My grandma had lymes disease but she was never properly diagnosed with it because apparently "there is no ticks that carry lymes disease in Canada." She had the tick bite mark and her symptoms matches those of lymes. It then spiralled into a bunch of other autoimmune disorders and numerous other issues. Thank you for spreading awareness about this and sharing your story.
Your life story is really amazing, you have a lot of strength to face this disease and I admire you because you have managed to overcome your fears and continue fighting for what you want... greetings from Peru and keep going, I have always followed you, I like to see you grow in your projects
You are really a superhero Rose and in the words of British pop singer David Bowie (1947-2016) "We can be heroes, just for one day. " I love you so much and take care Rose. 🇬🇧🇬🇧🇬🇧🇮🇪🇮🇪🇮🇪😀😀😀❤️❤️❤️🌹🌹🌹
Hi Rose thanks for sharing your story, you have been through such a huge challenge, I knew very little about Lyme disease, I'm deeply honoured to hear your story, sending best wishes and safe hugs from Australia
Thanks for sharing this story. Remember that you’re not alone. We’ll be here by your side as you get through this. Wishing you so much love and the speediest of recoveries. From your Japanese fan.
I'm so happy you shared youre experience. I have been trying to do some research on the disease but nothing was giving me what I was looking for. I have learned so much and I love feeling more aware about people's lives. Thankyou
you're so strong for everything especially for making this video. I can't imagine how much pain you went and still going through. If i were you i would probably already give up but you truly are inspirational and once again so strong. We love u Rose❤️
I also have depersonalisation derealisation for my entire life on and off I can really sympathise with you and the fact you’re still laughing and positive is amazing. You’re a strong woman
thank you so much for sharing & trying to bring awareness! when i was in high school many people at my church got diagnosed with Lyme, and many had had it for years without knowing. My husband had Lyme disease as a child but he only experienced symptoms for a short time (maybe a year??) and no longer suffers from it.
I have severe CFS/ME and I literally cannot think of a single reason to get a positive experience about being severely ill and getting my life taken away from me. ME has one of the lowest quality of life compared to many other diseases. I don't want to be anyone's inspiration or have any desire to be strong because of my disease. Imagine the worst you've felt in your life and being trapped in that day basically forever. You get no good days were you feel normal. It's hell through and through. You don't get to socialize, go outside to get fresh air, take a walk or do anything that can give you happiness because happiness can trigger adrenaline and the stimuli of experiencing joy can be too much and you crash feeling like death for days, weeks, months or years. Some people can't even taste food because their bodies are too damaged by the disease and basically lay in bed like a terminal cancer patient on their last days but without dying. Death to all chronical diseases. I'd prefer to be healthy and have my legs cut off than living with ME. At least I could be able to go outside with a wheelchair.
thank you for being so upfront about your illness and experiences. I am 24 and have been chronically ill (Bechterew’s disease and multiple spinal surgeries) since I was around 12. I make art about illness but I am never so upfront about it, because it scares me. I also have known a lot of misunderstanding. It’s safer to be silent - or cryptic, at least. But I realize I owe it to the ill community to not hide and downplay my experience
When I saw you on the news in Australia (I’m Australian haha), I immediately searched you up. It is so good you are using your platform to bring awareness to important things. God bless! ❤️🥰
ok so now i realized that i know what it is i just didnt know it at first because English isn't my frist language but at the same time k didn't know that it's this bad i mostly just heard about it and you talking about it amd explaining it to people so they wouldn't have to go through what you did is just somehow so powerful and amazing that makes me love you even more
Hope you are getting well and full of energy. You're really are the best one who does 70s looks on UA-cam. You do it so smoothly and so beautifully. Please make more videos!
I suffered from a different illness too and I can relate to that pain you feel when people don’t understand what you’re going through… it’s painful.. people will never understand you if they don’t experience that theirselves. That’s okay on some point but prejudice it’s just so disrespectful and hurtful. You’re strong Rose, so proud of you🙏🏼❤️
I’m so sorry that you have had to hear awful comments about your illness from people not understanding what it is like! I myself didn’t know just how severe this illness could be before watching your video. Of course not knowing is not an excuse for people around you or anyone to make awful comments, and you shouldn’t have to take the responsibility to educate them either, but I think there is so little awareness about lyme disease that people just don’t know any better. It’s amazing that you could take your time and make a video about this, even though it’s obviously not easy to talk about, but you’re spreading awareness so hopefully more people will know about this and be kinder and more understanding ❤️ I hope you’re doing well, you’re amazing!
I don’t have Lyme disease, but I do have a disease. So, on that level I do know what it is like to not live a “healthy normal” live. My disease is genetic. My Dad, Grandma, and Great Grandmother had/have it, but my case is the worst. You are in my thoughts always. I have been sick since I was 5, but they didn’t give me a diagnosis (they didn’t have a name) until late 2018. I have had people not believe me when I would tell people or I would not go to school and etc. People reaction like “can I have your life I would love to stay in bed all day” annoys me so bad. Living with a disease does make you enjoy the little things so much more.
Thank you for sharing! I don't have Lyme disease, but the journey of learning about my undiagnosed mental illnesses has a lot of similarities. Feeling like I'm not alone
Thank you Rose for educating me about how Lyme disease can be like, I heard about it but never really learned details about it. I’m following your Instagram too, you’re such an amazing and strong beautiful person❤❤love from Japan
I’m so sorry about your disease, I hope that you get better , you know something? Everytime I see you , you remind me of princess diana and you make me feel that she stills alive and with us helping us and giving us love , 😘😘😘 hope you get better
You definitley have a new Fan now I Do Not have lyme desease but i know what It means like Not being healthy...you are so beautiful inside and out and very strong ....looking forward for more Videos Would like to know more about you Stay strong
Also I'm actually pretty sad that i didn't even know what lyme disease is that's why I'm thankful to you for putting effort on making this video although it's really hard for you
It’s rare I find someone who has such a similar illness journey as me! I don’t have Lyme disease, I have Endometriosis, Ehlers Danlos and a few other things, but we became ill around the same age and had a pretty similar experience with doctors and getting the right diagnosis. I’m 30 now and it’s been a process getting to a point where I’m managing. Still bed ridden most of the time but there’s a lot of little joys amongst the bullshit!
Thank you for doing this. Anyone can make a video talking about beauty, but you actually want to help people and that is admirable.👑 By the way, you might have heard this a lot, but you look a lot like Princess Diana
no bc the way she uses her platforms to spead awareness about stuff like this. Have to love her
🥺🥺
Second for the woman, the myth, the legend Rose Nora Anna.
I'm so proud of you, Rose ♡︎
My grandma had lymes disease but she was never properly diagnosed with it because apparently "there is no ticks that carry lymes disease in Canada." She had the tick bite mark and her symptoms matches those of lymes. It then spiralled into a bunch of other autoimmune disorders and numerous other issues. Thank you for spreading awareness about this and sharing your story.
Your life story is really amazing, you have a lot of strength to face this disease and I admire you because you have managed to overcome your fears and continue fighting for what you want... greetings from Peru and keep going, I have always followed you, I like to see you grow in your projects
You are really a superhero Rose and in the words of British pop singer David Bowie (1947-2016) "We can be heroes, just for one day. " I love you so much and take care Rose. 🇬🇧🇬🇧🇬🇧🇮🇪🇮🇪🇮🇪😀😀😀❤️❤️❤️🌹🌹🌹
Yessir!!
Hi Rose thanks for sharing your story, you have been through such a huge challenge, I knew very little about Lyme disease, I'm deeply honoured to hear your story, sending best wishes and safe hugs from Australia
Thanks for sharing this story.
Remember that you’re not alone. We’ll be here by your side as you get through this.
Wishing you so much love and the speediest of recoveries.
From your Japanese fan.
you‘re so strong. Crazy to know that we went through so much together. So amazing to see how far you‘ve come
I love you so dearly isi😭 you’ve gotten me through so much❤️
@@rosenoraanna i love you too ❤️❤️
Love you, angel! This was so beautifully done. So incredibly grateful to call you my friend.
I'm so happy you shared youre experience.
I have been trying to do some research on the disease but nothing was giving me what I was looking for.
I have learned so much and I love feeling more aware about people's lives.
Thankyou
you're so strong for everything especially for making this video. I can't imagine how much pain you went and still going through. If i were you i would probably already give up but you truly are inspirational and once again so strong. We love u Rose❤️
I also have depersonalisation derealisation for my entire life on and off I can really sympathise with you and the fact you’re still laughing and positive is amazing. You’re a strong woman
Your so strong.. I’m happy and I hope you feel better. We here for you.
You're such a wonderful and strong woman and an inspiration to many!🤰💪🏻💖
thank you so much for sharing & trying to bring awareness! when i was in high school many people at my church got diagnosed with Lyme, and many had had it for years without knowing. My husband had Lyme disease as a child but he only experienced symptoms for a short time (maybe a year??) and no longer suffers from it.
Ugh Rose you are so strong. I am so proud of you for finally make this video! I love you❤️❤️❤️
I have severe CFS/ME and I literally cannot think of a single reason to get a positive experience about being severely ill and getting my life taken away from me. ME has one of the lowest quality of life compared to many other diseases. I don't want to be anyone's inspiration or have any desire to be strong because of my disease. Imagine the worst you've felt in your life and being trapped in that day basically forever. You get no good days were you feel normal. It's hell through and through. You don't get to socialize, go outside to get fresh air, take a walk or do anything that can give you happiness because happiness can trigger adrenaline and the stimuli of experiencing joy can be too much and you crash feeling like death for days, weeks, months or years. Some people can't even taste food because their bodies are too damaged by the disease and basically lay in bed like a terminal cancer patient on their last days but without dying. Death to all chronical diseases. I'd prefer to be healthy and have my legs cut off than living with ME. At least I could be able to go outside with a wheelchair.
Wow! You are so brave sharing your story. I am also glad that you are spreading awareness about lyme disease, I've learned so much from your video!♥
thank you for being so upfront about your illness and experiences. I am 24 and have been chronically ill (Bechterew’s disease and multiple spinal surgeries) since I was around 12. I make art about illness but I am never so upfront about it, because it scares me. I also have known a lot of misunderstanding. It’s safer to be silent - or cryptic, at least. But I realize I owe it to the ill community to not hide and downplay my experience
so excited for that vid girl
When I saw you on the news in Australia (I’m Australian haha), I immediately searched you up. It is so good you are using your platform to bring awareness to important things. God bless! ❤️🥰
ok so now i realized that i know what it is i just didnt know it at first because English isn't my frist language but at the same time k didn't know that it's this bad i mostly just heard about it and you talking about it amd explaining it to people so they wouldn't have to go through what you did is just somehow so powerful and amazing that makes me love you even more
Hope you are getting well and full of energy. You're really are the best one who does 70s looks on UA-cam. You do it so smoothly and so beautifully. Please make more videos!
I suffered from a different illness too and I can relate to that pain you feel when people don’t understand what you’re going through… it’s painful.. people will never understand you if they don’t experience that theirselves. That’s okay on some point but prejudice it’s just so disrespectful and hurtful.
You’re strong Rose, so proud of you🙏🏼❤️
I’m so sorry that you have had to hear awful comments about your illness from people not understanding what it is like! I myself didn’t know just how severe this illness could be before watching your video. Of course not knowing is not an excuse for people around you or anyone to make awful comments, and you shouldn’t have to take the responsibility to educate them either, but I think there is so little awareness about lyme disease that people just don’t know any better. It’s amazing that you could take your time and make a video about this, even though it’s obviously not easy to talk about, but you’re spreading awareness so hopefully more people will know about this and be kinder and more understanding ❤️ I hope you’re doing well, you’re amazing!
I don’t have Lyme disease, but I do have a disease. So, on that level I do know what it is like to not live a “healthy normal” live. My disease is genetic. My Dad, Grandma, and Great Grandmother had/have it, but my case is the worst. You are in my thoughts always. I have been sick since I was 5, but they didn’t give me a diagnosis (they didn’t have a name) until late 2018. I have had people not believe me when I would tell people or I would not go to school and etc. People reaction like “can I have your life I would love to stay in bed all day” annoys me so bad. Living with a disease does make you enjoy the little things so much more.
Thank you for sharing! I don't have Lyme disease, but the journey of learning about my undiagnosed mental illnesses has a lot of similarities. Feeling like I'm not alone
Thank you Rose for educating me about how Lyme disease can be like, I heard about it but never really learned details about it. I’m following your Instagram too, you’re such an amazing and strong beautiful person❤❤love from Japan
You are so strong, thank you for sharing your story! Much love from a fellow lymie 💗
Sending so much love your way💗
@@rosenoraanna You could send your love to me Rose. ❤️❤️❤️🇮🇪🇮🇪🇮🇪🇬🇧🇬🇧🇬🇧🌹🌹🌹🤗🤗🤗😀😀😀
I am so proud of you
めっちゃかわいい！ kawaii😍
I’m so sorry about your disease, I hope that you get better , you know something? Everytime I see you , you remind me of princess diana and you make me feel that she stills alive and with us helping us and giving us love , 😘😘😘 hope you get better
You definitley have a new Fan now
I Do Not have lyme desease but i know what It means like Not being healthy...you are so beautiful inside and out and very strong ....looking forward for more Videos
Would like to know more about you
Stay strong
Also I'm actually pretty sad that i didn't even know what lyme disease is that's why I'm thankful to you for putting effort on making this video although it's really hard for you
I had Lyme disease in 2019 :/
Hope you get better soon ❤️
We all love you ❤️💪
It’s rare I find someone who has such a similar illness journey as me! I don’t have Lyme disease, I have Endometriosis, Ehlers Danlos and a few other things, but we became ill around the same age and had a pretty similar experience with doctors and getting the right diagnosis. I’m 30 now and it’s been a process getting to a point where I’m managing. Still bed ridden most of the time but there’s a lot of little joys amongst the bullshit!
Thank you for doing this. Anyone can make a video talking about beauty, but you actually want to help people and that is admirable.👑
By the way, you might have heard this a lot, but you look a lot like Princess Diana
Love u rose❤
I had lyme disease it sucks
I love your Diana hair
Goodmorning,Rose! I hope your Lyme disease gets cured. Btw,you look just like Princess Diana.
Not related to the video, but I love the Horizon album in the background! ❤️
Love you 🥰❤️
I am proud of you too
Just commenting to engage. I didn't know about it and I feel that people should know too
Her accent makes me think ab fluttering butterfly wings does anyone know what I mean it’s so cute n delicate :))
She reminds me of my role model Princess Diana, she’s so beautiful
Plss make more video huhu
Oil oregano
In Jesus name be healed
The Lord heals
First