Відео

….i can easily tell that you have type 2 diabetes

Have you thought about doing a video about Kaya? She’s frequently posted on the subreddit. She has a documented history with ED which led to a series of corresponding problems. Yes, she posts a lot. Yes, some of it could be considered attention-seeking but I really see it as someone excited to share their journey. It’s just hating her for existing at this point. Any criticism of her could be construed either way, and that’s what’s inherently frustrating about subreddits like these. If they are faking, and have factitious disorder, they have mental illness and are being unfairly targeted. Why exploit people who are already clearly suffering?? It’s especially cruel.

Im happy your back i hope your feeling better

Jacquie wasn't a fake why are people talking shit about her

Amber Lynn isn’t bullied because she’s fat (not by the majority) she’s criticized because she’s a liar and has done awful things to people in the past.

Dani is truly sick. Just so sick. She desperately needs psychiatric hospitalization

Also would enjoy a vid on your take on ALR and maybe on the community that follows her? I personally have my qualms with her but also with some of the folks that make content about her cause it feels hypocritical but there’s some valid stuff too!

Unrelated but I wish you success and happiness and peace at your new job! May the interim hotel stay be a good one 😊

Just now seeing this video. Laying down in bed in pain. Seizure yesterday toilet tonight ibsd sucks on the verge of emergency room visit let them stick my port. I need advice anyone wanna take a Crack at it kind of reminds me of a girl ex friend who i am trying to get rid of

Thank you so much for making these videos it's greatly appreciated

Thing is we all know our bodies better than Dr's do but it's still best to seek medical advice before self diagnosis because you always need a good option for your personal health and well-being or chronic conditions. I have been diagnosed with gastropreasis and a lot of multiple conditions which is why it's called chronic illness. I have general ptsd and anxiety. But I feel that it's best to get it on paper form for better ways to care for your own health and wellness

That is frightening. An ENTIRE sub-reddit dedicated to a random Ci patient? CREEPY! Also you look very nice - the colors/hair are really working for you. Good luck with your new job and move.

Dani M and Ash C. now have their own sub Reddits.

I vaguely remember people saying she was eating stuff like fried chicken instead of following a diet for gastroparesis where she wouldn’t need to resort to a tube. Basically it seemed like she was somewhat noncompliant and causing at least some of her GI symptoms with a poor diet. Good videos btw, interesting topic that hasnt been covered much.

Thanks for helping spread the word about the illness fakers community because for those of us with real chronic illness like myself I have gastropraesis and hypoglycemia and I was born with cerebral palsy. I also have POTs its all diagnosis later in life for me as well but I have had symptoms since I hit my teen years its just the technology was not that good back then. But thanks so much for helping the community.

Um... medical stuff grosses me out (like have spoken with a therapist about how much). Also I'm not autistic. I would argue that using terms like "abdominal" vs "stomach" can simply be an indicator of an intelligent and nerdy person. Those words technically mean two different things...

I feel she needed mental health help as much as anything.

I’m confused as she seemed to be so fake.

I’m in the group I love your summary Do Dani!

Thanks for the update. I'm sorry that the diagnosis wasn't what you hoped for and hope that your doctors can find a treatment plan that will help with the insulin resistance. Wishing you all the best!

great video! i'm sure jaquie would love to see people defending her like this. in the future, do you think you would consider making videos in defense of other disabled creators who have been targeted by groups like illnessfakers and kiwi farms? they need someone on their side too.

I'm so glad to hear you're getting the care you need, especially with diabetes. Having to force yourself to eat when blood sugars are dropping is the pits, especially when you're sick. As for the pump, I wish you all the best. I don't want to say that I hope you get reclassified as Type 1, but I think it might be helpful for management.

That was a great video explaining how a handful of medical conditions can cause even more medical conditions. Each of the "symptom" conditions still has to be dealt with on its own and so the reality is that you are treating twenty issues, even if you have only five parent conditions. It can be frustrating and overwhelming for the person and for those in their circle of friends and caregivers, it can be really confusing because they don't know how to help.

I'm always fascinated by Illness Fakers content. I knew someone who had Munchausens, we were very close friends since we were kids. She was always prone to exaggerating minor injuries and colds and stuff, but when I was diagnosed with my chronic illness, it was like her Munchausens went full blown. I eventually had to distance myself because I realized that spending time with people who are actually ill seemed to be a trigger for her, like it made it worse. I realize that it's a mental illness so I try not to be too harsh about it.

I knew her in real life. Met her when Harlow was 3/4 months old. Trained with her and was friends for a bit. When I met her she said she had narcolepsy. Thazzit. Hung out with Janice and Orion too. Janice also said narcolepsy and potentially going deaf..we fell out shortly before she got the feeding tube and before the wheelchairs showed up..she’s better than Janice BY FAR but still they’re not great people overall and I’ll leave it at that.

Great advice, especially on the emails. Recording everything in writing is essential. Even if they verbally agree to accommodate you, sending an email thanking them for the accommodations that they agreed to (including a list of those accommodations) and saying that you look forward to their classes is another way of confirming their agreement in writing. Although it can be difficult to stand up for yourself, sometimes you do need to escalate the issue if people are not abiding by the agreement. Having emails to support your claims is so helpful.

Thank you for sharing your life and I wish you all the best in grad school!

❤❤❤❤

Jaquie changed my life! I have been chronically ill since October 2012, she was the first chronic illness youtuber I followed, I loved her content, I was subscribed to her and even become a patron! I was in the midst trying to get a diagnose of my stomach problem and she told me to keep fighting for an answer and because of her I GOT DIAGNOSED! I now ALWAYS say positivity is the way forward in life it's something like she said but its something I stand by now! When she passed away I was heartbroken and reading online what they said about her husband. She did NOT deserve the hate she got she was SUCH A GOOD PERSON! I used to spread awareness and share my journey on my IG and one woman "claiming" to be chronically ill was stealing my content by rewording my posts and posting them on hers I have since stopped and this woman closed down her IG after people called her out for faking turns out she actually was which is sickening!. RIP Jaquie you are deeply missed :(

Your skin is glowing, love it. I get this feeling too, despite being diagnosed with all these illnesses doctors and therapists say I have. It doesn't help that those in my life have been invalidating about them. But of course they have.

Congratulations! It sounds like this is something you wanted to do and you've done a great job preparing for it. I'm happy for you! I definitely want to keep up with your vlog series here.

Hey I have a similar story. I have bipolar and ED too. I binge when I have money. What I've decided to do is spend all of it on groceries and healthier foods (some junk as well but no seed oils as they trigger manias in me). I also have a lot of supplements I take to keep my issues at bay. I don't want to advertise my channel or videos at all, but I want to help you. If you are curious, I have one on curing my mental issues (by cure I mean get to the root cause and fix it, which is genetic so no true cure). I hope you check them out. Take care. You're a beautiful soul, as many of us bipolar people are. :) Love you.

Skin Grip makes a cover/over-lay to help reduce the chance of the Libre 3 falling off. I use the Skin Grip Max cover. They are about $24.99 for a package of 10 on Amazon. The regular Skin Grip is also about $24.99, but comes in a package of 20.

Thank you! Many disabilities/chronic illnesses are DYNAMIC. Have gotten so much crap from people who get upset because, “I saw you last week and you looked fine!” Yes, Karen… and then I worked the concession stand at the school dance the other day & it kicked my a$$.

I remember you said you have bipolar. I do too. What do you take for it? I take OTC lithium orotate 20mg, 10mg twice a day morning and evening. Just started three days ago. Manic and depressive episodes are getting better already.

Very glad you got out of that horrible lifestyle. I was a vegan for like 4 months. It was horrible. I lost all my muscles.

How are you doing after the gallbladder removal?? are you back to normal?

Maybe you should take some clips from Chronically Jaquie and other UA-camrs that are disabled and show those clips and show some posts on Reddit side by side and show how this subreddit has and is doing harm but show how these UA-camrs are not faking it and how they are really disabled and how by this subreddit can hurt an individual? Great video. I know that I would love to see this subreddit disappear forever. Because of this subreddit, I know that many people with disabilities have been afraid to do things they needed to do for fear of being blamed for faking their disability. For example, let's say someone has CP but if the person doesn't have a look or the symptoms that are listed in the doctor's textbook then that person may not get the medical care they need or if something is not spot on they may not get the diagnosis they may need? Thank You for your video.

Have you ever gone out to a venue for example a Jazz basketball game and let's say they say "No outside food or drinks" and you are not able to eat the food they sell at that venue? Let's say you are going to other places after the venue you are going to and you have one of those Ensure's or snacks that you pack with you. What does the ADA have to say about that? I am legally blind and I use a power chair and on a low fixed income. I do have GO and IBS. Can you please make a video on these issues?

I know I am disabled myself and I have some disabilities that are "undiagnosed" meaning that they are not in the medical textbook like Cerebral Palsy is in the medical textbook. When Illnessfakers on Reddit are allowed to exist it hurts disabled people and really can not only hurt people who have diagnoses that are in the medical textbook but can hurt people who don't have a diagnosis. I would love to see a video where people can expose the people who post on Reddit and how to shut down the subreddit Illnessfakers? I have had people in real life call me a faker and I have had people deny me service and help because they thought I was not disabled because someone else believed I was not disabled. We need to find a way to really around getting the subreddit shut down? I love Chronically Jacquie videos. I wish she was here still?

I also love how anytime anyone offers the tiniest criticism, they get massively down voted and accused of being the whoever illness fakers was bullying at that moment. I was banned because Jackie posted a few pics of her glucometer during hypoglycemic episodes, and everyone was saying that she was in the "normal" range and was lying about being diabetic. I'm type one diabetic, so I pointed out that the "normal" range is for people without diabetes, but anything under 80ml/dl is considered low and needs to be corrected with food. I was accused of being Jackie (never even followed her) and spreading "false information." I've only been dealing with this for 27 years, so what do I know about keeping myself alive 🤷‍♀️ Not even the poor woman's death has convinced them that she was actually sick. They maintain that she messed with her feeding tube in order to obtain more sympathy. 🙄

I’m getting my gallbladder out in a week. I HATED the second part of the HIDA scan… I did get a diagnosis of biliary dyskinesia and a 29% ejection fraction