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I love your podcast and have been a subscriber since day one. Particularly the episode with Katie Couric. But Christina, you’ve never heard of Kamala Harris? For real??
Can you guys talk about what medication you are on at some point or that’s not allowed.
so awesome. i love that you two say how it is. MS sucks.
They have been checking me for MS for 5 years. I walk with a walker, and my voice slurrs a little. I have had 7 MRIs with 1 lesion. My daddy had MS.
My husband is definitely embarrassed of me when we go out.
AND SO IT IS AND IT IS SO LUVIT THANK YOU THANK YOU THANK YOU BOTH FOR ALL U GUIRLS SHARE APPRECIATE BIGTIME🙏❣️🔥💞💝
right on about bringing diapers to the forefront! i can relate 😆
Thanks for flowin!! You guys are amazing. Thank you for sharing your lives and experiences.
Love love love sooo gr8ful appreciate all u guys share & SO IT IS AND IT IS SOO THANK YOU THANK YOU THANK YOU 🙏❣️
Your podcast is reminding me of how much I love you Christina. I just want to get the message to you.
Love you both and LOVE this podcast! Thank you for your quick-witted, raw, tell-it-like-it-is honesty, Christina!!!
You guys are awesome. Thank you so much for oversharing. I don’t even tell these things to my husband! I hide everything from everyone!
I think it’s great that you’re talking about the diapers and all these other topics. I was diagnosed in 1998 with M. S and have been hiding and not discussing any of these things. I really appreciate you two! Thank you!
Zinger folds like a folding chair. It’s so compact. It fits in the back of my mini cooper. And it’s fun to drive and goes really fast. Please check it out on YouTube.
UUUUGGGHHH cut me off intravenous steroids prednisone and completely did major life changes definitely went through it still going through it but hey aren’t we all luv all u girls did n do thxxx bunches
And Miss Christina I also experienced eyes going bonkerz relapse admitted into hospital cracra had no control of my body especially eyes could not focus and stop them from moving back and forth on their own own was horrible was put o. In tobeniois
Love your podcast. I have a bad knee and use a cane. I use walls and furniture in my house to get around. My issue is arthritis and constant pain. Don’t want to go out. Sending hugs.
You guys are awesome, thank you for not sugar coating this awful neurological disease.
This is great! I enjoy listening to the conversation between you all.
When people would ask my dad how he was doing, he would answer, ”No better, no worst
Thank you for your honesty. Love ❤️ you both! This is my favorite Podcast!
I can’t express my gratitude for this podcast. I was diagnosed with breast cancer and brca2 in 2022. Now, still dealing with that aftermath- I have been diagnosed with chronic fatigue, and possibly lupus (I start seeing rheumatologist next week). Thank you 🙏❤️
You kids are killing it! Although I don’t have the MS thing, I have an ostomy thing and an ism thing. And really, it’s all the same thing. Thank you for sharing! Andrew
Hello! Stefan from Sweden here. Just wanted to say that I really like the first episodes, and now I’m looking forward to the next ones. Believe me, I share your pain, worries and everyday challenges caused by this disease, but simply by talking about it on your MeSsy podcast, you tell MS-people everywhere they’re not alone in this. And sharing is, kind of, caring. I, at least, support you wholeheartedly. I was diagnosed with primary progressive multiple sclerosis on May 28th 2021.
Wow this is so amazing! I have had MS for 9 years, diagnosed at 31 and now walk with a walker. MS sucks but it’s nice to listen, laugh and cry with people who truly understand.
Love you both and podcast. look forward to more. I too, have MS
so happy to have this podcast. spreading the word about MS is so important because this invisible disease is so hard to explain to people, because it is so individually based. thank you.
Good show.