MS Stories - Why We Create MS Content
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- Опубликовано: 4 ноя 2023
- Why do we create content about living with Multiple Sclerosis (MS)? Why do we share “My MS Story” videos? I decided to share my MS story in 2019 on RUclips . In this video I share why I decided to start my channel and my thoughts on why it is important that we share our stories on RUclips, in blogs, on podcasts, and in newsletters. I also share how it can be challenging at times and how it can be rewarding too!
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• MS Stories - Why We Cr...
*Stay in touch!*
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*15 Simply Nutritious Plant-Based Meal Plans eBook*
Need inspiration for plant-based meal plans to get you in and out of the kitchen fast? Order my eBook here sowl.co/s/Rc5Fh
*Check out my Amazon Storefront for other stuff I use to help me live well with MS* (As an Amazon associate I earn from qualifying purchases.) www.amazon.com/shop/evensoiti...
*Links to Blogs*
acoupletakesonms.com/
ahotms.com/blog
trippingonair.com/
*Photos*
Anna Spafford By Bertha Spafford Vester - "Our Jerusalem" Published in Lebanon, Public Domain, commons.wikimedia.org/w/index...
Horatio Spafford By Unknown author - Unknown source, Public Domain, commons.wikimedia.org/w/index...
The information on this channel is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. It is for educational purposes only. Always consult your doctor for professional medical advice.
#MS #MultipleSclerosis #LivingWithMS #EvenSoItIsWell, #VickieHadge
![Neuro - Multiple Sclerosis & ALS [Recorded LIVE!]](http://i.ytimg.com/vi/EZs1sN4u6Lo/mqdefault.jpg)
![Neuro - Multiple Sclerosis & ALS [Recorded LIVE!]](/img/tr.png)
Leave me a note in the comments! I want to get to know you my dear friends!
Great to see so many people creating content and helping people! 🙂
Right?!? I have found so many helpful content creators.
Thank you so much for all your videos! Helpful, empowering, and motivating every time. Your channel helped me to believe that I can do this! I can have a great life with MS. Thank you❤
Thanks so much! I am so glad you are finding them helpful. And yes, you can do this!!
Thanks for all you do. I am inspired to do something similar for POTS folks. I hope I can aspire to your level of grace and giving. Keep up the great work. I don't have MS but I have something "undefined" as of yet with MS features. It helps to compare stories and it always helps to have positive / proactive role models.
Good on you Stephanie! Definitely let me know if you start something and how I can support you!
If you put yourself on social media, you are fair game for darts and/or roses. Darts teach you to be open minded, respectful, and compassionate of others ideas. The roses help to lessen the dart stings and sometimes teach you new ideas and perspectives. As long as you are happy in the limelight and it’s not a stress, you are winning❤
Thanks so much Myrna! You are so right. 💕
I love that necklace with your sweater. Your videos are inspirational too.
Thank you for both!
Good to hear and it's a question I often think about ... so many motivating factors!
Thanks Spencer! Your channel was one of my inspirations!
@@EvenSoItIsWell it's cool to see how yours has developed over the years :)
Thank you Vicky for all videos that you do. You provide so much valuable information! Every Sunday morning i find myself looking for your latest video. The recent video regarding vitamin B12 deficiency is one that i found particularly interesting and very helpful. They are wonderfully presented! X 😊
Thanks so much David! I am glad you find them helpful!
I’m new to the community, 7/23… I appreciate your videos so informative
Welcome Francesca! I am glad you are here! Newly diagnosed as well?
You have a lot of fans who really appreciate your hard work and helpful content. I’m definitely one of them. In a guided meditation I listen to they say, “Negativity is a form of suffering and should be met with compassion.” Thanks for all you do.
“Negativity is a form of suffering and should be met with compassion.” I love this!! Thanks for sharing and thanks for being a fan!
There is obviously so much work involved in producing each of your videos because you do share science back information. All the time and energy that you spend creating. This content is greatly appreciated. Your newsletter is just as beautifully produced as your videos. Thank you for all you do.
Thanks so much Ann!
Heartfelt thanks for your videos. Keep them coming. Your hard work, extensive research, passion and sincerity make your videos a go to for me. Even after 33 plus years with MS, there is always something to learn or revisit.
Thanks so much Marc!! I appreciated that and you! It is really amazing how much we can learn and how much is changing isn’t it?
I've been trying to learn about MS's impact on the vagus nerve. Seems like there can be an impact on autonomic functioning. There is a direct pathway to and from the gut and the brain stem. Maybe that's why someone has neurological systems when eating poorly. (The vagus nerve is mylenated and long. Not sure if part of it can be viewed by an MRI. Lower part perhaps by sonogram or xray. Will be researching. Maybe you know something on the topic. If do, please share.
Thanks Marc! I have been interested in the vagus nerve and how it functions but I have not done a deep dive on it yet. I absolutely agree that the gut brain connection is huge! The gut has been called the second brain. Check out my videos on the Microbiome ruclips.net/video/exxe4jL-HxI/видео.html
ruclips.net/video/P4dQFRrLLxk/видео.html
@@EvenSoItIsWell will do! Tx
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Thanks for watching and commenting! 💕
Thank you so much for your hard work. I never got into the MRI beast.😢 I'll just leave it diagnosis unknown. Put it in the old age . I stay on a good diet and do work projects . The weird system oh well.😢
Thanks for watching Nancy! I hope you continue to do we with your self care.
I don't think I could handle all the comments, can't handle my families comments. I've had to change Dr's to, medical for ms sucks, first neurologist said I wasn't bad enough for mris. I feel I have ms too and my family thinks I'm making it up no one wants ms but I have two cousins w it. I love seb.
Thanks for watching. Yeah, the comments can be hard sometimes but most of the comments are awesome!
I am sorry you are struggling with doctors. Keep advocating for yourself and seeking answers. It can take some time with autoimmune diseases.
I love Seb too!
Thank you, you make my day I have Ppms
Thanks so much for watching and being part our community!! 💕
Some of these "haters" I wish they could get a chronic illness, it's madness having symptoms seeing a doctor then playing with your life as if it's a game of clue to figure out what is it and can we treat it or manage it. It would be like people telling me bipolar disorder is all in my head. WHERE ELSE WOULD IT BE?
I also live with MS I wanted it to be a pinche nerve so badly. Turns out it's BOTH MS AND the pinch nerve. I was diagnosis 2013 I accepted it was MS in 2020.
Thanks Minnie! Dang! MS and a pinched nerve? That is not fair or good.
The tingle feeling are symptoms of both. luckily the pinch nerve stops when I stop the activity that triggered it as long as a flare up of MS is not happening at the same time@@EvenSoItIsWell