Come and join me for some juicy questions, and a cook along. Videos mentioned: Last video: kzfaq.info/get/bejne/hJejerR405qsn5c.html Confidence in a wheelchair: kzfaq.info/get/bejne/i992i6uVzpyuqIU.html Staying positive with a disbaility kzfaq.info/get/bejne/i992i6uVzpyuqIU.html Work dramas with Jessica OOTC: kzfaq.info/get/bejne/iMp2ia6gl9rDo5c.html

I am in chronic pain and my life is controlled by it, so I would take a cure in a second. Not because of the chair, only because of the pain.

I find that in terms of being cured it's like...I want a cure for my chronic illness symptoms, ie, I would like to be able to work my dream job, I would like to do the exercise I used to enjoy, I'd like to not be in pain all the time etc...but people assume I want a cure so I can walk again. Like, no, walking is the least of my worries. I don't want to be cured so I can walk, I'd like to be cured so I can do things I enjoy and not suffer for it.

an ablism video would be great. recently when my mum mentioned to a family friend that we (I) were looking at wheelchairs for me to use they asked "why does she want one of those" and i was so glad i wasnt around so mum dealt with it

I’m a total yes for pineapple on pizza and armburgers. As someone who is disabled due to chronic illness, I do wish there was a cure. For me, but also for the millions of people who live with post viral conditions, like ME/CFS and Long COVID.

I think some people with higher up disabilities like mine at C1 would love a cure or to just rewind time ☹️

Being in my wheelchair I feel like I live in a world of giants even though I am 6 feet one inch. But, I am use to this now...

Yes! A “cure” would mean losing my identity as a disabled person and all of the beautiful things that have come into my life as a result. People occasionally put their hands on me and pray for me in public, normally without asking, and I’m always just like, “Whoa whoa whoa! I don’t want to WALK, take that back!!” 😅

Everybody exists on a spectrum of "ability", the average person doesnt have the same abilities as an olympic sprinter, yet we dont think, oh how tragic you must wish everyday that your body is different. As a disabled person I think things were accessible to me rather than for me to be different

Years ago I used to work for a major supermarket chain. Back then I was still able to walk with crutches. But I couldn't manage stairs, and our store was on the first floor. Someone accidentally set fire to the toaster in the staff room, so we had to evacuate the shop until the fire brigade came. Guess who had to wait at the top of the escalator? But the upside is, I got carried down the stairs by two firemen.

I don’t want a cure either. The only things I remember about walking are with clunky braces and a walker. Also the surgeries and recovery are terrible. I’m in no pain and happy how I am!

I once was involved with a fire drill in a hotel. The problem was i was there to take part in the national junior athletics championships for disabled people, so there were literally hundreds of us in all the hotels, and the fire department had insisted all hotels do a drill this weekend. It was carnage. PEEPs werent a thing back then, it was everyone for themselves.

Evacuation story: Downtown Washington, DC on 9/11/01. My wife and I worked in the same building; she’s the wheelchair user (power). Absolute chaos; the only evacuation plan involved vacating the building in case of fire, not evacuating the city. I made it down to our van in the parking garage fairly quickly, but I couldn’t get hold of her to tell her where I was for at least an hour because the cellular circuits were either overloaded or jammed citywide by the military. I finally drove out of the garage and picked her up in the street. Then we sat in absolute gridlock in front of the Capitol building while Flight 93 was still airborne. We finally found our way out of the city and home after more hours than I care to count. Did I mention that it was our daughter’s first week of kindergarten, and my wife was 4 months pregnant with our son? Yeah…

I also plan how to get out if there was an emergency. As a wheelchair user I think it's important to have a plan. Years ago I worked in a multistory building on an upper floor and my friends were concerned about how I would get out in case of a fire. They came up with a plan and met with all these strong able-bodied guys. Then they drew a stick figure of a woman in a wheelchair with flames and then put the universal symbol for "no" (circle with diagonal line through it) and these were placed in every volunteers cube so no matter where I was would know who was willing to carry me out of the building. They called themselves the "Don't Let Barbara Burn Committee". It was so thoughtful and kind. They wanted me to teach them all the best way to carry me, etc. They were truly wonderful guys.

A video about ableism would be great! My whole life people told me I need to push thru, need to keep going and go thru my own boundaries. That placed me in a wheelchair and people still tell me oh do you really need it, it will get worse etc, bwaaaa My disability is a difficult one, because it’s not as ‘clear’ as for example an accident which causes the disability. And people just don’t understand. I didn’t know the word ableism but since I learned the word, a lot fell in place. So yes please, I would love a video about it!

I needed my disability to be where I am in life now, but would I take waking up able-bodied tomorrow morning? Abso-blooming-lutely! Life would instantly be many, many times easier.

Four years ago both of my hips were shot. I had to use a cane. That opened my eyes to how difficult it can be being disabled. Even crossing the street I was always afraid of getting hit because not everyone is patient. And there was at least one close call. I’ve never forgotten that experience & am more aware now. Especially since not every place is accessible even if it’s a newer building.

6:02 yep same thing happened to me. I got invited to a friends Hen's night. Her mum called the place to double check there was wheelchair access and she was told "We only have 1 step, but she will not be allowed in as she will be an insurance risk".

Gammon egg and pineapple is a British pub staple, in Germany we have Toast Hawaii, which is ham, pineapple with grilled cheese on, yes, toast. I have seen far worse pizza toppings. For me, tuna on pizza is a big no-no! Another great video. Freddo the wheelchair guy on YT, on his Apes on Tape podcast discussed the question, too, would I want to be healed.

Iv been discriminated against due to my epilepsy. From as a kid being told I couldn’t join girl guiding, to as a teen not being allowed to go on school trips to France, to after college places not giving me a job because of my epilepsy, to managers in voluntary jobs taking advent of me due to my epilepsy & autism. 10 years after leaving education of some sort and I still don’t have a permanent full time job. It’s so frustrating at times. So I fully understand ableism.

I went to the theatre with my mum a few months ago. The show had been postponed for a couple of years due to the pandemic and at the time we bought the tickets my mum had some health and mobility issues, but nothing that most people would notice. However, by the time we actually got to go to the show she was using a stick to walk a lot of the time and struggling with lots of steps (which shouldn't be relevant, but will be later). Our seats were in the front row of the upper circle, so once we were upstairs it was fairly level. The theatre had a functioning lift and accessible toilets on every floor so we didn't have any issues beyond needing to move for people who needed to get in and out of the row (especially the impatient ones!). At the end of the show, we decided to let everyone else go first to make it easier for mum to get out of the theatre. However, after about half of the audience had left the auditorium there was an announcement that everyone needed to evacuate the theatre immediately with no real explanation. So we gathered our things and started to make our way out. Then an usher appeared and tried to hurry us out, even after mum had explained that she couldn't move quickly. There were about 3 steps up to the doors, so mum was taking her time (hampered by the fact the usher had put her fluorescent jacket on the handrail). This continued as we got to the top of the stairs with more and more staff members flapping about how to get mum down the stairs, with no clue what to do (there were still lots of people on the stairs at this point so no rush really). Eventually someone piped up that they had an evac chair, but by this point mum didn't feel confident in their ability to use it safely so declined. Once the stairs had cleared a little, I started to help mum down the stairs with the people in hi-vis still flapping around us. Each floor we got to we collected more and more concerned hi-vis people, who to be frank made the situation more dangerous. The first incident was someone who, whilst I was trying to concentrate on helping mum, asked me where we were sitting and replied with "maybe you should think about that next time". I was genuinely lost for words. Apart from the fact that mum could walk perfectly fine when we booked the tickets, it wasn't our fault that they had no real evacuation plan for disabled customers. The next unhelpful person was someone who as soon as a hint of smoke started to appear kept repeating a mantra of "This is serious, we need to hurry!", as if we were purposely taking our time. Then, there was the member of our hi-vis escort who thought they'd be "helpful" by grabbing mum's arm and nearly toppling her down the stairs. To top things off, the second mum's foot touched the ground floor they all scarpered and only the security guard stayed to make sure we got out safely. By the time we got outside, there was no-one in sight whatsoever! Luckily there were some decorative rocks outside that mum could sit on to recover. The whole evacuation was like a health and safety video where people have to spot all the mistakes, they wouldn't even let us use the emergency exit so everyone had to use one staircase! So, if you have a disability (or even might break your foot just before a show and need crutches) then avoid Aylesbury Theatre. We think the emergency may have been water from the show getting into the electrics, but it obviously wasn't major as there weren't any emergency services around. Even when we went in the pub over the road to use their loo (the pub was very accessible by the way, they even had a wheelchair ramp inside) nobody like the fire brigade had turned up.

If I could, I would take cure for my disability. The sweet, sweet vision of not feeling pain everyday.. I have double scoliosis, ostheophytes, uneven amount of ribs, discs protrusion, chronic migraines, bipolar disorder (and recently hallucinations, yay) and GAD. So a mix of every disorder that my family had. But I understand the fact that you think you could lose your identity. I also don't know any other life. Maybe life on heavy painkillers, but my psychiatrist doesn't allow me to take them anymore, since it messes up with my other meds. About the most controversial one, before I was vegetarian I loved pineapple on pizza, but now I don't see a point 😂

Really enjoyed this video. Thank you for answering my question. I have never heard of abelism before. It would be great to have a video on it please

well i know watching your videos has help me, from stupid and painful comments from strangers, doen how to wheelie ,and getting Shaun to have ago lol which he did well, so keep them comming and thank you

I do like this style of filming as it's cool to see the way you move around and do things as someone who's just about to get my first wheelchair but some of the noises make it difficult to hear and process what you're saying, stuff like the spinach bag rustling, some of the frying and stirring noises. So it's good but better with quieter background noise. I'm slowly working my through your videos and they're helping me feel a lot better about being a new wheelchair user so thank you for that! There's so many little things I'd never thought about before that it's been good to learn about.

That food looks yummy!! I don’t think nondisabled people understand that for some of us disabled people, suddenly becoming able bodied would be like suddenly becoming disabled, but in reverse. I have been disabled my whole life so suddenly being nondisabled would throw me into a world I know nothing about. I don’t know how to function that way!

I feel so accepted and seen on your yt channel! Always watch your videos when I’m struggling 🥰

It took me SO long to get to the point where I proudly identify as disabled, despite being disabled from birth. I think this was the best thing about the past 2 years and lockdown for me as I had the space to finally just sit with myself and meet other disabled online who gave me a sense of community.

Personally I appreciate your videos when I was getting my first wheelchair I looked at your videos for advice. Now I’m a part time wheelchair user so my experience is different but it really helped. I would like to know your experience with uneven surfaces? I use a powered wheelchair and I tighten my muscles in my core and my legs a lot with uneven surfaces, and I thought I would ask how you handle these situations

YES, Gem! Pineapple on pizza is definitely for the win! I loved watching you cook and I’m still obsessed with your kitchen 😂

i really like this style for more informal and Q&A videos. would you be open to doing a wheelchair newbies guide? tips and tricks you wish you knew earlier? or a guide for beginners? im getting my first wheelchair in (hopefully arrives) October, whilst i have a power add-on (efix) for my less able days im hoping to keep and build muscle from using it manually.

I would take a cure in a heart beat. I hate not being able to do things for myself. Perhaps I would feel differently if I was in a more suitable property with better access and proper adaptions for my various issues instead of reliant on a stranger coming in every day to do things for me. I hate that. The pain sucks too, and paying a small fortune for a car I barely use because I can't get out to it easily but couldn't do anything at all outside without it. I don't see being disabled (or autistic) as part of my identity and I have no interest in activism, I just want to be independent again. I never needed anything from anyone and now I can't do anything. It's miserable. I'm sure if I had been disabled from childhood I would feel differently, but I was able bodied until 30 so it's been very difficult to accept, and there is so little help out there for disabled people.

Oh no Gem say it isn't true please Gem LOL Good news A fireman bagged an payed for my groceries last week so wheels aren't always a negative Love 😍 from TEXAS

Hi Gem i just so absolutely love all of your beautiful videos so very very much you are such the most sweetest beautiful gorgeous woman ever in the whole wide world i love you Gem.

I always check where (emergency) exits are and have an emergency plan and bag. This stems from my time as a firefighter though so not disability related. Just heard "I didn't think it would happen to me/us" waaay to often. I picked up the bass again in January this year after 7 years of not playing after my SCI, it helped improve my hand function massively. You'd be surprised what you still know and how quick some things come back once you start playing again. Other things have to be re-learned though. Pineapple on a pizza? I'd rather not suffocate thank you. I have latex allergy so it would literally kill me.

I made a video about would I want to be cured of my SCI a few weeks back, what a coincidence. It came from a dream I had where I wasn’t in a wheelchair and kinda missed it. Either way, it’s complicated, I don’t mind my disability but I am also coming from a privileged position of a low level paraplegic, no nerve pain etc. Would I take some healing? A solid maybe

I love this video thank you so much! And that pineapple pizza sounds good I don't know about the burger LOL thanks for posting! God bless!

The hardest thing for me to deal with is other people especially professionals like OTs. Since using a powerchair and a hoist I feel like I’m in the “written off” category and worthy of no help. Physios washed their hands of me many years ago xx

Chronic foot problems for me, and I frequently am on crutches. More often than not I won't go out of the house on my crutches, despite the pain, because of embarrassment. I don't want to be seen on crutches! However, my late wife would say, "If you are having a bad foot day and feel that you need to use your crutches, go for it. Only YOU know your body . . .and to hell with what every one else thinks." Any comments, folks? How do my fellow subscribers believe?

Gem, I absolutely love your new kitchen! Great colour scheme as well!

I’m so glad you make your videos Jen, I came across your channel recently and I’m really been enjoying them

I'd also love a video on ableism, especially if it also mentioned ableism from inside the community. I've dealt with ableism from abled and disabled people but people rarely mention ableism from disabled people which imo, causes a lot of damage.

Thumbs up on successfully multitasking! 👍🏼

Pineapple on Pizza and Burgers???? You belong Down Under my friend!! Thanks for all your help and insight, I just got approved for my wheels yesterday and I am looking forward to Rocking them out when they eventually arrive!!! Yay!! Miracle cure? I would take away the pain YES! Cure to be out of the chair....sometimes when things are difficult to access but on the whole I have no problem being IN the chair, just the idiots who ask to be run over when I go shopping 🤣

I don't eat grains or their products, fruits or dairy because I am low carb because of diabetes. But, your cooking looks good. Thank you for helping others....

I realise it is speeded up, but I love the way you just whizz around the kitchen in your wheelchair,

I was born with spina bifida at 15 I lost my left eye. I wouldn't change a thing. the only thing I would change is in the last few months I have gotten to where it is too painful to walk even with a walking aid. I now find myself in the last week in a wheelchair. Not sure if I would change that. I will admit being in a chair right now is the hardest thing I have ever done so many things I never thought about, on how hard it would be to get around. I am not sad about being in a wheelchair to me it is a new adventure in life. I can't change it so why cry about it. I do have my bad days. But I have followed this rule in my life “Improvise, adapt, overcome”

Growing up I was always ask by other children and teens if I would have a cure for my autism. I would always say no as it is part of who I am. As I have grown older I have developed/ diagnosed more disabilities some that make my life harder ( fibromyalgia and cronic fatigue) as they make it hard to mange my other disabilities. The only thing I would what to change is having more energy and less pain.

I’m often not on board with a sweet/salty combination. I think it works well with desserts and some Asian food, but I don’t get down with putting pineapple together with tomato and cheese. So that would be a no for me. 🍕

Hawaiian pizza and banzai burgers?? Count me in!!

I thought I was the only weird one I always make sure where the exits are and the toilets I don’t know why but I still do lol I’m weird I know. You are so positive and enjoyed this video a lot and thank you so much for sharing this video. I love your videos and you make the videos you want to do I’ll enjoy anything you bring us so this was great and I love pineapple on a pizza and yes being Australian I put bacon and sometimes pineapple on a burger lol so good

Thanks Gem, another awesome video.

That rice looks so yummy. It reminds me of the chicken bowl from Chipotle. I don't know if where you live you have Chipotle restaurants but its very popular in the US where I'm from.

😂😂😂 Pineapple on Pizza my son in law turns green my face lights up. As for Pineapple on Burger I love it. I hate Buger Buns so use lettuce and Pineapple to top and bottom of Burger instead awesomeness. Getting your head round using wheelchair is not losing independence but gaining it is hard to get your head round but once you have life starts in a new way. I use that saying about no one cares what your doing, wearing, look like they are way to busy worrying about themselves and what folk think or attached to phone. The 1 thing I would want more of is well maintained dropped kerbs with double yellow lines so offence to park on them. My confidence has been shattered when poorly maintained kerb crumbled in winter and I fell in wheelchair attache8by seat belt face down with power chair still attached into road did cars stop nope however a group of young teenagers boys and girls ran over stood in road stopped traffic, helped me up and made sure I was OK and offered md a coffee with them.... Needless to say they got a huge TQ and a little something to treat themselves

To much in this video to comment on. But having been disabled at the age 50, I know what it was like to not be disabled. So yes, I would be ecstatic to be rid of my paraplegia and back to what I was like before my accident. I truly think you would also be ecstatic once you found the possibilities without your disability.

Great video! Also love the Minnie shirt!

Great video!

That looks amazing!!

I have learned more about being a good human being from my disability than from anything else in my life. I wouldn't trade it either, as hard as it has been and continues to be.

I’m amazed at how often I say,”Excuse me.”GO figure.

When can we come round for dinner!? Very enjoyable video, great work

love your videos 🙂

I'd love a cure. Yeah, disability has become a big part of my life and I have pride in my disabled identity but I'm suffering and lost my life. I had plans, ideas, etc. That are no longer possible due to illness. Not only that, disability is expensive. Meds, mobility aids, etc. I'm proud of being disabled but I'm suffering and if I had a choice, I'd choose not to suffer.

Thanks for posting this. Nice to listen while I did the boring washing up. Now with a clean kitchen...what do I eat? :) Not pineapple on pizza.

Well, I'm not there for pineapple on a pizza, but, then again, I don't like pineapple. Pineapple, except with a pineapple upside down cake, is a no, and even then, I wouldn't want too much pineapple there...

I just found out I have ehlers danlos sydrom and I'm getting a wheelchair but right now I have a temp chair. If there was something I would take to lessen the symptoms I would take it I'm in a lot of pain today. I also love pineapple on pizza.

You are you, disabilities make us unique and different, i'd rather have that than been bland. As for 🍍on 🍔 and 🍕 equals 🤮.

I am also a sci patient you are doing 😃 great work

I have a question but do not want to be obtrusive so please do not answer if it is. I was wondering if people assume you can not be sexually active or fulfilled because your in a wheelchair?How do some people react say if you went to buy lingerie or sexy dress. I know the answer but feel it's a important question so many non informed people could be informed better! I loved both vlogs as you cooked and talked. Your a beautiful woman and I love your dedication to your channel. The love Daisy shows you thru her service and dedication to helping her mum. She is a one in a billion, you are so very blessed. I hope this is not too obtrusive but sometimes it takes hard questions to educate others.

I like how your kitchen is set up so you are able to get so close to the hob while facing it straight on! I really do enjoy your videos, they really do shine a light of hope. I would love to see a video on ableism and possibly polite yet clear ways of standing up for our rights. Sometimes I just don't have the energy/capacity to fight for myself. Like when I am in so much pain and struggling to just breathe, I must choose breathing instead if literally wasting my breath explaining myself to someone. Now about adding pineapple to a burger, if I could grill the pineapple, I think it would be reasonable to give it a try on my black bean burger.

I've been a paraplegic for 43 yrs, with atrophy and none density, it would be so extremely painful to gain feeling now. Also I wouldn't be able to use my legs to stand

I might gonna steal your idea with the pineapple on the burger, sound interesting:)

Some juicy questions...unlike those pineapples put on pizza😂😂😂

👏🏻💯

Of course! But I'd also accept one extra arm or a special 10-minutes of standing per month to get some hard to reach chores done. ;)

Not allowed into a club. That’s discrimination. Fire hazard my 🤬. A fire hazard is something that causes fires. I get they think you couldn’t get you out safely but then they should say that not call you a fire hazard. Id be fuming if I’d been in your place.

Interesting mention of ableism. I've dealt with HEDS for about 46 years in terms of musculoskeletal issues, but realised it started earlier with other things like migraine. I knew I would be discriminated against if I let on I had health issues so did my best to hide them. Most people did not realise I was ill. Now with braces and canes etc it is more obvious and my invisible issues are more visible and I've experienced open hostile ableism in a few forms and now ageism as well from some ignorant b..ds. I also endured sexism in some employment situations as have a lot of women. But only heard about ableism from your videos. But now I've decided on a strategy of "calling out" bad behaviour, then walking away and avoidance. Weirdly, it has mostly occurred when I'm simply grocery shopping. Go figure. Or getting onto buses during Covid and not being able to use the "accessible door", but they let people with prams use it!!

Please do an ableism video. I remember one incident when a woman asked me why do I even bother going out if I'm suffering with an illness. Smh.

Okay, Gem, I’m not going to unsubscribe, but pineapple has a place and it’s not on pizza lol! What a wonderful world we have to be able to make choices for ourselves! Viva la différence!

Nope. Definitely no pineapple on pizza 🤮 However pineapple in a burger with lots of chilli? I'd try that 👍

I would take a cure for SCI in a minute. I know not everyone would choose cure for their disability though.

My thought on the staring thing ... speaking from a guilty person ... I catch myself these days. Anyway ... the thing is that my thought are (and likely most if not all others) is things like.... I wonder what happened?, I bet it was painful, I bet it is painful, I bet it is hard, How do they [insert many things here], those types of things. But think about it ... those are the thoughts that give rise to empathy. Shrug ... don't know if that helps anyone .... just my two cents. I would also note that because of back troubles I am now considered disabled ... so now I'm on the other side of that equation.

I also enjoy pineapple on pizza. And as to a cure, yes, I do want one to be found, but I'm unsure of whether or not I would take it myself. There's so much that I've experienced and learned through having EDS, and I wouldn't trade that for any cure. But there are definitely days when I wish for the pain to go away.

You didn't know that ableism was a thing until 3-4 years ago? I need to move to your country. I was born deaf but learned very quickly about ableism as a very small child. I was bullied and mocked for my voice (I was forced to learn how to speak instead of learning ASL), adults would chastise me, teachers would constantly berate me and tell me to pay attention (I was. I couldn't hear them), then they would call me a liar for saying I was, I was always gaslighted, etc. I grew up thinking I was stupid and believing I would never amount to anything in my life because I was worthless because of my disability (Had a teacher legit tell me this to my face. Then lied when my mom confronted her about it.). It took me years after graduating high school (which was something people always told me I would never be able to do) to finally get self-esteem and learn my worth and overcome so many things. So far now in life, I have done almost everything people told me I would never be able to do. My next goal is graduating from college. Yes, I have people tell me to drop out because it's too hard for me and I won't be able to get a job anyways because of my disability. I have two classes left and I am about to graduate very soon. Thank you for saying that your disability is who you are and is your identity. My sister who is nondisabled does not understand. She doesn't believe I'm deaf. She says I'm making my hearing loss worse than it is, does not believe and thinks I shouldn't use my deafness as my identity, does not believe I can be culturally deaf, and says I need to stop attacking the family (when I told her it would mean the world to me if my family would learn ASL to communicate with me), and also says I need to stop getting offensive (whenever I get frustrated with the constant ableism I deal with every day). I've never really had the best relationship with her, but we used to have a sisterly bond. When she got pregnant with her first kid, it was like a switch went off and I barely know who she is anymore. She's more aggressive and dominating. I have just learned to back off, especially upon discovering that she denies what literally makes me, me. Pineapple on pizza. If you like it, do it. I used to get made of for putting mushrooms on pizza, so I stopped doing it until I was an adult. It is fun watching you cook or whatnot while doing your video, but can I make a suggestion? Can you not bounce the screen constantly back and forth? It is distracting and hurts my eyes and gives me a headache. If you need to switch between cameras, can you stay there for at least 10 seconds before switching back? Especially when you're not even looking at the camera behind you.

I hate sweet and savoiry combos, but like people can do what they want with their pizzas. Just put my pineapple in a bowl and that will be my dessert ^^

I love playing so how do you use the petals? Because before I was playing. I was teaching myself piano but now that I have more troubles I can't really use the pedals when I'm playing piano. So I'm just wondering how do you deal with that and make adaptions?

How do you get this chair.. I'm from Egypt ❤️

What about an awesome exoskeleton ala 40k Mechanicus?

Ill HAVE to try a burger with a pineapple ring on it!!!

..it is just a word for subdivision of discrimination or prejudice.. honestly, i don't waste time on that..sun-glasses is my own solution.. I'm in my 40's, and life is short, so the time invested on those people or thoughts, is zero from myself! .. There are billions of people..even if, the good/bad people ratio would be 50/0, my time would not be enough to meet all of good people.. i make a triage the earlier i can, to invest my time on good ones! About future of channel,..just follow positivity! .. ..maybe give a try on just reacting a movie or funny memes or so, time to time..diversify.. just an idea for your sea of opportunities of fun stuff you may like..

I made a comment about Bones but A Million Little Things also has a wheelchair user story line I’d love to see you’re reaction to. ⚠️⚠️⚠️Sppilers⚠️⚠️⚠️ Eddy gets in an accident and becomes paralyzed. I’m currently in the middle of watching this story line, but I’d love to see your reaction. I feel like it pretty accurate but I’m not a full time wheelchair user. I could provide time stamps and episodes for this too!

YES! Team pineapple ALL the way! 🙌

Yummy. In my answer to people as to whether I want a healing I scream, I AM NOT YOUR SPIRITUAL PROJECT TO ALLOW YOU DIRECT ACCESS TO HEAVENLY DIVINITY. I use my chair I am having one of most days and I am very thankful for my wheels and THE LAST THING I NEED IS FOR SOMEONE TO ASK ME TO FEEL BAD. I also use a cane or walker at times the same applies. I once told a person if GOD wanted me “complete” then he would grow back my finger, and fix other structural stuff to which the person replied, “nah he won’t do all that you crazy.” 😂 Sometimes being a normal me is fun as I was diagnosed in my early twenties with spinal deformities and did some pretty amazing stuff.

Oh No I don't know if I can continue to watch you now. How dare you put PINEAPPLE on a pizza... LOL It's all good.

I love pineapple 🍍 on pizza. Hawaiian pizza is my FAVOURITE & my go to pizza.

This is a dealbreaker I got to unsubscribe because of the last answer like how dare you! Nahh just kidding love your videos 🥰

I'm not sure if I have a place in this discussion due to my disabilities being invisible, autism, dyslexia and dysgraphia. One thing I would say is I'm surprised pineapple on burgers is controversial, I thought that was how you made Hawaiian burger.

I will keep watching in spite of your pineapple on pizza. :-)

I love pineapple on pizza and I've had it on burgers too.

What about how to identify ableism? 'Cause not all ableism is so easy to identify.