This Disease Changed My Life - My Ulcerative Colitis Story

[@Kephinio]

I’m not deaf or anything, but I really enjoy your videos. 😊 Thank you for this story! I don’t want to cone off as rude but this makes me so glad I don’t have this disease. Hopefully a solution will be found. Have a great time!

[@fluffykoala711]

Scuse

[@mentarim3170]

So true

[@lucym22]

@@fluffykoala711 ???

[@buseboskurt8233]

-- that was not rude but you may hurt her feeling by saying that.. I'm sure she doesn't want to have this disease either-nobody will want to deaf

[@beepsta]

-- ok imma be real. How?

[@nevaehbobbi]

Hi, i'm deaf Wow youre so amazing and you're so brave through your harder life. Can't believe you didn't give up and thank you for share this story. I'm interesting it ❤️❤️

[@Bunny2319b]

Heaven backwards👀

[@melonsings5122]

This girl needs a million subscribers ❤️❤️

[@faedraarias278]

Yes I agree

[@hneybba7103]

Vhj GHjj true

[@jeremiahclark4721]

YES!

[@KatTheLavaGirl]

Agreed

[@Sasyta007]

It is so amazing the way we all humans find a way to communicate and move forward, absolutely love your channel and the overall idea of it💡♥️🤗

[@mrsdecelles]

I’m deaf myself/American and I’m also diagnosed with Crohns!! However it’s remission now (thank goodness!!) and I’m really glad you shared your story and it’s so nice knowing there’s another deaf lady who also going though same as me! However your experience seem more severe than mine!!! HUGSSSS

[@amandawesley580]

Try contacting Dr folonsho, he Is a herbal doctor, he healed me from UC, this disease is really terrible, I can only feel what you are going through now

[@haleymay44]

my mom has actually struggled tremendously with Crohns her entire life. I actually witnessed her experiencing a flare up once when i was 13 and it was a really scary experience to see because she thought she was going to die. Diseases like this seem to make life so extremely unpredictable and scary. I hope one day a cure is found. Thank you for sharing your story Jazzy! I am a recent subscriber and I love all of your content(:

[@annikaw3506]

I have Crohn's and I just want to thank you for sharing your story and spreading awareness. Your openness has inspired me to be less embarrassed about my disease.

[@annikaw3506]

Also what is the steroid they put you on with "no side effects" please? I'd like to ask my doctor about this.

[@JazzyWhipps]

@@annikaw3506 They're called Cortiment. Hope this helps!

[@mrsbumfluff836]

My son has pan ulcerative colitis. He’s 21 now and it started when he was 14-15 he was in agony every night, he couldn’t sleep and when he used the toilet it was like he was passing strawberry jam( I know it’s not nice but that’s how it looked). He lost 3 stone in a couple of months. He couldn’t eat. Doctors kept telling us nothing was wrong and he probably had piles until one night we had to rush him to hospital, he was in agony. And like you he was kept in hospital for a week and had so many tests including colonoscopy. We were so scared he was dying because of the pain he was in and how Ill he looked. He’s on medication for life too and like you has good days and bad and can’t eat just anything he wants to. If I could take it away from him and have it myself I would. Thank you for sharing your story, it’s so similar to my sons. It’s just not talked about or understood enough. I don’t think people realise how bad it is x

[@cao0323]

This may seem odd but even though you aren’t making any sound I can still tell you are British lol

[@brattpunzel4706]

Same. As soon as I saw her I just got the British vibe. Also when she's whispering or when she uses her implant to hear herself speak, you can kind of hear her accent.

[@controversy4987]

Gisselle Diaz You can’t hear an accent from her, because she never probably developed one. Accents are developed after you grow and learn how to pronounce words in a country. Just letting you know.

[@brattpunzel4706]

@@controversy4987 yeah well I didn't ask, have a nice night 😗

[@controversy4987]

Gisselle Diaz No need to be a smart ass, I just stated facts.

[@brattpunzel4706]

@@controversy4987 first off idc if you were stating facts and second i wasn't bein a smartass im just generally a mean person and that's how I talk and respond to everyone no matter the situation. That's me as a person. Thank you have a good day.

[@mjcdub8871]

THE AMBULANCE NEVER CAME THAT IS FREAKING RIDICULOUS!!!!!!!!!!!😱🤬

[@xtaebear8071]

IKR!! THATS SO RUDE OF THEM!!

[@katerijayne2668]

It’s not just unacceptable, it’s illegal. Emergency services are legally obligated to show up.

[@xtaebear8071]

Kateri Jayne wdym? We NEED services!!

[@Teknikah]

@@xtaebear8071 It happens in the NHS unfortunately. The service is so unbelievably stretched. I completely agree that it's 100% wrong and everyone who needs an ambulance hsould get one. But say 100 people all need transport to A&E all around the same time, and there are 50 ambulances, they physically cannot get to everybody. I work in a Doctors and we called blue light for a patient we had with us, and it never turned up for us either. They did tell us when we called that they had an unusually high demand at that time. This just makes me fume about the time-wasters that think it's funny to phone 999 saying "omg, my dad has stabbed me" and get an ambulance to rush out as they run away laughing because it's a hoax

[@WILL_DPW]

Yeah, I thought my sister accidentally overdosing on meds, when the ambulance took four hours to arrive, was bad

[@katiem2686]

I can’t imagine how you’d feel during this awful experience! I don’t have this disease but I understand about depression I think you are very brave to share your experience ❤️

[@kirstenstokes7913]

I have Crohn’s disease. Got diagnosed in 2017 but was going to the doctors for 3 years before that with weight loss, unbearable pain, running to the toilet and they just told me it was irritable bowel syndrome or it was in my head. I was being hospitalised for blockages in my small bowel every couple of weeks and was really poorly. Finally one doctor listened to me and said it didn’t sound right and sent me for a colonoscopy. They said it was severe crohns. Ulcers the whole way through my digestive system from mouth to rectum. Was finally put on strong meds to help it and was feeling better for about a year and then they told me in March 2018 I needed surgery to remove the stricture in my small bowel. 30 cm of my bowel was removed and was in hospital for 3 weeks. This disease is awful but you are such an inspiration, I love your videos. Keep up the good work x

[@Tentacl3mommy]

Kirsten Stokes this is exactly what’s happening to me now. I’m finally going to be sent for a colonoscopy, but until recently it’s like no one wanted to take me seriously.

[@crooked7592]

I've never had Colitis but I've had Appendicitis, but that doesn't sound even close to as bad. Thank you for sharing this story, it opened me up to the very serious issue that this disease is causing. I really hope they find a cure! you're amazing, keep up the great work!

[@jamesohehir5728]

I understand how you feel jazzy. I have ulcetative colitis too. Thank you for sharing your story you have just earned a subscriber

[@Sasyta007]

Anyone else trying to focus on the hand movements, face expressions and captions at the same time?? 🤣😭 I would read but miss the actual expression of the sentence and then I’ll focus on her and lose track of what’s happening 😂😭😂

[@sophieb3955]

Isabella Villalobos I do that

[@Teknikah]

That's sign language for you :) I'm hearing but I'm learning BSL and you have to watch hand shapes, positions, facial expressions and lip-pattern all at the same time. It can be hard

[@muskanbhatia242]

Hey Jazzy, I am very sorry to hear about your awful disease. This story made my heartbreak. My goal is to live a life without any kind of disease. Yes, I am praying for you to get well soon. I hope there will be a cure sooner or later. By the way, I am hypochondria. You are an inspiration! Thank you for sharing this disease.

[@mia-tr1ks]

Hi Jazzy! I’m new to your channel, but you seem like such a lovely and positive person! I am so sorry you had to go through all this; it is just TERRIBLE!!! I really hope they find a cure soon. You are so inspirational for going through the disease and still carrying on with normal life. Keep on being amazing! ~ ❤️🧡💛💚💙💜🌈✨

[@JasmineVlogs]

I just love watching you sign💕 I’m from Britain too, but I moved to Australia and I’m studying my masters in mental health. You’ve really inspired me to learn sign language! You’re such an inspiration to not only the young viewers, but for the older ones too! Keep doing what you’re doing, we love you 😘

[@jae-ds2ot]

This really inspired me to start learning sign language for a classmate He is super lonely and is completely mute and deaf and his hearing aids bearly help I love your personality because it shines through even in sign language

[@sunnydayze2306]

My boyfriend has IBD (crohn's)💩 and he has a stoma now, his was too bad for any medication to work so they had to remove all of his colon and some of the small intestine too! he has to give himself injections now to keep the crohn's calm💉 hopefully it will work! Thank you Jazzy for talking about this, I'm sure it will help lots of people💖

[@amandawesley580]

After my chrons disease diagonisis 8 years ago, I stopped all the chrons disease medicines/treatment prescribed due to severe side effects, and decided to go on natural herbal approach. My primary care provider introduced me to Dr folonsho and immediately started on their chrons disease herbal formula treatment, this herbal treatment made a tremendous difference for me. my symptoms including shaking,diarrhea,vomiting,blood stool,fatigue,abdominal pain,stomach pain,excruciating pain and urinary retention all disappeared after the 1 month treatment contact Dr folonsho the herbal healer { { [e-mail]} you can visit his website at drfolonshoherbalhome.simdif.com/ order-online -today

[@dmacxo]

Was watching your videos as i come from the siri vid. Was so lovely to come across this one. I have an ostomy bag due to a rare birth defect but many of my ostomy friends are in the ibd community so thank you for being open about it as it must be hard! New sub here ❤

[@jackmacdonald3229]

Hey Jazzy! I too have Ulcerative Colitis and I'm currently learning BSL as I have some friends who are deaf and I really want to be able to comfortably sign with them 😄 you're awesome, keep doing what you're doing, much love 💛

[@P1P2P3_59]

Thank you for sharing so bravely. Made me feel less alone with my IBS!

[@makaylajrichards5866]

I have only been watching your videos for no longer than a week but you have truly inspired me! After watching your first video i subscribed without even thinking and I don't regret it. Continue to do what you love and know that we as fans are here for you. Love you!!

[@sofiamaldonado8034]

You are so strong! Thank you for sharing your story.

[@theodorageorgescu305]

In June 2013, I've gone through the most excruciating pain I've ever experienced. After years of eating only rice at every meal and seeing multiple doctors, I found out I was suffering from IBD. It's been a hell of a ride, but what helped me recover was reducing the stress level. Emotions play a big role in our body and they affect the digestive system if they go bananas. So please, keep in mind: you come first! Take care of your mind, body & soul!

[@user-dm7xe4ty1y]

I’m not deaf but I really enjoy your videos. Also idk if you are doing the captions or not but whoever is doing the captions is amazing! Your very funny and I like to read the captions

[@matildemendespinto8642]

Your video with Siri was in recommendated videos and it was the best recommendated video KZbin as recommendate to me in a very long time :) You are so strong, and you're so inspiring, even for people like me who are not deaf !

[@crooked7592]

thats actually how i found this channel as well :) This channel is great

[@conflictpersona8]

Im glad your family is so supportive and thank you for sharing your experience. Thankfully your second batch of steroids was a little less traumatic. And you really gave a better understanding for me of these diseases.

[@katiegeorge3824]

You’re a true trooper. Honestly such a brave woman❤️❤️

[@rdeka]

I also have a deaf younger sister 😊 our bonding is same like you and your older sister have.. I'm very happy to see that our family is not alone the world has many other families like us

[@melaniehayes2756]

Brilliant Jazzy, really interesting to hear your story and share awareness of Inflammatory Bowel Disease ❤️❤️

[@sevans1414]

Thanks for making this video Jazzy, I learned a lot of things about bowel disease I didn’t know before! Some people are uncomfortable talking about this stuff (ie poop haha) but it was refreshing to see you just say it because it’s important for people to know about these diseases. I hope the steroid helps even more!

[@W1kster]

I love your videos literally, the time your with people but want to watch KZbin and cba to get your headphones! Well your videos save me

[@jasminsander-jackson8719]

Stay strong you’re amazing and beautiful 💗

[@biaazalmeida]

You’re so brave for living with this illness every day, I hope you have lots of “ups” on your colitis from this day forward!!

[@melsdems9434]

Hey I have Crohn’s disease and I can say my experience from the disease to the treatment was the same just different dates, it’s good to know I’m not alone, thanks for making this video.

[@ccatherinechang]

Everyone will stand up for the deaf. I am so grateful for you to finish fighting off the pain. I never knew that the people’s reasons or what happened to get your deaf was now over. I am your biggest fan and supporter towards your bravery.

[@Lilothestitch]

I’m not deaf or anything but I enjoy your videos. I’m sorry you went through all of that and I hope there will be a cure for this disease.

[@lemonsprout8705]

*me looking for content* *me finding this* Me: looks interesting Me 10 seconds later: idk sign language :( Me two minutes later: *gets sign language classes for next school year* :]

[@musicaddict8470]

Girl just turn on the captions! It tells you what she is saying..! 😑

[@lemonsprout8705]

Cloudy Sweets oooh didn’t know u could do that

[@lemonsprout8705]

Cloudy Sweets I still struggle with reading tho 😂

[@musicaddict8470]

@@lemonsprout8705 it's fine! 😂😂

[@lemonsprout8705]

Cloudy Sweets thanks for telling me 😂

[@stuartthomson2846]

This sounds awful, glad you pulled through and able to share your experience with others, hopefully brings more attention to this disease! Keep up the good work :)

[@louloubieberful]

I recently just found your channel and I immediately subscribed!😁 I have IBS-C! I'm really happy you made a video talking about your journey to a diagnosis, you are beautiful and my inspiration😊❤️

[@dawntreader2420]

I found you through learning ASL with my kids. I'm so glad I found you because I have Crohn's! (Oh, IBS also.) I'm so pleased to find a video with signs specific to my (our) medical issues. Thank you for being open about your health & sharing your journey. I feel incredibly blessed to have found you. I like seeing the differences h similarities between ASL & BSL. There is so much content out there, but not a ton about specific medical conditions. I'm still a Newb, so I probably haven't found it yet. Lol. I really appreciate your video about 10 reasons to learn sign language (not the correct verbiage, I think). That was the first of your videos I found.

[@sammocha]

I was about to be like “why don’t I listen to this to this while I fall asleep?” And then I realized that I needed subtitles...

[@dexa6623]

Thank you for speaking up about this. Normally people aren't very open about digestive issues, because they're seen as "yucky" topics, but untreated, they can be incredibly dangerous. And I hope there's better treatments, or a cure as soon as possible, because that sounds incredibly difficult to live with.

[@amandawesley580]

After my chrons disease diagonisis 8 years ago, I stopped all the chrons disease medicines/treatment prescribed due to severe side effects, and decided to go on natural herbal approach. My primary care provider introduced me to Dr folonsho and immediately started on their chrons disease herbal formula treatment, this herbal treatment made a tremendous difference for me. my symptoms including shaking,diarrhea,vomiting,blood stool,fatigue,abdominal pain,stomach pain,excruciating pain and urinary retention all disappeared after the 1 month treatment contact Dr folonsho the herbal healer { { [e-mail]} you can visit his website at drfolonshoherbalhome.simdif.com/ order-online -today

[@fiski5789]

!!!! ahhh im glad to have found another person in the community, hope youre well!

[@ellepoynton935]

Crohns is common in my family, my uncle has it and is in hospital now, sadly having to have a bag and also my great aunt has it too so when there’s anything slightly wrong with bowels in our family the doctors (and our family) are always like OKAY BUT CHECK THIS AND MAKE SURE THIS IS OKAY because we know what can happen with it when it’s undiagnosed for a long time. I can’t imagine what you went through and how scared you must’ve felt, I wish you all the best now and hope that you’ve got a better handle on it now at least? At least you got a cheeky holiday to Spain😉😩

[@Imamotherfreakingavocado]

I love your videos I can't understand sign language but I want to learn it and these videos are helping me a lot so thank you

[@roroc9732]

Paige Mogan you can turn on captions

[@rebekahsoccasions6691]

You are so pretty. thx for this story! have a great day!

[@emilyt4907]

My mum has Crohns and colitis too. Hers was really bad last year and she lost alot of weight and nearly ended up in hospital. She started infusions which really helped! As my mum was so poorly we didn't do anything during half term last year. My mum also hopes one day there will be a cure. I helped my mum alot when she's in a flare up. My mum told me I'm very understanding and she doesn't know what she would do without me or my sister.

[@soupdavud]

Yo, Im deaf too and in England I have IBS + migraine in seven months It was rough days because school and GSCE Become I was depressed so much because IBS made cutting my food and feel not hungry. But IBS colpermin pill helped me so much better than before... Feeling better now ahah Thank you for your shared! ❤️

[@australianrebornnursery4313]

Rumplestiltskin_x I have had IBS ever since I could remember it’s really awful isn’t it. I hope you are well 🌷

[@kathrynandersonmusicallover]

I have ibs too and I hate it and after I feel like I have got one health problem or something under control another problem arises! I hope you are both doing well?! :(

[@Websty]

People who dislikes have no respect!! Liked the vid

[@beno3366]

EcHo Websty maybe they simply did not enjoy the video?

[@sxilormxrzz5117]

I'm not a deaf person But I have been practicing sign language that way I can help people that are deaf. Your story inspired me to practice sign language that way I can always be prepared and help people whenever I can.😊

[@shir600]

I enjoy your videos so much you are too cute and real with us!! ❤️❤️❤️

[@SteamBugVin]

Thank you for sharing your story. My youngest nephew has chron's and it has been a lot for him and the family to handle. It's nice to see that he isnt alone on his experience. I'm so sorry that all that happened though.

[@fantabulous3825]

You are a very strong person! Makes me think how grateful I am for everything, absolutely love your videos, so here’s a new subscriber ❤️

[@marilynbouziane5530]

You're such an inspiration for all of us, you're a sweetheart.. And by the way, when you zoom, you remind me of a character in sesame street cartoon, it's a her, I can't remember the name.. Very funny.. Keep up the good spirit..

[@georgie-leighanntaylor5811]

OMG this video I cried!! 😥 your really brave and amazing❤

[@gracechang4074]

hey, I think your story is very inspiring thank you so much for sharing with us♥️ also you’re absolutely GORGEOUSS and you give me motivation to work and live harder in life because often times I get so ungrateful or entitled without even knowing,, so I know now to be grateful more becuz seeing you has inspired me. I also struggle with an illness but it is mental.. it is depression and anxiety. I ofc know that it wouldnt compare to what you had to or have to go through, but I can at least asure you you are not alone. And I support and love you and there are people for you always there. Also I will be praying that there is a cure for this. And this sounds corny but I wanted to be succesful and rich when I grow up, so I will definitely support this disease and similar things for deaf or anyone who needs help with the money. thank you for sharing and keep being you and being strong😍💕💕💕

[@glitterbea]

My mom almost died when her bowel obstructed from her chrons. But thankfully she went into remission with minor ups and downs. I have ibs fibromyalgia and chronic migraine which makes me have chronic pain. I'm hanging in there with you sister! 🙂💗

[@dracomalfoyfangirl6892]

I’m not deaf or anything but I just wanted to say that you are a wonderful person and that are beautiful just the way you are!!!! Edit: I can’t actually read sign language but I find It kinda fascinating no offense !!!

[@njdevfan20]

I can relate to the part of the story when you were in the hospital staring at the wall. I was homebound for ten years. I hope you are having more good than bad days.

[@jackieyundia]

Oh wow, it is a very interesting story to hear that! And I don't have that but I have called Memory it means forget before I start to have a memory when I was 1 year old it is worse ever forget until my grade 5 I start more remember than before. And I am your hugeeee fannnnnn and I watch the whole of your vids.

[@payetonarmstrong]

I love your videos so much my step mom is deaf so I know a lot of sign language and it is such an amazing language and I love learning more and more your videos are amazing you are truly a beautiful girl with a beautiful personality❤️

[@fiena179]

you're so beautiful ! 😍🥰😘 even if ur deaf ure still amazing as u are . don't ever change yourself . im feel sad/happy watching ur videos . it made me think that u should be grateful what god made u . many ppl don't want to have a disease , but god is testing u . so be grateful of what u are . be happy that u are a healthy , happy , normal and more . btw i love ur videos ;-;

[@erikaruth8299]

This is really late but girl, can I relate to constantly wondering when you're going to get sick again. I have something wrong with my stomach (undiagnosed) and gluten intolerance as well. I don't have the bleeding and extreme pain, but boy can I relate to you!

[@kathrynandersonmusicallover]

It could be this condition called irritable bowel syndrome because I have it and I really hurts for me but is different for everyone but yeah, look it up! Hope you get better soon!!!

[@arichuwu3490]

I feel so bad watching this because I watched a movie called “A silent voice” She looks so happy...! I hope you stay good to yourself!!! I think your so brave..

[@anthonyjoyce7946]

Your honestly hypnotic ❤️

[@lucym22]

I had to have my Appendix taken out and it hurt so badly too. I could've died as well if they didn't take it out as soon as they did. Love your channel Jasmine keep going. Xx

[@crooked7592]

The same thing happened for me! It had ruptured. It felt awful, but it sounds like almost nothing compared to what happened to Jasmine.

[@lucym22]

@@crooked7592 I know mine ruptured too. But I had a worse experience because of how long I have to stay in this 1 room for. I stayed for like 5 hours, and they told me I could have the surgery in the evening the same day, so I was getting excited. Then they came back a while later, to tell me that I can't have my surgery today, and that I need to go to another hospital. So they spent another hour or so discussing it, when they finally told us which hospital I'd be going to. Then a while later, I got there and it was literally like 1AM. Bearing in mind that I went to the first hospital at around 3PM in the afternoon. It was not nice. Then I finally had my surgery the next morning.

[@crooked7592]

@@lucym22 Oh dang i had to wait a while but not THAT long 😬 well i'm glad its over for both of us

[@lucym22]

@@crooked7592 yes me too.

[@lunap.7650]

My step mom has Crone's disease, but I never really new what that implicated.... I knew that she had to be careful with what she ate and stuff but not much more... Thank u for this very eye opening video😍😍

[@axeladamazda3319]

I was diagnosed in April, 2013 with UC. Similar situation as to yours. But I had to get emergency surgery because my colon was perforating. I had the ostomy bag for 6 months. Then in 2014 I was diagnosed with pyoderma gangrenosum and they found out I moved onto Crohn's disease. Coming up in April, 2020 it'll be 7 years with IBD, I've got every side effect you can get with ibd lol, I'm happy to see you want to do the walk for a cure, I did it 2 years ago I think and was the honored hero, too. #invisibleillnesses

[@katelyn52000]

Hi there!I am a big fan!I feel bad for you and I hope that you find a cure or something to make it better!You have become very successful and I am so proud of you!Have a great day!😊💜💜

[@karenthomas9966]

Oh wow first all I'm glad u doing alright. Just be strong be faith stay positively 😊

[@jillianeee_13rama54]

When i open my youtube app i always go first in your channel because i love watching your videos and you are so beautiful❤️😍

[@TheDoomsday-ok8pr]

This is amazing! I'm not deaf but I enjoy this. Amazing!

[@MeetThePresleys]

Your adorable love your videos !!!!! ThankYou for sharing !!!

[@Chanhee]

Did you sue for the ambulance not showing up? O.O

[@erikaruth8299]

They should have 😬

[@anjachan]

yeah, I can't believe it o.O

[@kaylimcginnis]

My sister had Ulcerative Colitis. Sadly her story took a much different path. Unlike yours hers never went into remission and they had to remove her colon. Even now she is still in pain from everything. She has had over 10 procedures and is only 14 now. It’s not a fun condition at all. It was so bad she nearly died a few times.

[@faizaali8438]

Hi am deaf and am really excited about your video and I enjoy it I hope you enjoy your happy and life peaceful 😝😝😝

[@claudiamendoza7381]

I have Irritable bowel syndrome... thanks to give importance to this topic, some people think it isn't painful

[@LittlebeanandMe]

You should try and get in touch with Hannah Witton (another British you tuber), she has Ulcerative Colitis - might be a helpful connect!

[@aikachu3903]

Happy b-day! Wish you the best!😊❤

[@hotteaspill5204]

Love u so much !! Love from india!

[@yonglixiepop]

I'm not deaf but I enjoy your videos!

[@ciaraclarke3535]

Omg just found this video! I have ulcerative colitis too, I was diagnosed in 2014, just before my end of school exams, I was 18.

[@bluejamicahoopz4]

Wow 😯!!! It pretty serious and you got better your health again 😊🤟🏾

[@simonadumitrache5933]

😥😥😥 i m sorry for you ,i have also irritable bowel and it affects my life a lot :(

[@australianrebornnursery4313]

I love your videos 💗

[@emmy7125]

In here Siri video I heard a faint sound from her voice she said “understand me” very lightly . Your voice could be amazing

[@davina200111]

When I was born I was sent straight to special care after I had a kink in my bowels. I’ve always been to the doctors & the hospital about it! I’m really bad at taking my medication but the pains are awful! Staying up feeling like you’re dying

[@jinabang2374]

My mom also has colitis and my sister has chronic and yeah.. Hope you get better :)

[@user-zj6wl3ud8u]

Wow I am half deaf and blind I know its harder like this pain and sometimes stress I am new and I love how someone like me is going through like me but I am not alone l, None is alone

[@Matt-tr8yk]

Awesome video! Im deaf Love from Chile

[@jsl4459]

I’m blind ur videos have changed my life I can really understand you

[@haleema0505]

JSL4 uh so if you don’t mind me asking how’d did you understand the video..?

[@duckxlr9245]

I have a friend with cystic fibrosis. She has a tube in her stomach that she has to take out and change monthly. She has to take a vest 2 times a day, 5 diffrent types of pills daily, and her nebulizer 2 times a day, doctors say she will only live until about 30 years old. I think it’s 1 time ever 2 months she gets really sick (well she is very sick but does not act like it) she is in the hospital for 2-3 weeks she has scars from needles and IV’e she is used to not being able to breath, and being sick every day.

[@xxhotramen4666]

Its like a lifetime period

[@aimanmujahid3797]

I’m deaf I feel soo bad for you got this disease it so horrible but also at same time it got really interesting good job you make this video and also I hope you will get better with this disease but funny thing is what when my mood is down or sad I usually watch funny movie it made me laugh and forget it but I don’t know if it will work for you

[@oliodonohoe6546]

Thanks Jazzy, really enjoy your videos. I’ve been living with Colitis for 2 years and was in hospital for 21 days back in March 2022. I’m now on Vedolizumab infusions every 8 weeks, which takes up only one hour in hospital. I have zero blood and totally normal frequency of stools. How are you doing? Oli x

[@jkze8406]

Great Video Love your stuff!!!

[@neenahbenzinger9555]

I love ur videos and I think your an amazing strong brave girl keep doing what you do best l❤️❤️❤️