This is relatable. I have POTS and Gastroparesis, C-PTSD, IBS, Chronic Gastritis, Cyclic Vomiting and so many other issues. So you are totally relatable!! *hugs* if welcome. You are beautiful and strong and you are doing your best, which is 100% enough!❤
I‘m honestly at a loss for words. You are so incredibly brave for sharing this so openly and speaking up. The fact that you are experiencing all of this and still try to make the best out of every new day is inspiring and eye-opening, to say the least. I wish all the best and am sending you all the love there is. I have rarely seen someone as strong as you are 🧸💕
The way my face went 😦 when you said that there are people who don't "think that gastroparesis can be fatal." I just? Gastroparesis is a very dangerous illness and the fact that anyone thinks otherwise is absolutely bananas to me. Regardless, thank you for sharing! When people are comfortable doing so, it's so important for others to share their experiences and illnesses. It helps others with chronic illness not feel so alone 💕
this took so much bravery to talk about. I'm so glad that chronically ill regressors will have somebody to relate to. You are so incredibly strong and I wish the absolute best for you. Sending my love to you and your amazing caregiver 💖🌸
I feel for you. I have Ehlers Danlos Syndrome with chronic pain and fatigue. Good and bad days. It is what it is. I have undiagnosed GI issues but I try my best to basically eat like I do have gastroparesis since it's a big comorbidity with EDS and it works for me. I also have mental illnesses: ADHD, undiagnosed autism because according to my research and how much I relate it makes sense, major depressive disorder recurring moderate, generalized anxiety disorder, adjustment disorder with anxiety, panic disorder without agoraphobia. I'm glad you have things that help you and the support you need.
I am so glad you exist. Thank you for sharing your story. I hope you know that although your abilities are limited, this little world of innocence and love you’ve created for yourself is like a microcosm of the essence of life itself. It’s that purity that people search their whole lives for, when it’s really wherever we are, inside ourselves. All the wonder in the world can be found in small moments. In a room. In a hug or words of comfort or adoration from a loved one. From laughter . Even just listening to our own heartbeat and breath and realizing the miracle they are. Your heart has touched many and holds a lifetime’s worth of importance. Its impact will be felt generations after you, continuing to protect and bring happiness to others in vulnerable positions. Much love to you beautiful soul! ❤
Hi. I also have Gastroparesis and complex trauma and am diagnosed with Dissociative Identity Disorder and because of that, although I'm 39, I have a few younger alters. So I think that's kind of like age regression. Although I don't really remember or know what I act like when that happens, just what people around me tell me. But people do tend to tell me I tend to act much younger when I experience chronic illness flare-ups. Also I really like your dress. It's super cute. I think it's so brave of you to talk about this. I don't think there is anything you should ever be ashamed of. If age regression is helping you be a person you are happy with and you are not hurting anyone else. Why does it matter? Sending you so much Love and support ❤️
I also live with Gastroparesis, C-PTSD, and Panic Disorder, Ehlers Danlos Syndrome, as well as severe Fibromyalgia. So, I can absolutely emphasize with you. And I agree... it's so very hard sometimes to get people to understand! Countless times I've had people think that I'm Anorexic or something because eating is such a painful process. But, I wanted to thank you for sharing. So many of us live with "Invisible Illnesses", and so many people don't believe in them... sigh. Just, thank you for being brave and open 🤍
My prayers are with you. Trust me, being in chronic pain. Every day is never easy. And those who never experience that will never understand what it's like when your body is attacking its own self. For no reason, accept, that's what it's doing and. It ain't gonna stop No matter what you do! Best advice I can give you keep looking for. The happy beautiful little moment within your beautiful life. Because though pain may run our lives and pain may be something that we have to go through. It does not define who we are. So stay strong fee incredible, just the way you are. Remember that your life is beautiful one.❤❤❤❤❤❤❤❤❤❤
thanks for sharing your story. I share a few diagnoses with you, therefore I am acutely aware of how isolating that "invisible disabilities" can be. your video made me feel less alone
Oh, that is quite a load on your shoulders. Thank you for producing this video since it will help others with the same condition. I am glad you found regression ... hugs to you!
I’m a regressor dealing with pain that renders me unable to walk at all some days. I haven’t found the problem just yet, but I appreciate you for speaking up like this. I will also be praying for your health so that you can live the long and happy life you deserve to! This world needs more brave people like you. God bless🩷
It makes a lot of sense that with the extreme health conditions you have to live with, that what healing/comfort looks like for you also needs to be just as powerful to fight back- so even if age regression seems “extreme” to most, that’s what you need and thank you for sharing how to do it! ❤
Thank you for sharing. I am chronically ill as well and we share some of the same illnesses. If you feel comfortable making more videos about chronic illness and regression that would be nice. :) Regression is one of the few times I feel okay truly expressing and feeling the pain and grief that my illnesses bring. I hope that your health stablizes and you find some relief. ♥️
im so sorry youre going this and i hope you can live a long and happy life. i have ME/CFS too and a couple other things, so i related to this a lot. wishing you well!
It's annoying when people put their view and inputs when they find out you have a disability or illness like they're an internet scientist. I've noticed it's more of a bad habit of curiosity most of the time and they don't know how to ask, so I try my best to be open.
Hi , this is a very relatable video , i was in a similar situation for ab 5 years , thankfully i survived and got better , don't loose hope doctors can be wrong alot of the time and we get new medication and therapies everyday, a word of advise would be that get physical therapy and some sort of movement , whatever type u can , muscle atrophy happens fast and can make things worse
i am sorry to here about your illness and i can not imagine what you are going though right now and i hope the doctors can do same thing for you and i hope you are doing ok and i will say a prayer for you please get better soon because youtube would not same with out you
this actually is way relatable!! you are not alone in your struggles babe. i have the same issues exactly!! it's rough out here, but at least we all have each other ❤
I'm dealing with fibromyalgia and array. And the weak communion system is never fun. So here's 2 staying, positive. Being fearless and cherishing every single moment on the face of this Earth. Set that way when you look back on your life. You can say I did that and even if you can't do it now. You can still say you did that. Stay strong and remember. Kindness is key to a good life and yourself. Well, thank you for it, and so will those around you😊❤❤❤❤❤❤❤❤❤❤❤❤❤
I’m so sorry you’re going through this. You have a very comforting presence and a beautiful soul. I don’t know what your religious beliefs are, but I will pray for you. I’ve seen God work miracles on sick and injured people, I hope he will do the same for you
Came here from instagram. Always liked your cute pjamamas. Didn't know you had a youtube, also I wasn't aware about your illnesses. Hope your doing well.
I am also a chronically ill little! I use agre on noght im in pain due to having juvenile rheumatoid arthritis and around my cycle i deal wth pmdd which is considered disabling. My body always hirts and being little get me through it alot aswell as helping my mental health amd healing from taruma and years and years of sbuse. Thank you for sharing your story. You are amazing!
Right when you said this is probably not relatable, is when I found it so relatable. I don't have a chronic illness so I am not saying I know what thats like because obviously I cannot understand what that is like. But regression is the only way for me to really feel my feelings instead of just thinking them, regression is the only way for me to feel loved and worthy. Its the only way for me to feel "the heart" of the deeper emotional pain from all of the Trauma I have experienced and not just all the coping side effects fear/panic/anxiety/paranoia. Regression allows me to be as I am and it allows me process.
You’re so precious. Even though we are about the same age, I wish I could take care of you. I would try my best to caress,protect and comfort you. I never felt like that before. You’re a smart,intelligent, super cute, beautiful and kind human being. Also extremely strong. You kinda remind me one of my friends, and I showed your picture to her lol. She had the same opinion about you as I do. I hope life will get a bit easier, and comfortable for you. I know it’s easy to say, but don’t forget to smile, to have fun. Life only makes sense, if we are happy.Enjoy the sunshine,animals and flowers around us:( That’s the only thing that actually matters. I know I don’t fucking make sense lmao but anyways..Every time I pray or manifest, I will think about you! Love you my little girl!🩷🐰🌞🌷🌧️
This is relatable. I have POTS and Gastroparesis, C-PTSD, IBS, Chronic Gastritis, Cyclic Vomiting and so many other issues. So you are totally relatable!! *hugs* if welcome. You are beautiful and strong and you are doing your best, which is 100% enough!❤
I‘m honestly at a loss for words. You are so incredibly brave for sharing this so openly and speaking up. The fact that you are experiencing all of this and still try to make the best out of every new day is inspiring and eye-opening, to say the least. I wish all the best and am sending you all the love there is. I have rarely seen someone as strong as you are 🧸💕
Came here to say this pretty much. You are such an inspiration. Thank you for sharing your light with us!
The way my face went 😦 when you said that there are people who don't "think that gastroparesis can be fatal." I just? Gastroparesis is a very dangerous illness and the fact that anyone thinks otherwise is absolutely bananas to me.
Regardless, thank you for sharing! When people are comfortable doing so, it's so important for others to share their experiences and illnesses. It helps others with chronic illness not feel so alone 💕
I’m so so sorry that you’ve been dealing with ablest comments on UA-cam.
this took so much bravery to talk about. I'm so glad that chronically ill regressors will have somebody to relate to. You are so incredibly strong and I wish the absolute best for you. Sending my love to you and your amazing caregiver 💖🌸
As a regressor that is chronically ill, thanks for sharing 🫂💕
I feel for you. I have Ehlers Danlos Syndrome with chronic pain and fatigue. Good and bad days. It is what it is. I have undiagnosed GI issues but I try my best to basically eat like I do have gastroparesis since it's a big comorbidity with EDS and it works for me. I also have mental illnesses: ADHD, undiagnosed autism because according to my research and how much I relate it makes sense, major depressive disorder recurring moderate, generalized anxiety disorder, adjustment disorder with anxiety, panic disorder without agoraphobia. I'm glad you have things that help you and the support you need.
I am so glad you exist. Thank you for sharing your story. I hope you know that although your abilities are limited, this little world of innocence and love you’ve created for yourself is like a microcosm of the essence of life itself. It’s that purity that people search their whole lives for, when it’s really wherever we are, inside ourselves. All the wonder in the world can be found in small moments. In a room. In a hug or words of comfort or adoration from a loved one. From laughter . Even just listening to our own heartbeat and breath and realizing the miracle they are. Your heart has touched many and holds a lifetime’s worth of importance. Its impact will be felt generations after you, continuing to protect and bring happiness to others in vulnerable positions. Much love to you beautiful soul! ❤
Hi. I also have Gastroparesis and complex trauma and am diagnosed with Dissociative Identity Disorder and because of that, although I'm 39, I have a few younger alters. So I think that's kind of like age regression. Although I don't really remember or know what I act like when that happens, just what people around me tell me. But people do tend to tell me I tend to act much younger when I experience chronic illness flare-ups. Also I really like your dress. It's super cute. I think it's so brave of you to talk about this. I don't think there is anything you should ever be ashamed of. If age regression is helping you be a person you are happy with and you are not hurting anyone else. Why does it matter? Sending you so much Love and support ❤️
I also live with Gastroparesis, C-PTSD, and Panic Disorder, Ehlers Danlos Syndrome, as well as severe Fibromyalgia. So, I can absolutely emphasize with you. And I agree... it's so very hard sometimes to get people to understand! Countless times I've had people think that I'm Anorexic or something because eating is such a painful process.
But, I wanted to thank you for sharing. So many of us live with "Invisible Illnesses", and so many people don't believe in them... sigh. Just, thank you for being brave and open 🤍
I'm hoping your chronic illness gets more manageable. Thank you for sharing your story with all of us. Sending you much love.💕💕
My prayers are with you. Trust me, being in chronic pain. Every day is never easy. And those who never experience that will never understand what it's like when your body is attacking its own self. For no reason, accept, that's what it's doing and. It ain't gonna stop No matter what you do! Best advice I can give you keep looking for.
The happy beautiful little moment within your beautiful life. Because though pain may run our lives and pain may be something that we have to go through. It does not define who we are. So stay strong fee incredible, just the way you are. Remember that your life is beautiful one.❤❤❤❤❤❤❤❤❤❤
I think this is more relatable than you think. Tysm for sharing
thanks for sharing your story. I share a few diagnoses with you, therefore I am acutely aware of how isolating that "invisible disabilities" can be. your video made me feel less alone
Oh, that is quite a load on your shoulders. Thank you for producing this video since it will help others with the same condition. I am glad you found regression ... hugs to you!
I’m a regressor dealing with pain that renders me unable to walk at all some days. I haven’t found the problem just yet, but I appreciate you for speaking up like this. I will also be praying for your health so that you can live the long and happy life you deserve to!
This world needs more brave people like you. God bless🩷
It makes a lot of sense that with the extreme health conditions you have to live with, that what healing/comfort looks like for you also needs to be just as powerful to fight back- so even if age regression seems “extreme” to most, that’s what you need and thank you for sharing how to do it! ❤
Thank you for sharing. I am chronically ill as well and we share some of the same illnesses. If you feel comfortable making more videos about chronic illness and regression that would be nice. :) Regression is one of the few times I feel okay truly expressing and feeling the pain and grief that my illnesses bring. I hope that your health stablizes and you find some relief. ♥️
im so sorry youre going this and i hope you can live a long and happy life. i have ME/CFS too and a couple other things, so i related to this a lot. wishing you well!
sending you the best of luck
It's annoying when people put their view and inputs when they find out you have a disability or illness like they're an internet scientist. I've noticed it's more of a bad habit of curiosity most of the time and they don't know how to ask, so I try my best to be open.
Hi , this is a very relatable video , i was in a similar situation for ab 5 years , thankfully i survived and got better , don't loose hope doctors can be wrong alot of the time and we get new medication and therapies everyday, a word of advise would be that get physical therapy and some sort of movement , whatever type u can , muscle atrophy happens fast and can make things worse
i am sorry to here about your illness and i can not imagine what you are going though right now and i hope the doctors can do same thing for you and i hope you are doing ok and i will say a prayer for you please get better soon because youtube would not same with out you
i love you sweet sweet girl. stay hopeful, hope can cure your soul. hang in there, we all believe in you. thank you for your story ❤️
thank you so much for sharing ✨ my space feels very similar, and I think you're more relatable thank you think 💙
this actually is way relatable!! you are not alone in your struggles babe. i have the same issues exactly!! it's rough out here, but at least we all have each other ❤
I'm dealing with fibromyalgia and array. And the weak communion system is never fun.
So here's 2 staying, positive. Being fearless and cherishing every single moment on the face of this Earth. Set that way when you look back on your life. You can say I did that and even if you can't do it now. You can still say you did that. Stay strong and remember. Kindness is key to a good life and yourself. Well, thank you for it, and so will those around you😊❤❤❤❤❤❤❤❤❤❤❤❤❤
I’m so sorry you’re going through this. You have a very comforting presence and a beautiful soul. I don’t know what your religious beliefs are, but I will pray for you. I’ve seen God work miracles on sick and injured people, I hope he will do the same for you
" I LOVE YOU "
Thank you for sharing, I know it takes a lot of strength and courage to do this, I just thank you so much. Sending you love 💕🎀
Came here from instagram. Always liked your cute pjamamas. Didn't know you had a youtube, also I wasn't aware about your illnesses.
Hope your doing well.
I am also a chronically ill little! I use agre on noght im in pain due to having juvenile rheumatoid arthritis and around my cycle i deal wth pmdd which is considered disabling. My body always hirts and being little get me through it alot aswell as helping my mental health amd healing from taruma and years and years of sbuse. Thank you for sharing your story. You are amazing!
Right when you said this is probably not relatable, is when I found it so relatable. I don't have a chronic illness so I am not saying I know what thats like because obviously I cannot understand what that is like. But regression is the only way for me to really feel my feelings instead of just thinking them, regression is the only way for me to feel loved and worthy. Its the only way for me to feel "the heart" of the deeper emotional pain from all of the Trauma I have experienced and not just all the coping side effects fear/panic/anxiety/paranoia. Regression allows me to be as I am and it allows me process.
GBY, Hon! I appreciate U sharing.❤
Thank you for this video ❤
hope your okay
Keep the good work, stay positive.
Your very pretty
You’re so precious. Even though we are about the same age, I wish I could take care of you. I would try my best to caress,protect and comfort you. I never felt like that before. You’re a smart,intelligent, super cute, beautiful and kind human being. Also extremely strong. You kinda remind me one of my friends, and I showed your picture to her lol. She had the same opinion about you as I do. I hope life will get a bit easier, and comfortable for you. I know it’s easy to say, but don’t forget to smile, to have fun. Life only makes sense, if we are happy.Enjoy the sunshine,animals and flowers around us:( That’s the only thing that actually matters. I know I don’t fucking make sense lmao but anyways..Every time I pray or manifest, I will think about you! Love you my little girl!🩷🐰🌞🌷🌧️
sucks that you have to deal with all this ableism
I wuuuuuuuuuuuv the buley water bottle im gay
one of my ablist friends took control of my account Im so sorry baby. I am assuming the role as your cg ;00000000000000000
I seriously hope that these disabilities aren't due because of the C19 injection. I hope that you didn't took it, hope your suffering gets lessened.
covid 19 injection doesn’t give people those illnesses 🤦♀️
booooooooo
@@catfreestyle No, but it can make a lot worse previous pathologies in the body. There are now published medical research papers about this stuff.