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<url><loc>https://samedifference1.com/2026/04/13/dancing-is-about-what-you-are-and-what-you-can-do/</loc><news:news><news:publication><news:name>Same Difference</news:name><news:language>en</news:language></news:publication><news:publication_date>2026-04-13T00:20:40+00:00</news:publication_date><news:title>&#8216;Dancing Is About What You Are And What You Can Do&#8217;</news:title></news:news></url><url><loc>https://samedifference1.com/2026/04/13/first-student-win-of-the-year-i-passed-my-level-three-end-of-life-and-palliative-care-diploma-here-i-am-proudly-showing-off-my-diploma-certificate-i-worked-so-hard-for-them-because-were-d/</loc><news:news><news:publication><news:name>Same Difference</news:name><news:language>en</news:language></news:publication><news:publication_date>2026-04-13T00:00:00+00:00</news:publication_date><news:title>First student win of the year. I passed my level three end of life and palliative care diploma, here I am proudly showing off my diploma certificate. I worked so hard for them, because we’re disabled it doesn’t mean we can’t achieve. Opinions of funding bodies and local authorities need to change because we can achieve! We   need support from them that cost money that they can’t be bothered to invest in us.</news:title></news:news></url><url><loc>https://samedifference1.com/2026/04/12/i-am-not-just-disabled-i-am-a-wheelchair-dancer-who-takes-part-in-inclusive-dance-projects-here-is-what-they-dont-realise-the-right-support-can-open-up-a-persons-world-here-is-m/</loc><news:news><news:publication><news:name>Same Difference</news:name><news:language>en</news:language></news:publication><news:publication_date>2026-04-12T01:00:00+00:00</news:publication_date><news:title>I am not just disabled. I am a Wheelchair dancer, who takes part in inclusive dance projects. Here is what they don’t realise: the right support can open up a person’s world. Here is me participating a few Sundays ago, when the right support and funding was made available. Even though they only made it available for five weeks while am ill. The reality is: they think that my needs will go away after 5 weeks when they certainly will not. Every time I get a flare up or my condition worsens, I need at least 3 months for rehabilitation, as a bare minimum. This is also for figuring out what my new support needs are for me to still have a life which I am happy within. Just because they and I hope it will go away in five weeks, I know realistically it will not. FND can be invisible until it’s very visible and the person like me is in crisis.</news:title></news:news></url></urlset>