🛑 Content Warning: Online Abuse, Ableism, Disability SlursThis video contains references to ableist language, online hate, and the failure of systems to protect disabled people. Please take care while watching.🎙️ This is a spoken word piece from my podcast Wheelie MS Advocate. It’s about what it feels like to live through constant digital ableism, on TikTok, X (formerly Twitter), and beyond.📍 Despite reporting the hate to the police, I was told nothing could be done. Why? Because the people abusing me aren’t in the UK.💬 But the abuse still landed here. On my screen. In my body. In my life.🧠 We are disabled — not stupid.We’ve had careers, built lives, and we still work — even when it breaks us.We don’t need more “coping tips.”We need protection. Real, global, legal protection.✊🏽 Stop calling us strong if you won’t stand with us.—🔗 Read the full blog post:👉 Wheelie MS Advocate📲 Follow me:TikTok: @wheelieMSadvocate_X/Twitter: @wheelieFUMSInstagram: @wheelieMSadvocate📧 Want to work with me or support my content?Visit: About me#DisabilityAdvocate #Ableism #HateCrime #OnlineAbuse #WheelieMSAdvocate #DisabledAndProud #AmbulatoryWheelchairUser #SpokenWord

“Disabled people are better off on benefits.”
That’s what the Daily Mail claims — again. But what’s the real cost of headlines like this?

In this solo episode of Wheelie MS Advocate, I share my lived experience as a disabled person on Universal Credit and PIP.

From public judgement to online abuse, from policy decisions to being labelled a “#SickFluencer,” this is what it really feels like to be the scapegoat in a political game.

🎧 Topics covered in this episode:

• How headlines fuel stigma and hate

• Why “sickfluencers” isn’t a term we chose

• The reality of living on PIP and UC

• GPs being told to send sick patients to the gym

• What real resistance looks like in a hostile system

🧠 If you’ve felt dehumanised, dismissed, or disbelieved — you’re not alone.
💬 Share your experience in the comments.
📢 And please like, subscribe, and share this episode to push back on the narrative.

👇 Resources and links:
🌐 Blog version: Wheeliemsadvocate.co.uk
📸 Follow me on Instagram: Wheeliemsadvocate
🧵 Join the conversation on X (Twitter): WheelieFUMS

#DisabilityRights #PIP #UniversalCredit #SickFluencers #WelfareReform #ChronicIllness #WheelchairUser #HateCrime #MSAwareness #DisabledVoices

The moment you’re diagnosed with MS is life-changing, and the emotional impact isn’t talked about enough.

I’ve written about what it feels like to process that news, and why taking time is not just okay, it’s essential.

💬 Blog post: MS Diagnosis Support: Why You Deserve Time to Process

Whether you’re ready to talk or still figuring things out, support after an MS diagnosis should always start with compassion.

🧠 Read more → Blog Post

#MSDiagnosisSupport #ProcessingMSDiagnosis #LivingWithMS #MSMentalHealth #ChronicIllnessSupport