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Motivated Souls
เข้าร่วมเมื่อ 23 พ.ย. 2020
This channel was created to cover black and minority ethnic men and women's experiences with Multiple Sclerosis in the UK. Being a black woman or a man of any ethnicity with MS is not common. We plan to show the life of MS and the different things that affect us and our brothers and sisters. But most of all to show it is NOT THE END.
Please watch, leave comments and subscribe
Thanks
Misha, Amber and Miriam x
Please watch, leave comments and subscribe
Thanks
Misha, Amber and Miriam x
Relationships Pt 2
Continuing the conversation of relationships, further points of friendships, relationships with family, and any other relationships that we may encounter. Tell us bout your relationships that you may have and do they understand your MS???
Don't forget to Like, Comment and subscribe 😘😘😘
Don't forget to Like, Comment and subscribe 😘😘😘
มุมมอง: 48
วีดีโอ
Relationships pt 1
มุมมอง 213 ปีที่แล้ว
It's been a longggggg time.....apologies......schedules. children etc..... Just to explain in summary we have changed the name to Motivated. Souls (A. play on words of MS) Hope this doesn't confuse anybody! We want to still put out good content, talk about MS within the ethnic minority communities. So please Like Comment and Subscribe 😘😘😘
MS and PARENTING Pt 2
มุมมอง 353 ปีที่แล้ว
We are just carrying on the convo of the trials and tribulations of being a. parent with MS or a chronic illness. Like, Share, Comment and Subscribe ❤️❤️
MS and PARENTING PART 1
มุมมอง 393 ปีที่แล้ว
Parenting is difficult enough regardless of having to deal with MS. Amber Miriam and Misha discuss the trials and tribulations of parenting. The girls talk about how they deal with their kids, ages and overall stress and joy of parenting.
MS AND PREGNANCY
มุมมอง 723 ปีที่แล้ว
Research has shown that Pregnancy can eradicate symptoms of MS for 9 months, with one big relapse after the baby is born. Amber Miriam and Misha share their experiences as all have children with different experiences. Share, Like and Please Comment on your experiences maybe be different it will be. interesting to hear.
MENTAL HEALTH in COVID 19
มุมมอง 433 ปีที่แล้ว
This was just a short discussion on not particularly MS but essentially being disabled in current circumstances. Also the issue of the lockdown. At present we have been locked down 3 times. What has this done to your mental health? How are you coping? Like, Comment, and Share X
JUST HAVING A CHAT
มุมมอง 523 ปีที่แล้ว
Initially, we had an idea of what we were going to talk about. In the end, it ended up just having a chat!!!! This is an insight into what a phone call would be between Misha, Miriam and Amber!
DISCUSSING DIFFERENT TYPES OF MS WE HAVE AND ITS EFFECTS
มุมมอง 1713 ปีที่แล้ว
In this video, we discuss the different types of MS we have. Miriam and Amber have Relapse remitting however, this takes many different forms through each person. Misha has Primary. Progressive which is very different, Watch, like, share and comment tell us your views. We would love to know if the content is good for viewers.
PERSONAL TRAINING and MS
มุมมอง 783 ปีที่แล้ว
Misha and Amber have a very small discussion about personal training and the different hurdles that they have in training people with MS. Details of the different trainers; Ambers trainer -Andrea Allen - contact on Facebook Misha Trainer - @chisolifts on Instagram, Twitter, Facebook
EXERCISE WITH MISHA , AMBER AND MIRIAM
มุมมอง 723 ปีที่แล้ว
In the following video; Misha exercises with @bodybyCiara on Instagram she includes; dynamic exercises (squats, lunges, jumping) all that she uses the bannister to stabilise her. Miriam does mainly core exercises and floor work. Amber does a mixture of Core, Coordination and some Dynamic exercise. Try some of them Comment if you have any that you feel we've missed Move ya body.....Happy Exercising
MORNING ROUTINE’S
มุมมอง 953 ปีที่แล้ว
This video is a small clip of what Misha and Amber do every morning with MS . This video only includes Misha and Amber as Miriam couldn’t make the video . Make sure to Like, Subscribe and turn on the notification bell. The links for MIRIAM, MISHA and AMBER’s STORY: th-cam.com/video/rpVpDaqDOC8/w-d-xo.html -MISHA th-cam.com/video/zLALtBsZUug/w-d-xo.html -AMBER th-cam.com/video/_GNCFx9ymdI/w-d-xo...
MISHA’S STORY
มุมมอง 2163 ปีที่แล้ว
This video is about MISHA’S STORY with Miriam and Amber. Make sure to Like,Subscribe also turn on the notification bell. The links for MIRAM’S STORY and AMBER’S STORY are here: AMBER’S STORY: th-cam.com/video/zLALtBsZUug/w-d-xo.html MIRIAM’S STORY: th-cam.com/video/_GNCFx9ymdI/w-d-xo.html
AMBER’S STORY
มุมมอง 3043 ปีที่แล้ว
This video is about AMBER’S STORY with Misha and Miriam. Make sure to Like, Subscribe also turn on the notification bell. - The MS Bame Experience
MIRIAM'S STORY
มุมมอง 3693 ปีที่แล้ว
This video is about MIRIAM'S STORY with Misha and Amber. Make sure to Like, Subscribe also turn on the notification bell.-The MS Bame Experience.
Great podcast, wish you guys the best. Godspeed 🫡
Just found your channel through Twitter, I spent two years in England (I loved it there) when I was stationed there while serving in the USAF had to get out because of my health in 2008. I blew out my back, had major back surgery by 25yrs old 2006, Cancer Survivor 2011, mini stroke 6 months after that surgery. Had 3 seizures 2014-2015, thought nothing of it. 2016 MRI showed a spot in my brain stem. ER's and eye drs acknowledge my MS, but VA does not, though they denied my cancer and had I not been homeless to rcv state insurance I wouldn't be making this comment now. Now, I have to get an injection in my left eye every month because it bleeds, I could lose the eye, hoping not. I have experienced the MS Hug. And I have extreme vitamin d deficiency, now that you mentioned it, I need to go get it and restart taking it again. I think women in general are in denial. I don't go to the Dr for it, because I don't want the meds, I want to do this naturally. So yoga, meditating, stretches, breathing exercises, I eat like crap so that needs to change. And at first, long ago, it was RRMS, but I think I've progressed. Please keep making real life videos, y'all are awesome!
Thank you for sharing your experiences, it is really good to hear your frank accounts of pregnancy and childbirth while also living with MS.
Wow! Well done for sharing your story. ‘Raving hard’ 😂
Great discussion, Thank you. In summary, what would be your 3 top tips be on reflection to ensure a positive experience: Re: Ms and being pregnant? I.e ensuring good support etc was one that was highlighted.
Thank You for your question, in terms of support we mean; If it is a partner, friend, parent, in-law etc. It's just someone that can help with the feeding, the changing, all things that come with it a newborn. Having a baby and also having a disability is tough, so support is fundamental.
I liked this. I have been trying to research for a vid like yours that informs everything in this TH-cam video! 🧑🏻⚕️Your breakdown really is like the vids from Dr. Ethan! Doctor's demonstrations are actually insightful and I actually learned a lot for diet. He is the helpful Doctor in Nottingham and he talks about health and vitamins. I suggest you watch his YT out and give the Doctor a like here! ➡️ #DoctorEthanOnTH-cam
Hey ladies, don't say my MS or your MS, don't own it.
That’s a very good point......Thank you
I hv MS but MS doesn't have me
Keep up the battle Amber ❤️ you’ve done amazing and I’m sure all you do with your group and this page will be of great support to others and a great out let for you.
Naomi❤️❤️ it’s all love, this platform is just rite for ppl who have ms and feel alone. I dnt want anyone to feel alone 🙏🏾
❤❤❤
This is really good content
👍🏾Respect Ladies
I have to say BIG UP!!! to you guys
😇🙏💕
Well done for sharing your experiences...
Thanks it’s more for people to know that are not alone
I have watched all 3 posts: Well done-SO Inspiring and useful for others. What would you suggest in the way of advice for those that might be experiencing symptoms and are in denial? A useful point was made Re: In particular the black community who may ignore or deny signs and symptoms until its too late? Thanks so much for an excellent and brave post. STAY STRONG.
Thank u xx just trying to show that ppl a lot alone with this illness
Thanks for the comment. Statistics show that the majority of black people that have been diagnosed with MS tend to ignore, and are in denial. So the answer to the question is YES. But the three of us are intending to stay strong in order to show MS hasn't got us we have MS