Relationships and MS - Spouse or Partner Perspective 

What other questions do you have about being a spouse or partner of someone with MS or chronic illness?

A huge thank you goes out to both of you. Thank you to your husband so much for speaking it was great for my spouse to hear another man. It help to really open up the communication line in a deeper sense about MS. Your husband gets a gold star for his time, thank you. 🎉❤😊

I think both of you are such wonderful people and I love to see how health conscious and mindful you both are about your eating habits and how they affect your health. I also love your philosophy and how you approach life's challenges together and support each other so much. You both have a wonderful, positive attitude and I appreciate your both sharing.

What a beautiful video! Possibly the most uplifting video I've seen, and I've watched 100's since my PPMS diagnosis. Beautiful couple. Thank you both.

As a person who has begun dating someone with MS, your channel and this video have been very insightful. It's nice to know that many of my concerns are validated, but there's also an opportunity to live a normal and healthy life. Living on the present is much better than fretting for a future that has yet to happen. Communication is definitely key. So let's see how it goes. Thank you so much for the work you both do ❤

Aww you’re such a lovely couple - can feel the love and support! Thank you both x

Married 25 years been together over 30+ as well I think we also view things in the present. I also got diagnosed with a very large brain tumour which was found while looking for MS in 2021. Brqin surgery has progressed my MS alot. However I still support others with MS and run the MS Canada chapter near us. I find taking it each day at a time, because MS is always there, when I wake up till I go to bed. I knew I had MS way before I was diagnosed. Eachday brings new changes into our lives, some days better than others. I would say it has for sure made me think more about myself and what I need in my life. Meeting others with MS has been a blessing as well. Also found 1 or 2 others whom also had a brain tumour because of MS. It's very rare. I thank you both for being so open as i will share this video with my hubby. I strive to be that way as well, as it does come naturally often to me.

Thanks for sharing Steve 🎉

Great video. Thank you for sharing your husband.

Great video Vickie. Cheers to another 30 years.

I'm so happy you two have each other, and trying to stay in the present sounds wise. Thanksfor sharing this.

I love this! What a great way to hear from "the other side"🧡

Great Video. How did I not know your name was Vicky?!

Beautiful. You two are so lucky to have each other. My husband is in denial and just doesn't understand. It's always I'm fine I'm just lazy and nothing is wrong with me. He says he will never believe it because I look fine and I'm not physically disabled. 🥺 He does go to my neurologist with me and does see what the heat does to me. Do you have a video that could explain this for someone like that to better understand?

I also have MS and my husband went to Bates college I was a massage therapist before, and I help diagnose myself.

Hope you do a video on plant base food. I not a good cook and do not love vegetables. I need help and suggestions on how to cook vegetables

What kind of doctor diagnoses MS? I have been having some symptoms I have been wondering about.

Do you folks have children ? Since you never mentioned it I’m guessing no. Just curious.