![Villainari_](/img/default-banner.jpg)
- Видео 191
- Просмотров 75 556
Villainari_
Канада
Добавлен 13 ноя 2016
Find me on all my socials linktr.ee/villainari
My name is Ari. My life forever changed in 2008. I am a two time cancer survivor. My health digressed. I was diagnosed with Raynaud's, Perniosis, Ehlers Danlos, postural othrostatic tachycardia, and mast cell disease.
I am not my diseases. I am a survivor, a rare disease fighter and I live with invisible illness. My channel is about me and my journey and how disease tries to rule my life, but I continue to be resilient.
I aim to bring awareness to diseases and create a space for chilling and healing. Art has been the thing which has always been there for me and I want to share my creativity and encourage others to keep chasing their dreams. Going after what you love is vital to survival while living with illness.
Check out my channels
youtube.com/@villainari_fortniteow2?si=1Hy_Dy_1YlHkDxXu
youtube.com/@villainari_art?si=s29mm1MHkD197BKg
youtube.com/@villainari_horror-dt3uf?si=LRIRxo1XaFGcFVL_
My name is Ari. My life forever changed in 2008. I am a two time cancer survivor. My health digressed. I was diagnosed with Raynaud's, Perniosis, Ehlers Danlos, postural othrostatic tachycardia, and mast cell disease.
I am not my diseases. I am a survivor, a rare disease fighter and I live with invisible illness. My channel is about me and my journey and how disease tries to rule my life, but I continue to be resilient.
I aim to bring awareness to diseases and create a space for chilling and healing. Art has been the thing which has always been there for me and I want to share my creativity and encourage others to keep chasing their dreams. Going after what you love is vital to survival while living with illness.
Check out my channels
youtube.com/@villainari_fortniteow2?si=1Hy_Dy_1YlHkDxXu
youtube.com/@villainari_art?si=s29mm1MHkD197BKg
youtube.com/@villainari_horror-dt3uf?si=LRIRxo1XaFGcFVL_
Body Temperature issues with MCAS
**Please note this is not to be used as medical advice, Chronic Heart 2 Heart is a Podcast where people with complex, invisible diagnosis share their stories with the internet. It is simply a podcast of information sharing and caring**
This is a call to anyone in the community who has mental health diagnoses/chronic health conditions or who is considered to be disabled, if you or anyone you know would be interested in being interviewed for my RUclips channel and sharing about your life with your diagnoses please message me I would love to have anyone wanting to participate in my new podcast Chronic Heart 2 Heart.
Posting new podcasts at least once a month for now due to the documentary film...
This is a call to anyone in the community who has mental health diagnoses/chronic health conditions or who is considered to be disabled, if you or anyone you know would be interested in being interviewed for my RUclips channel and sharing about your life with your diagnoses please message me I would love to have anyone wanting to participate in my new podcast Chronic Heart 2 Heart.
Posting new podcasts at least once a month for now due to the documentary film...
Просмотров: 25
Видео
Find it within you The Happiness You seek
Просмотров 11Месяц назад
Please note this is not to be used as medical advice, Chronic Heart 2 Heart is a Podcast where people with complex, invisible diagnosis share their stories with the internet. It is simply a podcast of information sharing and caring This is a call to anyone in the community who has mental health diagnoses/chronic health conditions or who is considered to be disabled, if you or anyone you know wo...
I am so exhausted having to advocate myself
Просмотров 40Месяц назад
Please note this is not to be used as medical advice, Chronic Heart 2 Heart is a Podcast where people with complex, invisible diagnosis share their stories with the internet. It is simply a podcast of information sharing and caring This is a call to anyone in the community who has mental health diagnoses/chronic health conditions or who is considered to be disabled, if you or anyone you know wo...
I am not your inspiration corn
Просмотров 54Месяц назад
Please note this is not to be used as medical advice, Chronic Heart 2 Heart is a Podcast where people with complex, invisible diagnosis share their stories with the internet. It is simply a podcast of information sharing and caring This is a call to anyone in the community who has mental health diagnoses/chronic health conditions or who is considered to be disabled, if you or anyone you know wo...
Chronic Heart 2 Heart Podcast Episode 8 Chris MCAS Story
Просмотров 257 месяцев назад
Chronic Heart 2 Heart Podcast Episode 8 Chris MCAS Story
I don't want Cancer Again Bone Marrow Biopsies
Просмотров 148 месяцев назад
I don't want Cancer Again Bone Marrow Biopsies
Chronic Heart 2 Heart Podcast Episode 7 Fiona Mastocytosis
Просмотров 168 месяцев назад
Chronic Heart 2 Heart Podcast Episode 7 Fiona Mastocytosis
Chronic Heart 2 Heart Podcast Episode 6 Piper Interview Fibromyalgia
Просмотров 119 месяцев назад
Chronic Heart 2 Heart Podcast Episode 6 Piper Interview Fibromyalgia
FX Make Up and Conversations Trypophobia Episode #22
Просмотров 119 месяцев назад
FX Make Up and Conversations Trypophobia Episode #22
FX Make Up and Conversations Deadite Make Up 2 Episode #21
Просмотров 29 месяцев назад
FX Make Up and Conversations Deadite Make Up 2 Episode #21
You Are Not Letting Others Down By Being Chronically Ill
Просмотров 1610 месяцев назад
You Are Not Letting Others Down By Being Chronically Ill
Chronic Heart 2 Heart Podcast Episode 5 Piper Interview Celiac Disease
Просмотров 1310 месяцев назад
Chronic Heart 2 Heart Podcast Episode 5 Piper Interview Celiac Disease
Chronic Heart 2 Heart Podcast Episode 4 David and HyperPOTS Part 2
Просмотров 1410 месяцев назад
Chronic Heart 2 Heart Podcast Episode 4 David and HyperPOTS Part 2
Answering Your Questions How Long Have I Had HyperPOTS
Просмотров 6810 месяцев назад
Answering Your Questions How Long Have I Had HyperPOTS
Chronic Dislocations/Rolling Dislocations With EDS
Просмотров 1110 месяцев назад
Chronic Dislocations/Rolling Dislocations With EDS
A Day In Life I am Sorry It Wont Happen
Просмотров 1911 месяцев назад
A Day In Life I am Sorry It Wont Happen
Chronic Heart 2 Heart Podcast Episode 3 Chris Interview HyperPOTS
Просмотров 3911 месяцев назад
Chronic Heart 2 Heart Podcast Episode 3 Chris Interview HyperPOTS
I will no longer give people the benefit of the doubt
Просмотров 2511 месяцев назад
I will no longer give people the benefit of the doubt
Lacking The Spoons Chronically Fatigued
Просмотров 2811 месяцев назад
Lacking The Spoons Chronically Fatigued
"May the force be with you"🙌💖😘
great
I too had thyroid cancer, at age 25..."the good kind"...and ha e not been the same since. Fast forward 20 years and now I have abnormal tilt table results and my lab work shows elevated norepinephrine and others. My primary care doc thinks EDS is likely (but not diagnosed) as well as Sjogrens (but not diagnosed). No focus where I am in WA (hard to believe they have all gone to cash only) so I am being sent to California. I feel so alone in all of this. I am also being sent for evaluation of a possible CSF Leak...the hits just keep coming.
I can smell the disappointment through my screen. Gtfo and find a real job.
Deus me livre 😮😮
It happens because healthcare is broken. No just in America but everywhere.
Hi, just stumbled onto your channel. I’m glad I did. I’m sorry you’re struggling. Advocating for yourself should not be so frustrating but I know that it is. 😢
It is for sure frustrating and exhausting at times. Welcome to my little corner of youtube. The struggle at times makes me feel alone but knowing that others feel similar helps me to keep going.
I know I'm not anyone from the medical system, but as someone who can relate to your experience in some ways, I just wanted to say that I see you and hear you. Thank you for saying the things that need to be said, and may you encounter the people that you need to see you and hear you most in a timely manner. Take care 🫂
This is very kind of you, thank you so much for this. I hope to be seen and heard and help others to be seen and heard along the way. Thank you for the kindness and the supportive words.
I feel guilty I haven’t came to your streams for this exact reason, but I’ve been pretty sick
Do not feel guilty this is about people making promises to hang out. I understand you are sick and appreciate what you do when you can. I am here for you! You matter, your health matters.
Thank Allah i dont have thee extreme condition with blood pressure and heart rate, mine normally go up when standing up or when i climb a stair, usually it gets normal within 2 to 4 minutes, but i have migranes, indigestion, chest pain for over an year now, and 2 months back i was having trouble breathing when walking, also had fatigue and loss of apatite. also 2 weeks ago was having trouble swallowing saliva, saw an ent doctor, he did a barium swallow x ray and said there is no issue. I have symptoms of heart faliure, throat, and lungs cancer. Last year saw a cardiologist and he did blood and treadmill test and everything was fine, he told me clearly he has no idea why its happening. He gave me Ciplar La 40mg. This medicine works, it controls tachycardia by 60 to 70 percent.
I am happy to do here that medication works for you. I am not sure if it is available where I am at. Have the doctors helped you get relief from the other symptoms you are having?
I have this too and am untreated. It usually is brought on by viral illness. Then will decrease in severity after a few months. I just got COVID and am dealing with severe symptoms. I have constant panic attacks, SOB, can’t sleep (sleep apnea now, I think), blurry/grainy vision, etc.
I am sorry to hear you are untreated. I am not sure why youtube did not notify me of your comment. I hope you have found some relief for your symptoms.
Have you lost a lot of weight?
@@juliaarambula3153 no. I am looking into EDS as a possible cause. I think eagle syndrome and TOS might be what I’m currently dealing with - which brought about the symptoms
😍 beautiful
Compression calf sleeves and saline infusions can help. The Alpha-2 agonists (Clonidine or Guanfacine) specifically target hyperadrenergic POTS by signaling the body to not dump so much norepinephrine and adrenaline into circulation. They've been wonderful for me. I have hypermobile Ehlers Danlos syndrome. I also have digestive motility issues, which have been eliminated by Mestinon (Pyridostigmine) - plus this medication can help a bit at mitigating POTS symptoms.
Nice video really helpt alot!
I am happy to hear this, your comment truly made my day!
As an introvert I hate my phone going off, it's permanently on silent, people hate me for not getting back to them quick enough, which bothers me but i also find things like that draining, glad to hear I'm not the only one!
I find it draining also. Responding when I can is what I do also. If it bothers others that is on them, I am introverted also. Having one’s space and peace of mind is important. I am glad we can relate on keeping the sounds off. 😊
🤗
My bp as of yet only spikes sometimes but spikes drastically. It can last minutes hours or days, but in between bp low 80s/60s so idl what can help me. I think a bp medicaton will make me bottom out. Its hard to live like this i can not evem go 5 min away from my house as a passenger in a car without spiking hypertensive 😢
Dr Dianna Driscoll has a great video she made years ago on this exact diagnosis. Highly recommend for anyone with this condition.
I have read the Driscoll theory. However, I didn't know there was a video do you have the link?
Dr. Diana Driscoll is who recommended Mestinon (Pyridostigmine) to treat POTS by stimulating the vagus nerve. She made an OTC supplement version of this medication, called Parasym Plus. I've had a lot of success on the Mestinon, although I primarily take it to treat my digestive motility issues.
You’ve met someone that has it, I have it
That you do and I hope that you are hanging in to the best of your abilities!
Because no one cares. People live their lives as long as they’re not affected, chronically ill people are ok as long as we are out of sight out of mind. On the flip side people will ask how you are just as a checkmark. Again I’m well aware you can’t expect others to be like I am and I can’t expect them to care. But it sucks nonetheless.
I think there are people that care and people can learn to care. For sure sucks to be ignored or forgotten but I have hope that there can be change.
Hi❤
Hello 👋
Were these symptoms all the time or just occasionally?
I wouldn’t say occasionally, it really depends on a lot of things. In a flare it can be often. I experience symptoms regularly but do what I can to cope with them as they arise.
Thank you for your videos. It is so hard to find information on HyperPOTS (and even harder to find a good doctor). I’ve been struggling for years.
Thanks for sharing and I’m so sorry for what you’re going through. I am going through some stuff at the moment and can relate to a lot of what you talked about ❤
I am sorry to hear you are also going through hardships also. I hope things improve for you. I appreciate the kindness. Glad we can relate it helps me heard and seen and understood.
Life is so unfair at times. Sending lots of love ❤️
It can be for sure, finding things I can still do has helped me a lot@@angelayoung8770
I get that. Dec is difficult for me as well. Lost my folks in the 90's, estranged from my sister and my friends are in BC. It's just me.
I am sorry to hear of the loss, it sounds like a tough situation. Thank you for sharing with me. Holidays can be hard when we are alone, but doing something for ourselves around this time of year I think is vital for showing ourselves self care. I game most of the holidays because I like my online community and I like gaming. I hope there is something you can do for you this holiday season, because you are worthy of good things.
@@Villainari_Oh yes, I have my rituals...junk food and some drinks Christmas eve and food on Christmas, and watching LotR's. :) I do have a game of Twilight Imperium set for New Years day.
i don't do anything for holidays because of celiac so being online is a new thing. i hope you like it and that it helps you enjoy this time of year.
I have spent many years online and do streams for Holidays because I know I am not the only one alone this time of year. I am glad you are online and that we met through the internet! I appreciate your friendship.
you're awesome @@Villainari_
This is always very interesting to listen to. Thank you for sharing your journey. Wishing you the very best for the future. <3
Thank you so much. Happy to share my journey of the things happening with rare and complex illnesses. I will continue to share. I wish you the best with the future also.
I thought Healthcare might be higher on the list
Healthcare in Canada means waiting 2-3 years to see a specialist, our healthcare is not what it appears to be.
Bloody lunatics
Get a life !
Are you mentally ill?
❤
Congratulations...epic🤘😈😈😈🖤
Thank you so much! Was fun to do!
Hope it went well!!!
Thank you hoping to do an update video now!
Oh I remembered exactly how mine began too 😅
Would love to interview you if you want to share your story, if not no pressure!
@@Villainari_ would be nice.
@@blevenzon will send you a message and we can set up a time?
@@Villainari_ sounds good
❤❤ you’re awesome
Wishing you the very best!!!
Sorry missed this, covid got the better of me ❤❤❤
Very good 😊
Thank you so much!
lookin forward to seein you soon. lots of love & support always
We have had a conversation or two...you can always reach out and chat! Be curious to hear an update on your project. Also, what you're going through is brutal. I consider myself lucky and I admire your strength! It's very commendable! #f*ukcancer
Awe thank you so much! I appreciate this greatly! My Documentary Project? Thank you for the kind words and the admiration. I agree cancer is a terrible thing and it should go away.
i help with cat pics =^.^=
thank you for talking about your experiences, fiona. big hugs.
I've been really feeling the appointment burnout this year-not only with my own appointments, but with others. All of us have some of the same chronic conditions that you do. I'm now trying very hard to strategize in hopes to prevent or at least lessen the effects. Hoping for all the best with your new doctor if that hasn't come to pass yet, and hope you get to do some makeup or video games before and after to hopefully cope with any possible re-traumatizing. Thanks for sharing, and take care 🫂
I hope everyone is able to take a week off of appointments if possible and if not hopefully have a few days without appointments. Thank you. I appreciate it. Happy to share. It is a thing that happens to many of us for sure.
@@Villainari_ Thank you so much. We have, thankfully, before some major ones each of us have coming up, and we're trying to keep them more spread out where possible. Of course! And definitely agree-I don't even hear many chronically ill/disabled content creators talk about appointment burnout, so I think I've come to the right place.
@@TheCloverAffiliate12 I hope you are able to do self care for you. I am happy to share my experiences as I have burnt out many times due to appointment burn out. Happy to have you here.
I also have fibromyalgia and I do exactly the same with my words. Also, I’m being diagnosed at the moment and you sound like me 🤗
I hope the diagnosis process helps you to find some resources and relief from symptoms. I get tongue tied so much LOL
@@Villainari_ I have to write a list of what I want to know otherwise I’ll forget 🤗
I do the same for all my appointments or I forget things@@carolharper268
🤗
Awesome as always
Awe thanks! I enjoyed doing this one, everyone made me laugh at the end LOL
Sorry had to drop early
No worries about that ever, I understand and appreciate you coming back when you have time. Never pressure to hang out in streams. It is always lovely to see you there, I support you in taking care of you!
I love how real and true you are! Loved this vlog!
Thank you so much!
thank youu!
Of course, it is always lovely to chat with you! I appreciate your kindness and your openness