Chronic Illness TikTok Compilation 4
Вставка
- Опубліковано 9 вер 2024
- Chronic Illness TikTok Compilation 4
_____________________
Get Fidget Toys at low costs and fast shipping at
Syco Fidget Store - bit.ly/3lm1Ydp
we hope you guys enjoyed this compilation!
Don't forget like this video and subscribe to our channel for more tik tok compilations!
Our Mail - tiktoksomer@gmail.com
Love the constipated woman's honesty and ability to joke about it. Happened to me once so bad I had to be admitted to hospital because the build up in my intestines pressed so I couldn't pee. My bladder was about to burst when they inserted the catheter. I was so embarrassed and it was an awful experience but she made me feel more able to laugh at it.
that happened to me when i was really young i was born like a month early and i guess there were something wrong and the first 2 years i always got sick, wouldn't sleep and in one case couldnt go to the bathroom i don't remember it thank goodness but i heard it was pretty bad
I used to be the exact opposite of constipated but my diet and medication recently has made me occasionally constipated (happy 1 week w/o pooping!) and what usually does it for me is a few bowls of grapes but everybody’s body (and intestines) are different.
I have really bad constipation from my chronic illness and tbh I cannot joke about it like that so props to her
I’ve had this happen to me once and had to get an enema.
I once got super constipated. They thought I had kidney stones because I was in so much pain. Turns I needed to poop and I couldn't because I was dehydrated. Lol
A lot of people don't seem to understand that as much as we want to be waste free having a or multiple chronic conditions means you often can't. I need disposable needles, syringer, test strips, urine dip sticks, inhalers, medication packets, vials of liquid meds etc. I know how the first girl feels my digestive system packs up without strong daily meds and 4 sachets of laxatives per day xxx
That’s so true I have cystic fibrosis
@@tommarvoloriddleakavoldy9263 it's so difficult and people keep saying waste free is easy not for us its not! Xxx
@Amara Ezeoke no but I can relate to the struggle of certain green initiatives not covering those with chronic illness xxx
I can relate because I have Fanconi anemia so my DNA went wack and changed a little bit and made me a sick person that needs pills and an injection every day. Whenever I go to school kids always tease me or bully me because I'm smaller (Fanconi anemia can make it's victim's smaller than a usual person).
Just think how much money there is in the development of Green biomed products. You'd think someone would be interested in providing the materials that can save someone's life WHILE saving the planet.
To the girl who had POTS and googled and diagnosed herself, I’m proud of her for not letting the doctor tell her she’s “too young” and stuff like that because (even though this isn’t a chronic illness or even close what you guys have to go through) when I was 10 years old I literally went on google and diagnosed myself appendicitis and sure enough what did I have? Bro just because we don’t have a degree doesn’t mean we’re dumb. Also I just googled my symptoms and I apparently have a chronic sinusitis so yea
I have anxiety and a eating desorder (nutritional issues) I have to say that is difficult to me to eat because i always feel vomity my doctor saids its normal but I know its not, but thanks God I'm blessed and I know someday I will eat normally and I hope everybody be good too
google isnt the same as a doctor
For those that don't know, rubbing alcohol with help remove the sticky adhesive in tapes and bandages on your skin without pulling a ton and making your skin irritated as heck (I mean if it still is you're likely sensitive to adhesives which talk to your doctor they can give you a less irritating kind!) If you peel a tiny portion up then kind of wiggle a cotton pad damp with rubbing alcohol under the edge as you peel it(like right up against the tape while holding your skin down gently) seriously saves you so much frustration and pain and prevents you ripping the hairs on your body off as well ❤️ best wishes to all going through daily life with chronic illness
so will a lot of oils. Had open heart surgery and definitely had many sticky adhesives left. We used oil and alcohol to get them off.
Really? I thought they were using remove wipes (that remove the glue) because I literally can not get take off my adhesives with alcohol. My skin gets all red and sometimes I bleed. Am I just sensitive? 😭
There’s also some sprays but not they aren’t easy to get 😕
That and goo gone I use that when I have adhesive on my arm from my dexcom
i always had really bad constipation since i was a toddler
thankfully it hasn't happened in a long while, but I'm really happy it never was as bad as the girl in the video
I’ve had constipation since I was 3, and it’s all my babysitters fault for not letting me poop for 6 days cause she couldn’t be bothered to get my potty out. I hate her so much-
@@kaleidoscope773 | oh my god that sounds awful, what the hell is wrong with her
@@Sammers7 Idk, she was always horrible to her kids and the kids she babysitted- but yeah laxatives don’t even work for me like the girl in the video and I’m too scared to get an enema ;-;
@Mia Sosa | yea i think its more common when you're young, but some people get lucky and not have it or at least not have it as bad as others
I am in my teen years and I have severe constipation since covid 19 started, took my a year later for them to tell my it was just constipation and now I have to take miralax and Beni fiber every day till June. Yay :(
11:28 i had a diabetic friend at First grade and when She had to measure her sugar rate the teacher would pause the class and let her measure It, i remember we counted until twenty when She had her insuline shots and we even had a palestry explaining diabetes at that same year.
She was at my School until fourth grade i guess (im bad in remembering things lol) but we talk to still this day.
122 and she faints!?! I’m up here sitting at 160 and I’ve never fainted. It’s so wild how everyone’s body handles pots differently.
I have pots and only ever FEEL like fainting, I have never fainted tho
I have POTS and faint so often :c I think a large part of it (at least for me) is the blood pressure dropping alongside the tachycardia
I was at 240 at on point and I felt really dizzy but never faintes
My heart went to 170 yesterday as I was walking up the stairs. I think I may have pots, I have all the symptoms. My mom won’t let me get tested even when I offered to pay for it
I need to get tested for pots, I either get really dizzy or I faint for a few secs, but trying to get a damn diagnosis where I am is insane
Damn doing those tube things up your nose looks so awful.. these kinds of videos make me realize how lucky I am to be healthy and not have to do those things
They're honestly not that awful once you're used to them tbfh. Although it also depends on which type you have.
The only super bad thing is when they get snagged which fucking huuurrrttts
@@emmb9306 I have a question if that's ok, do you have to wear it 24/7 and what is it for?
That’s kinda rude but ok
@@unnathivarma2043 I'm not the best person to ask since ive only ever had a tube a few times. Typically, theyre used for people who cant eat, cant absorb nutrients by eating or for people who dont eat. I have extremely bad acid so i had the tube for a while to help let my throat heal from the constant acid reflux and another time was due to a medication i was on making it hard for me to swallow. Everyone is different though.
@@Kassia_G_ what's rude? The person asking that question? Its not rude and if anything, its good that they're wanting to learn
I have a handful of chronic illnesses/disorders. My list (at least diagnosed ones) includes severe anxiety and depression, OCD, ADHD, Ehlers Danlos Syndrome (connective tissue disorder), psychosis, and Neurological Lyme Disease. I have trouble doing the basic tasks of living, and the only reason I got diagnosed with anything was because my mom has most of the same things and I pushed to be tested. And, the ones she doesn't I Googled symptoms of mine and pushed, despite being told that I'm just a kid, and I can't diagnose myself from Google. Moral of my rant, if you have suspicions about things like this, get tested. I know I'm very lucky to have been diagnosed between the ages of 7-12, because this kind of thing is hell to be diagnosed with only when you're an adult. Thank you for coming to my TED talk. :)
Hi :) I (kind of) know what it's like. (Not intending to be rude) because I have a lot of chronic illness. My list: Anxiety (social and separation) and depression, adhd, autism, spd, selective mutism, ehlers danlos syndrome, and an eating disorder and type 1 diabetes. Hope your doing OK :)
Having my stomach become paralyzed is one of my fears. I haven't been diagnosed because I've never brought it up to my doctors but my throat gets paralyzed at times and I am unable to swallow. It's scary because it's happened with liquids too and when I told my parents my dad said his mom had problems like that.
please let a doctor know this information! It might not be that serious yet but it could be very serious. you'll never know the extent without having them check it out ❤️ sometimes it's a simple cause other times not but having difficulty swallowing shouldn't be ignored hun, I'd hate for you to hurt yourself
@@erinbanana22 Thank you for the kind words. I will let my doctor know in my next appointment. 💙
Can you still swallow saliva when this happens?
The depression finger thingy is true I’ve been diagnosed with severe anxiety and depression, always talk to somebody about it and they can find ways to help
I was diagnosed with both depression and chronic fatigue which is really hard to deal with. Depression tends to be badly handled by outsiders who haven't struggled with it before and my chronic fatigue is even worse because people just say "well you eat and sleep so there's no reason for you to be tired" or "you just don't do enough exercise". So yeah, I totally get it when people say that no-one understands because my family just says, and I quote, "just get over it".
@@eleanorcooke7136 my mum has chronic fatigue
I'm so glad I've had good experiences with doctors. I was able to get diagnosed really easily because I had done my research into what I might have had and I told my doctor. She said ok and then checked me out as well as checking for a few other things. She thought I had it and sent me to a rheumatologist where I told her the same thing and after a couple more checks and a little more blood testing I was right and I have fibromyalgia. Technically since I'm a 16 it's AMPS, or amplified musculoskeletal pain syndrome. But it's the same thing. I'm glad they actually listened to me.
Sure you do
@@chance2413 I'm also pretty sure that you've got about half a brain cell functioning and even then it's struggling.
I’m 13 and my knees and hips dislocate all the time ( extremely painful) and I can’t even run or go upstairs because my knees hurt so bad… NOT a single docter had been able to figure it out :( a couple said I needed pt and I have been doing it for 6 bloody years another few said it was from lack of OMG IT JUST CLICKED OMFG OMG IT JUST BLOODY CLICKED I’m allergic to like everything so maybe my body isn’t getting the right nutrients to support my joints 😱😱😨😨😨especially because I’m allergic to everything… OMG HOW DID THE DOCRERS NOT EVEN CONCODER THIS
@@Kayla_equestrian Hi friend, your experience sounds similar to mine... I am 28 and I finally found a doctor that heard my weird symptoms and then asked if I have stretchy soft skin or joints lol well, I actually am hyperflexible and it turns out I do have extra stretch to my skin. He was a rheumatologist and offically diagnosed me with fibromyalgia, but also expects I have Ehlers Danlos Syndrome, which is a collagen disorder that impacts every person unique so is hard to identify and they call us Zebras. I'm still learning about it myself, but how you describe your symptoms fits with some of mine and what I'm reading. Remember that you are strong, and not alone. Start writing down your symptoms now, all the things that seem unique about your body experience. I can't tell you how many times I've been like "that's a symptom??? But... that... I've always had that." And when you go to the doctor *have your notes written on paper that you leave them for their notes*. This is something I've only learned recently, by having doctors who didn't take notes, and thus didn't leave a trail of my reported symptoms. Take your healthcare into your hands, it is the only way to get good care too often. Blessings of love energy from Oregon
10:26
Off topic but I am legit obsessed with her nails
Thank you for sharing it means a lot. I thought I was the only one who had bowel movement conditions and honestly my meds are putting me in the dark. I’ve been stuck with it since I was 6 weeks old and I’ve been hospitalized 3 times and I now have life long trauma due to my condition...
"These are all symptoms of depression"
Me being diagnosed with chronic Extended depressive disorder: *Bruh*
dude same lets gooo
@@featherlesstriped9817 At first I was like "Wait what did I comment?" and then I saw the comment and just started dying LETS GOOOO
Sameeeeee
Ticked all the symptoms and now I'm wondering if I should get myself checked out...
I ticked off 7...MDD
"be careful because once I took one packet and shat myself at work" 3:28
I love how she uses comedy to get through the bad times 😅
It took me two years to be diagnosed with pots even though I was a textbook case and every doctor I went to asked if I had been tested. But it literally took two years for one of my doctors to actually test me when I told her I hadn’t t been tested yet.
This is why I’m literally scared to ask my doctor about running tests.(I think I might have pots or something like that, not trying to self diagnose but damn I have a lot of symptoms) Last time I mentioned feeling dizzy and having black spots in my vision she just ordered blood work😕
Took me 5 goddamn years to get diagnosed because " You're to young to have POTS" and " You're diabetic it's probably your blood sugar."
wait a moment im sort of early that is cool
Here's your medal 🏅
Same I’m 3 weeks early... that’s a new record
@@kevinfightsbears * steals medal *
@@oliviahizon8974 can't relate
@@oliviahizon8974 im 4 weeks older
Lol I remember when I was constipated and I hadn’t pooped in 1 1/2 weeks so I took laxitives and stuff after a 1 week of not pooping and then I went to a sushi restaurant with my friends and I got miso soup, soba, and fried oysters and i tell you I have never drove home so fast in my life and anyways I was on the toilet for like 3 hours
I am not one of the ill, but I love watching these to help be more aware! I hope you all are doing well and recover/have a better quality of life!
The tik tok at 4:01 is actually really reassuring to hear cause literally my mom constantly mad me doubt my depression even when suicidal and tho I'm being treated now and is feeling better I'm still seseptable to all these things randomly happening. Feels hella good to know I'm not some chick doing this for attention.
6:21 This makes me really happy to see- I've had lung issues since I was born and I've been on daily steroids for a fairly severe case of asthma since I was seven years old. I've had a nebulizer at home since I was two, and in my off season I'm on it several times a day. I'm seventeen years old, and somehow, I've never seen anyone with a nebulizer in any media, even on one of these compilations, until now!
Seeing videos like these means alot to me. My younger sister has chronical illnesses and has to be fed thru a tube. I was always worried she'd hate herself growing up. But knowing she's not alone and hoping she'll see these videos one day brings me hope that she'll be okay.
Oh man the poop ones. I feel them on such a personal level. Idk what exactly is wrong with me BC I can't afford a doctor but I've had those same experiences too many times. It's really awful. Don't take pooping for granted.
Maybe you got crohn’s like me 😎 I get free medical insurance from Pennsylvania
M o v e t o e n g l a n d f r e e h e a l t h c a r e
Feel the constipation pain. I'm really prone to it but one time when I was eight I got really constipated and it took six months and very severe pain before they finally figured it out. I take laxatives regularly but still have lost of problems with it. The nature of having severe constipation is very hard because people don't usually think its bad and it really gets hard sometimes. I also have a relative with a rare autoimmune condition that is like less lethal version of MS. Most people assume there drunk when they first see them because they stumble around, have droopy eyelids, and slurred speech. They have never been drunk and only tried alcohol once. It can be hard because they have finally gotten off most of the treatments but they just stopped the progression so they still have the same severity they did before.
Dude MS is not lethal.
I relate to the first one. I have IBS and Ulcerative Colitis and I have so many issues and it's very uncomfortable but I like how she makes jokes about it. That makes me feel better as well.
Covid tests ain't got nothing on these powerful kings and queens
I just saw this and want to mention this-
I have POTS, and am sooooo happy that there are tik told about this! I was told that most people don't know about it and can't recognize it, but I was lucky to be diagnosed quickly. I am now getting a service dog for this and my PNES.
Even though it doesn't look like I have a disability (more than the two mentioned) I still do.
I have PNES too and i doo faint a lot too honestly it sucks
I can relate to almost all of them. I went through a lot in the past 12 years of me alive on earth and its hard but who ever relates too just know that we’re all on this together!
I used to do infusions. Didn’t work. Took tons of meds. Didn’t help. Changed them. Didn’t help. Now I’m on humera. Finally, after over eight years, I’m getting better. ❤️
It’s nice to see I’m not alone. Granted wouldn’t want anyone to go through this but it’s nice to see people who get it
Completely agree !
0:34 me having scoliosis and having to wear a medical brace for 23 hours and mental problems: Why y'all see us like that as if it's fake...It's real and it really REALLY hurts...
I have scoliosis aswell, I’m just really lucky that they found it when I was a child
@@lambsauce8031 sanaol 😔✊
@@yoisheeshee8376 honestly I hate physio with a passion, years of it is not fun. periodt
@@lambsauce8031 I have to wear it until I'm 18 T^T and fr it is not fun
@@yoisheeshee8376 oh I’m so sorry! My degrees were just under but I got to wear one for a week and I couldn’t bear doing it until I’m eighteen! Thoughts and prayers
6:29 ❤
I have Common Variable Immunodeficiency AND asthma and the amount of times I've been told "ONLY these people will die" re. Covid was too upsetting to talk about, or make a tiktok.
I was on tiktok for 2 weeks and never mentioned my illness but was bullied off for "being an old woman moaning"
I'm 28, so I'm old.
Thank you for being so brave young people. ❤🦓
Us old people are right behind you cheering you on.
Thank you for being so outspoken. 💕
The first girl got right to the point. Lol. I love each of yall for sharing part of your personal life. Stay strong!!💓💓
The ones with the feeding tube are so sad to me because my grandpa had had 3 or 4 strokes then he ended up with a feeding tube and shortly after he died I was only 8 when this happened I am now 10 and miss him so much.😭😭😭😢
Having a chronic illness is one of the hardest things in the world. I have to deal with hydradinitis supertivia, which is a skin disorder that causes tunnels of cyst to form all over my body. Holes that are a half an inch in diameter and an inch deep on my skin. It is painful like a gunshot. I sleep all day to take away the pain. It’s nice to see other people who have to do the same as me and go through hard things but are still productive.
Everyone is so brave on here to be sharing their stories, so I think I’ll share mine. I am 19 years old and I have to use an oxygen tank most of the day, especially when I’m asleep. I also have to give myself injections twice a day since oral medicine I can not stomach at all, which we might end up switching out for an IV at night, sadly, since my body can’t retain most liquids or medications for long. Most of this is resulting from a stroke I had a few years back which we still don’t know the cause of, I can walk just fine thankfully and I’m still alive which is what I’m thankful for, my husband helps with my shots, and you cant even imagine how many sharps containers we have around the house, We know that whatever happened with my lungs was a result of the stroke AND the fact that since I was 3 I would stop breathing in my sleep. Though I’m happy I have my husband to help me through this, and help me with all of the medical things we have to deal with, I love him very much and I don’t know HOW he manages to deal with me 😂 he’s amazing honestly and I don’t know what I would do without him 💕
I was having a hard day/night but you guys make me wanted to be a better nurse, thank you for btightening my day, I promised you that I will get a better nurse as I can for you guys, I don't know if you can read this but if you have a chronic disease I'll blessed you so that you can feel better. 👏👏👏👏👏👏🙏🥰
Although people might have disabilities most people are proud of what they are nothing can bring these people down and that’s what I love. And they are so positive about everything nothing can put these people down.
is it just me or do other people's emotions seemed to have turned off? like i dont really get sad when i should be and im not happy when i should be, but i used to be. i usually just get mad a lot when something tiny bothers me
Same
@@mammonsheep373 club?
@@hannahmontana4401 ya
4:01
Its tiring pretending to be happy. To busy reminiscing on the past, feeling anxious to talk to people, hiding it from family and making sure no one knows how you feel, its tiring.
I watch these videos to relate to people
and it also helps me feel like I'm not alone so thank you for make this video :)
Literally felt that diagnosis with POTS one. I have PCOS and it took me SIX YEARS to be diagnosed because I was told all my problems were a faze, would sort out, women just had that, there was nothing they could do etc only when I demanded a test, which they said would be unhelpful, did I finally get diagnosed.
I’ve had IBS all my life.
It’s no way to live it sucks and yes my relationship with food is “ I’m not sure if I can trust you because last time I was sick “ I have trust issues with food. Parties and events where food is going to be is anxiety ridden!
When you put all your fingers down for the depression one-
I had six down
Ill have all fingers down for sure 🖐😔
I had all fingers down 🖐😭
@Minxxx yeah, I wanted to twist my neck, fall, or jump out of a window.🥴
@@jujubeez7326 don’t fall down at a tall building. It’s very painful it feels like your skin is about to rip off but it actually won’t
Seeing people who relate to me is kinda comforting
I feel it. I have been having panic attacks and think I have deppresion thanks for sharing!
The first one sounds horrible :( I can't believe people go through so much
Anyone else here diabetic? That SUCKS,like imagine having a lifetime of needles finger sticks and a constant risk of dy!ng from passing out, coma, or simply de@th.
4:58
Me with all 10 fingers down: holy shiiiii-
Also me: I mean not that surprising…
Hey!!! I have an NJ tube and have been on it for a while. This tiktoks have managed to get me thru a tough day of pain and nausea. Thank you!!!!!
Did the girl 💩??
This is ridiculous you should be able to buy a enema.... My grandpa didn't tell but he got more than 1 week without 💩 and he had a blockage he was throwing up his 💩, we had to send him 600km away to make another surgery!
You Can buy enemas, but they're often extremely unsafe to do yourself.
@@emmb9306 insert squeeze discard the bottle wait what you can and go tho the throne..... Be happy....
Why is enemas unsafe?
@@JoJohXD let me see if i can explain it decently; AT HOME enemas/OTC enemas are unsafe. Especially if you dont know what youre doing. Yes, you poop out of your butt, so i understand thinking that it doesnt matter if things are clean or not when going uo there but it does matter. Often, the enema kita come with unsterile equipment and/or enema liquids that are unsafe. Your booty hole can and will absorb things and will do so quickly. Thats why we have pills you can put up there.
Also if you dont know how to properly do things, you can cause more damage. You can possibly rupture/cut something and hurt yourself. People get objects lodged in their butts daily and often need surgery.
@@emmb9306 geez i know people do desperate things on desperate times, but this is awful.... Just a nutritionist that deal with people who are constantly constipated, but I never saw the "gone wrong" way! WTF.....
I had this issue, and couldn't stomach eating anything. Then i had miso soup. Felt like i shat my *brains* out after that.
4:56 I just had a genuine panic attack because I got bpd and if I got depresselion and I had all my finger down
As someone with multiple chronic conditions, i love these.
Plus guess who finally just got officailly ffiagnosed today!!
It's nice to see people with a chronic condition too 😅
I have a feeding tube in my stomach instead of my nose so I feel
Really Seen when I see people set up there pumps.
Also having to take out my tube every 2 months really sucks
11:37 I get that a lot too I’m type 1 diabetic so I need to eat something the teachers says give it u can’t eat in class and I say no I need this do u realize that I go into a seizure then they just walk away
I love watching
So I suffer with severe abstract sleep apnea 💔 it makes me really tired and yea no one knows I’m fighting with it. I’m getting surgery next month so yea after surgery I get to be in the intensive care unit (ICU) in case i stop breathing 😗🤌 life is just fun with sleep disorders
Update- after surgery:
I fell better but yea I still struggle to sleep and yea
I like this video so much that I watch it everyday
these people are so brace to be able to share this on the internet, bless y'all 🙏
Due to Covid, EJ had a huge panic attack where he physically couldn't move, his dad wasn't helping either, that's when Daniel, Amber and Alex first turned up. Covid is also a problem for those with bad anxiety and other mental health issues.
Who else has a sensory processing disorder 👀
Me
@@ghosti_vx5342 :D
8:29 is so relatable.. just got diagnosed with autism and inattentive adhd (add) at age 19 after being told by one of my old psychiatrist that I "dont look or act autistic "...also doctors need to stop saying "it's all in your head" and then using that as grounds to do nothing for you. Umm it's a mental illness,,, of course it's literally all in my head... I would know!
These girls are so good at replacing their feeding tubes. I admire them. Having had to use them in the past,a medical professional always had to reindeer them because there's a danger of them going into your lungs. Well done ✔
At 6:23 I have that condition it is called CF and I affects your lungs and I am constantly in hospital.
Im so glad theres people sharing this stuff. Ive got CFS (still in the process of being diagnosed properly since its not a diagnosis that can be given in itself and every doctor i went to wrote it off as being my depression worsening for 2 years. Like... yeah, that, too, but its not just bloody depression.) And its not nearly as bad for me as what some of the people in the videos or comments have to deal with daily, but it's still really exhausting to deal with (pun intended-) since im 16 and noone really believes me. My mother rolls her eyes when i bring up that im sure i have it, and until recently doctors wouldn't even listen to me and refer me straight to a psychiatrist that wouldnt really take me seriously either. I use a cane sometimes because i dont feel strong enough to walk more than a few hundred meters on some days. Im still getting used to living with it even after two years, but ill be going back to school (after half a year of abstinence) in february. I hope it goes well.
The depression one with the fingers
Me being diagnosed with depression for over 2 year and haveing all my fingers down
...god damit these people are psychic
4:02 I- I put all my thinkers down...
This used to happen to me but I was really young I was in the hospital for three months. I’m sorry for what you are going through. It’s been hard for me too but we can get through it together.
9:47 She Has All the same symptoms I had and have taken all the same medications I’ve taken before,
And turns out I have celiac disease and allergic to eggs, soy, and dairy😩 I really hope she can use the bathroom soon rn I’m struggling too stay safe everyone💖💖
I have all the symptoms of depression.
I have severe depression, but i still push through and try to do things i used to love, most of the time its boring but i like it sometimes.
Anyway, have a good day!
Can you post more chronically I'll tiktok compilations plz I'm chronically I'll and love watching these
I have POTS as well and at 9:04 I understand the struggle, I got told the exact same exact things and I knew something was wrong and my mom came across pots when her doctor mentioned it. So we went doctor to doctor until we finally got diagnosed with, POTS. I wish doctor would actually listen to you and do their research rather than tell someone that they are crazy or stressed. I am 11 now, and we started looking for a diagnosis when I was 8. Please listen to your patients and help them instead of hurting them with those words.
7:32 damn that was so graceful compared to my episodes- i stumble and hold onto a chair for dear life and then call out for my parent(s) or a friend if they’re near
I have a chronic illness, but I can actually call myself healthy now and it is so hard remembering not being healthy...
The first thing I here when I play the video
I CANT POOP
In which country you get a heart range monitor and infusion for depression?
I went to a lot of mental hospitals in Germany and I never once saw a treatment like that.
Normally they just gave out pills over pills and let ppl play boardgames.
It must just depend on what the protocol at that hospital is. But she could have an depression related ed or could be dehydrated bc she isn't motivated to drink water or something else.
Lmao the first one had me tho 💀 I love how she can just openly talk about something like that
4:11 I am literally trying to do Spanish but I am watching this while doing my Spanish at 12: 57 in the morning
i feel so sorry for these people but i am also proud of them for not letting these illnesses spoil their humour
These tiktoks are so interesting to watch especially when they're relatable.
--------‐-‐‐-‐-------------------------------------------------------------------------------
There were so many complications in my birth and I almost died. My mum was in labor for 2 weeks until the nurses finally believed her when they found my poop inside her and manually broke her water for her. When I was little I started having trouble pooping and went weeks without, I was tested for celiac but wasn't yet on solids so results came back negative, when I was on solids they tested again and it came back positive. When I was a toddler I was in hospital and being fed through a tube. When I was young and in school I couldn't run, whenever I would run I would start to cough and had to stop because I was breathing so fast, now whenever I do even a tiny bit of exercise my heart beats crazy fast and I have to slow down and sometimes I need to use an inhaler because I have trouble breathing. My hayfever made my nose runny and I had to take eyedrops because my eyes would kill me. I had really dangerously bad iron deficiency and had to take daily iron tablets because I would refuse to eat. My eczema was really bad when I was younger behind my knees and elbows, it faded into really dry hands and what I'm left with now is rarely having dry hands, knees, elbows or even having my neck be itchy at times but I can't do dishes or wash cars without being itchy from the soap. Excessive urination, thirst and blood sugar of what showed up as not having a reading because it was too high then a reading of 33 or 34 mmol helped identify my diabetes. I have celiac disease since I was pretty much born, asthma for as long as I can remember, eczema as long as I can remember, hayfever somewhere between 8- 10 yrs old and Type 1 Diabetes at 12.
I’m gonna cry a person in this had POTS…. me too… aaahhh it’s nice to see some people have it!
These all look terrible im am so sorry to people that have to go through things like this like i was a sickly child but never as bad as this
I used to have blood cancer and it was very hard for me only being 3-7. I had a nose tube and I would have the feeder thingy too. I hope you all have a good day
Lol lately ive been wondering about my physical being and not my mental health. Ive noticed when I stand up i get really dizzy and need to sit back down. Ive collapsed a few times but no fainting. I was standing at my kitchen counter today and my brother (who is 11 months old and cant walk) comes over and tries to pull himself up on me, as babies do. He hit the back of my knee and i fell *hard* onto the ground. It was so sudden and loud it scared the literal shit out of him.
All these people are so strong, I can’t imagine having a chronic illness.
4:02 these are all very true coming from someone with depression.....it also feels empty...
Where’s my Hypothyroidism and hashimotos people?😌✨🤟🏻
Ayyee
@@emmb9306 ayyyooo
I’m a type 1 diabetes, hasimotos, Celiac disease, pots, type person
FRESH OUT THE MENTAL HOSPITAL mood lmao
On the lady with chronic constipation, have they tried magnesium citrate because that could help
My brother has a feeding tube and it's nice to see others have the same issue
My 1 year old niece has Holoprosencephaly its when the brain fails to divide properly into the right and left hemispheres and she was also born without a nose and top lip and she is blind which is a lot for a baby and i pray to god every day that something bad DOESN’T HAPPEN because I can’t take seeing my sister sad and I don’t want to lose my baby niece❤️🔥
I have a few chronic illness I have juvenile idiopathic arthritis and I have scoliosis and I have had 2 metal rods pit in my spine (scoliosis), I have had 8 plates put in both my legs(arthritis), I have got some of my rib cages missing, I have almost half of my lings missing. Due to my arthritis (I'm young ~ not much younger than 20) I have had to have at least 15 injections to get rid of bubble things out of my legs (didn't work) and my ankle. Over all I have spent at least 72 hours of surgery maybe more -not altogether-
11:44 it's true it kinda sucks poeple be like I'm jealous of you you get sweets and I'm here like I'm sick of jelly baby glucajuice and most things sweet I guess that sounds great to you
My sister and I have gastroparesis and will eventually need to be on a feeding tube. This seriously SUCKS for many reasons but the two that concern me are 1. We are both allergic/sensitive to adhesives like the tape used to hold the tubes in place and 2. I'm uninsured and the stuff used in place of normal food is VERY expensive.
I am crying and I can't stop- LOL help
Shout out to those who are out there battling these illnesses all the time every hour of every week❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️
I have been depressed for the past 2 years and when she said put a finger down for things and at the end she said if u put all those fingers down its depression! I had again had a mental breakdown
As a victim(not really a victim, just don’t have a better word) of a chronic illness (Type 1 Diabetes) this made me smile a ton.
If you mix laxatives with water and it still doesn’t work try orange juice it really does help actually I don’t know why but it does and taste better