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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.

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.

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.

❤❤❤

This is really good content

👍🏾Respect Ladies

I have to say BIG UP!!! to you guys

😇🙏💕

Well done for sharing your experiences...

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.