness and support it deserves.

Most importantly we will strive to offer a Myalgic Encephalomyelitis Community for Myalgic Encephalomyelitis sufferers as well as their families.

As a passionate advocate for Myalgic Encephalomyelitis (ME) a complex and debilitating condition, I am deeply committed to raising awareness about the complexities and overwhelming impact of this condition.

Living with Myalgic Encephalomyelitis as well as Chronic Illnesses such as Endometriosis, Steatohepatitis, and De Quervain’s Syndrome, has provided me with not only a firsthand understanding of life with these severe conditions but also a burning desire to bring about change and offer support for those afflicted as well as their families.

Dealing with Myalgic Encephalomyelitis presents me with daily challenges. These obstacles have fueled my dedication to spreading awareness within the Myalgic Encephalomyelitis community and to the public.

It is important to bridge the gap of understanding and empathy between those affected and the general public.

To make a difference, I am educating myself to utilise social media and digital platforms as a way to empower my voice for education, raising awareness and building a Myalgic Encephalomyelitis Community of sufferers and their families locally as well as around the world.

By utilising social media, you can make a real impact and drive positive change, advocacy and community building. Recognising the potential of these platforms to reach a wide and diverse audience, I initiated a dedicated YouTube channel.

Click here to see my YouTube Videos

Help is available

My own journey began with personal health challenges related to Myalgic Encephalomyelitis and Endometriosis. Recognizing a lack of empathy and understanding in society, I vowed to decided to become an advocate for change.

Over the years, I have engaged in numerous advocacy initiatives, created a supportive community platform, and have set myself up to become an influencer in the chronic illness arena.  By raising awareness our community has not only impacted individuals facing similar challenges but has also contributed to a broader dialogue about chronic illnesses in our society.

It’s time for change !

Building a community for people with Myalgic Encephalomyelitis (ME) that is run by individuals living with Myalgic Encephalomyelitis themselves holds immense potential for several compelling reasons:

Ownership and Leadership

By being led by individuals with Myalgic Encephalomyelitis, the community promotes a sense of ownership and leadership among its members.

This fosters a collaborative environment where everyone has a voice and can contribute to shaping the direction and initiatives of the community, ensuring that it remains relevant, inclusive, and responsive to the needs of its members

Why this is so important

A Myalgic Encephalomyelitis Community for people with Myalgic Encephalomyelitis that is run by individuals living with the condition has the potential to be a transformative force, offering support, empowerment, advocacy, and a sense of belonging to its members while also driving positive change in the broader understanding and treatment of Myalgic Encephalomyelitis.

 

Recent blogs

This journey taught me the power of resilience and I hope that by sharing my experiences good and bad I can raise awareness and offer support to those facing similar challenges.

Living with ME means fighting a silent, daily battle. This honest post explores the emotional, physical, and invisible toll of Myalgic Encephalomyelitis.
Robotic wheelchairs are transforming mobility for people with disabilities, offering smart technology, AI navigation, and new levels of independence. But the high cost keeps many from accessing these life-changing devices. This post explores both the promise and the barriers — and why we need to make this tech more accessible.
Looking for books that support, empower, and inform life with Myalgic Encephalomyelitis (ME/CFS)? Discover my top recommendations — from medical guides and personal memoirs to mental health must-reads. These titles helped me advocate for myself, understand my symptoms, and feel less alone. A must-read list for anyone navigating chronic illness.
Join me as I unbox a gorgeous PR package from Kitsch, featuring haircare and self-care essentials perfect for life with chronic illness. From satin pillowcases to the holy grail claw clip for thick hair, I share honest thoughts on how each item supports my daily routine living with Myalgic Encephalomyelitis. This heartfelt video blends unboxing, ASMR, and a behind-the-scenes look at my life as a disabled content creator.
Could something as simple as a cup of tea offer relief from chronic pain? In this post, we explore the research-backed benefits of peppermint and other herbal teas in managing symptoms of Myalgic Encephalomyelitis, Endometriosis, IBS, and more. Discover which teas help, how they work, and the traditional wisdom behind these natural remedies — plus a few personal stories and favourites along the way.
Dr Paul Hwang's latest ME/CFS research offers new hope for those living with chronic fatigue. Discover how his unexpected findings on mitochondria and the WASF3 protein could reshape our understanding of energy production in Myalgic Encephalomyelitis—and why this matters for millions still waiting to be heard.
A Disney-inspired cartoon-style illustration of a woman with long dark brown hair and bright blue eyes lying on a bed, smiling warmly at two black Labradors wearing red collars. One dog has a tag labeled "Alfie," and both appear happy and content

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