Why do you think so many people associate mobility aids with weakness and incompetence?

Some people see mobility aids as a sign of weakness, that people have given up. Well these people are wrong. I know for me my mobility aids are in fact aids of freedom. Just look at what I have achieved this last year and continue to do. I have and I still am exploring places I never thought possible.

However, it may indicate dependence not independence.
Unfortunately because they haven’t been taught better.

I remember when I was against using an electric wheelchair in college, because it didn’t require me to use my upper body strength. I felt that the college was underestimating my strength. I thought it would make me lazy too. I absolutely love them now!

It’s been great to have the ability to do so much more now than my body would allow.
Unfortunately because it’s been the “norm,” and there hasn’t been a lot of awareness to prove otherwise. I always try to change people’s perspectives but there are still people who still don’t understand until it’s explained to them or they see it for themselves.

This is the one reason I would like to start posting more, but, social media is sometimes not used for the greater good, rather than people just wanting to be “influencers.”
It’s on because you could technically count glasses as a mobility aid.

Alternatively, aid and glasses are usually associated with competence or being smart. In other cases, it’s a sign of high intelligence.


Let’s flip the script and start telling able bodied peole that their legs (or other parts) must be such an obstacle for living a meaningful life.

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About Daniella-Jade Lowe

Hello, My name is Daniella Jade Lowe. I am a PURSUN researcher and I am working on marketing myself as an Accessibility Consultant. Journalism and Politics are my passion. I have a BA degree in History and Politics. What type of disability do you have? At birth, I was diagnosed with Spina Bifida and Hydrocephalus which are neurological conditions. As a result, I use a wheelchair for mobility. What is disability to you? The only disability is a bad attitude. I have a disability. It doesn’t completely define me; it just enhances me in a way which differentiates and strengthens me. My disability should be viewed as an ability: to see the world in a different way. I don’t really like the term because sometimes it indirectly implies someone is dysfunctional or helpless. The most important thing is to never make assumptions. Someone with a disability can be very, physically, fit and strong, highly intelligent and articulate. What has been your experience from the time you remember till now? - positive and negative experiences. My life as a wheelchair user has been generally okay. Wheelchair Accessibility is frustrating. I was teased a little in school. Other than that, life is great. How do you cope with: -daily activities - your disability, do you have times when you are down - people's reactions towards you. I have carers, a Social worker, District Nurses, a GP, and extended family in this country. I am also in contact with a local disability charity in Yorkshire. I also have a friendly landlord. How do you keep yourself motivated? I must stay organised and practice good time management. I also prioritise my plans. What is your word or advice - to those with disabilities? - to the society Don’t let people put you in a box. You have a voice, use it. 10. Tell us about your platforms if you have any- Blog: The View from Where I Sit Facebook: Daniella Jade Lowe Instagram: @daniellajadelowe/@theviewfromwheresitblog Thank you!