@@ettakate35 thank you very much i used to feel I am the only one going through this but now I know that there are people like you that can help us going through this ,it gives me hope to keep fighting and don't give up, all the best to you 💗
Thank you for taking the time and having courage to share your stories. Your honesty is very much appreciated. I have a vestibular "something" as well and have been trying to cope with it for over a year. I don't have an official diagnosis because I have halted doctor visits and further testing for now. An ENT suspects vestibular migraines but VNG testing showed vertical nystagmus which could mean Central (Cerebellum) Vestibular disorder and loss of vestibular function in my left ear. It has been a very scary road to travel at times. I never knew I could fall into a darker pit than what I had been in previously in my life. But I feel I am healing, slowly but surely, and I am so grateful. I still have bad days but nothing compared to the REALLY bad days and my worst day which was right before a dream come true for me...seeing Justin Timberlake in concert. It's so crazy how my worst vestibular day morphed into one of my best days ever. The morning of the day of JT's concert I had the worst and first experience of vertigo which was the result of the worst migraine I had ever experienced. I was all alone in a hotel, afraid I'd have to cancel my dream and ask my mom to drive 3 hours to come get me. My life seemed to be ripping apart at the seams and I was spiraling into the darkest pit I never knew existed. Now here I am in 2020, looking back on that day and seeing how far I have come and still holding onto and pursuing other dreams despite not feeling like my usual healthy self. I still mourn the loss of incredible balance, vision, and health I used to have but I know that this journey is teaching me valuable lessons.
YES! It has helped us to slow down. Now I wouldn't change this journey, but a year ago I could not have said that. I used to joke that I would trade all this and become shallow again.
Thank you so much for posting this. I cried listening to your stories because I can relate to them all. I’m very new and was feeling so crazy and alone.
Awww I adore you gals & as most of you already know- I can certainly relate to each & every one of you in one way or another. Such beautiful words shared with those of us who GET IT & realize we're NOT alone! Thank you so much for being such great supporters of both myself & each other! HUGS HUGS HUGS to you all!! (JWalk JMMAWZ)
Vestibular Warrior keep these videos up. People are suffering through the world and can’t afford, financially, to get this info, so this is lifesaving.
This was so helpful. I’m a Vestibular Neuritis warrior to. I appreciate everything in my life. Eternally grateful. I feel as if my story is 💯similar to Etta’s . Re-evaluate everything in life. Thanks for sharing!
Etta Kate Hi Etta, yes I watched so many VN recovery stories during the dark trying times. I’m much better after 13 months. Thanks to all of you ladies.
This means so much. If you ever need to do this again, please message me. I have followed your approach as well. I'm now 90% better. I will never be the same ....
I'd love to slow down to heal....I'm really struggling very badly with symptoms right now and diagnosis is new as of January. Its thrown my world upside down. But....I have 3 kids, I have to work to support them. How. How . How. Do I heal and continue to work? I have been dragging myself there and back. My anxiety is through the roof and it feels like the weight of the world is on my shoulders. I HAVE to get better. Life is too short already, I feel like this is stealing time from me. I guess I wish I had the financial luxury to be more forgiving to myself. How do you guys deal with real "life"?
![ไข้ขึ้นเลย! เมื่อแฝดโดนจัดเต็มวัคซีนครบ2เดือน🤒 [cc] แดนแพทตี้ SS2 | EP.54 |](http://i.ytimg.com/vi/z2VHItnyyvY/mqdefault.jpg)
I cried watching Etta story, that is where I am right now, thank you for sharing and giving me hope that I am not alone
Hold onto that hope and know we are rooting for you!! Reach out if you need support. Sending good vibes your way💕
@@VestibularWarrior thank you for the kind words of encouragement 💕
I’m crying reading this! You are not alone, I promise. Em has a lot of great videos that are very informative and will give you even more hope.
@@ettakate35 thank you very much i used to feel I am the only one going through this but now I know that there are people like you that can help us going through this ,it gives me hope to keep fighting and don't give up, all the best to you 💗
🙏 Em this is brilliant - it means so much to be able to hear the others girls stories - there is hope - be strong everyone we will get through this ❤️
I’m so happy you enjoyed!! More to come 💕💕💕
Thank you for taking the time and having courage to share your stories. Your honesty is very much appreciated. I have a vestibular "something" as well and have been trying to cope with it for over a year. I don't have an official diagnosis because I have halted doctor visits and further testing for now. An ENT suspects vestibular migraines but VNG testing showed vertical nystagmus which could mean Central (Cerebellum) Vestibular disorder and loss of vestibular function in my left ear. It has been a very scary road to travel at times. I never knew I could fall into a darker pit than what I had been in previously in my life. But I feel I am healing, slowly but surely, and I am so grateful. I still have bad days but nothing compared to the REALLY bad days and my worst day which was right before a dream come true for me...seeing Justin Timberlake in concert. It's so crazy how my worst vestibular day morphed into one of my best days ever. The morning of the day of JT's concert I had the worst and first experience of vertigo which was the result of the worst migraine I had ever experienced. I was all alone in a hotel, afraid I'd have to cancel my dream and ask my mom to drive 3 hours to come get me. My life seemed to be ripping apart at the seams and I was spiraling into the darkest pit I never knew existed. Now here I am in 2020, looking back on that day and seeing how far I have come and still holding onto and pursuing other dreams despite not feeling like my usual healthy self. I still mourn the loss of incredible balance, vision, and health I used to have but I know that this journey is teaching me valuable lessons.
YES! It has helped us to slow down. Now I wouldn't change this journey, but a year ago I could not have said that. I used to joke that I would trade all this and become shallow again.
Thank you so much for posting this. I cried listening to your stories because I can relate to them all. I’m very new and was feeling so crazy and alone.
Awww I adore you gals & as most of you already know- I can certainly relate to each & every one of you in one way or another. Such beautiful words shared with those of us who GET IT & realize we're NOT alone! Thank you so much for being such great supporters of both myself & each other! HUGS HUGS HUGS to you all!!
(JWalk JMMAWZ)
Thank you Em
Thank you Ladies Blessings to you all 😍
This is outstanding! I first had symptoms 4 yrs ago. Several doctors, few diagnosis. I feel the same way.
So happy that you enjoyed it! More to come 💕💕💕
Vestibular Warrior keep these videos up. People are suffering through the world and can’t afford, financially, to get this info, so this is lifesaving.
This was so helpful. I’m a Vestibular Neuritis warrior to. I appreciate everything in my life. Eternally grateful. I feel as if my story is 💯similar to Etta’s . Re-evaluate everything in life. Thanks for sharing!
We hear you completely💜 I share other videos on this channel about healing VN that I hope you find helpful. Rooting for you on your healing journey!
Thank you so much for your kind comment. Em has some really good videos about VN that helped me through some very dark times.
Etta Kate Hi Etta, yes I watched so many VN recovery stories during the dark trying times. I’m much better after 13 months. Thanks to all of you ladies.
thank you!
This means so much. If you ever need to do this again, please message me. I have followed your approach as well. I'm now 90% better. I will never be the same ....
More please
Coming soon
I'd love to slow down to heal....I'm really struggling very badly with symptoms right now and diagnosis is new as of January. Its thrown my world upside down. But....I have 3 kids, I have to work to support them. How. How . How. Do I heal and continue to work? I have been dragging myself there and back. My anxiety is through the roof and it feels like the weight of the world is on my shoulders. I HAVE to get better.
Life is too short already, I feel like this is stealing time from me. I guess I wish I had the financial luxury to be more forgiving to myself. How do you guys deal with real "life"?
We hear you. We are taking about this soon.
Ladies I Love you I feel your pain Please God help us.
Thank you. I'm in the dark right now. Trying to figure out how to continue working. I have to work. Meds arent working yet. I need hope.
What is ettas email?