I Am Invisible No More: Part 1


My name is Effie Koliopoulos, I live with an
invisible disability and illness. I was diagnosed with juvenile arthritis and
autoimmune disease 15 years ago. While arthritis is the number one cause of
disability in the United States, there are still people living with this condition who show
no signs of being sick or disabled. That is because invisible disabilities and illnesses
are not black and white. There is a lot of gray matter that
isn’t understood well by society. I’m one of those people that doesn’t use a wheelchair or any assistive device in
fact growing up I was a healthy active kid until I started experiencing strange
symptoms that didn’t go away when I told my doctor at the time about the fatigue
night sweats random joint and muscle aches I was told it was just growing
pains of being a teenager and nothing to worry about
that I would outgrow it but I didn’t and many people out there with stories like
mine didn’t either instead we grow into it and have to come
to terms with our new life many people suffer in silence for years because they
are not taken seriously then we start doing research on Google or other
sources to try finding answers in order to be heard and validated society and
mass media doesn’t make this inner turmoil any easier if someone doesn’t
fit the mold of what a sick and disabled person is supposed to look or act like
they are questioned and harassed I had this happen to me 10 years ago when a
stranger called the cops a complained that I was misusing my disabled parking
placard at the train station sometimes the people closest to us don’t
even understand what we are going through illness doesn’t just affect one
person it impacts everyone around them from their family children friends
co-workers and loved ones or some their number-one supporters are those closest
to them assumptions create a barrier between people who are living with any
illness or disability in the outside world
because of this feelings of grief depression anxiety fear and social
isolation can start occurring there is more to illness than pain and
inability to walk there can be medical debt side-effects
or medications constant doctor appointments being told to prove your
illness or disability the unpredictability of feeling good one
moment to horrible the next mental and emotional pain strain relationships not
being able to work full-time or at all and having your faith tested the stigma behind you are too young to
be sick is what drives us lack of awareness invisible disability and
illness doesn’t discriminate anyone at any age can find themselves in this
situation nobody should have to live in fear of being approached in public
called fake a liar or reporter fraud excuse me that placard isn’t mine 9 out
of 10 people would challenge someone who doesn’t look disabled because they think
they are doing the right thing that disabled man really needs a spot it’s
people like you who fake it who are causing problems people don’t need to wear signs that
illustrate what they are going through in order to be treated with kindness but
what if we could read what was going on in the lives of those around us what are
we still care to question them or do we stop and think before reacting
either way the reality is everyone is going through something whether we see
it or not thank you for watching please help raise
awareness for invisible disabilities and Commerce’s by sharing these videos I
want to thank lusco video all my Kickstarter backers who helped make this
video come to life and especially global healthy living foundation crystal bought
a fur ester a balton Kimmie and rheumatism anak along with everyone else
who took the time to share their photo and opinions in a video be sure to watch
more of the I’m invisible no more videos subscribe to the channel and make sure
to give our videos a thumbs up you you

14 Replies to “I Am Invisible No More: Part 1”

  1. Wow! Excellent video! Thank you for being a part of our #IAmInvisibleNoMore Campaign! We are going to add your video to our playlists and share on social media for #InvisibleDisabilitiesWeek! Thank you for bringing awareness, education and support for millions living with illness, pain, injury and disability!

  2. We (Lisa and Becky) at #CentralPainNerveCenter give you 2 thumbs way up! This is EXACTLY what our invisible disability community needs! GREAT WORK EFFIE! Can't wait to see parts 2 & 3. #InvisibleDisabilitiesWeek #IAmInvisibleNoMore #CentralPainSyndrome

  3. Excellent Job! So many people struggle every day of their lives with an invisible disability. Kudus for bringing awareness to society for helping to break the stigmatism. #IAmInvisibleNoMore

  4. From MK and I thank you for sharing. The kiddo has several issues from birth, the main one being CVS = cyclic vomiting syndrome. And I have arachnoiditis plus so many more…

  5. Thanks for putting this out there so people that may not understand what invisible illnesses are all about. I have a plaquard and on my good days I feel guilty and park in a regular spot but try to stay as close as I can. On my bad days, never fails, I can’t find a handicap space at a particular store! I’m also in denial over using the scooter. I struggle with my cane at the grocery store but am so afraid I’ll knock over displays!

  6. Effie – so well done – we cannot wait to share this video with all of our 'knee people'… 🙂 Your Friends at X10 Therapy

  7. I loved this. I have severe defense osteoarthrtis if hip osteoporosis compression fracture and now lymphoma. I'm still trying to work though times I can barely walk. Abd get this my g p will not give me a handicap placard. I've asked 3 times I feel so unheard. Thank you for speaking up for marginalized people.

  8. Wow – thank you so much for putting this together. Invisible disabilities are so often so unnoticed yet people are so judged. I will definitely be sharing your great work on increasing awareness around Invisible disabilities – thank you!!

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