You Get What You Give

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  • Опубліковано 25 сер 2024
  • This week, Christina and Jamie discuss feeling trapped, missing high heels, their favorite shows that they’ve worked on, and more.
    This episode was recorded in early 2024.
    This episode is sponsored by:
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КОМЕНТАРІ • 16

  • @Jackie-hp8xh
    @Jackie-hp8xh Місяць тому

    I love listening I call myself a Christiana your lucky to have a Jamie and enjoy the honesty &being real love you both

  • @annagrisham2215
    @annagrisham2215 Місяць тому +1

    I cannot imagine being in Christina's position. She honestly can't leave the house without being photographed. And the tabloids are so cruel. I feel like that has to be a factor the rest of us never have to deal with. I gained 90 pounds before I found ny third neurologist. I didn't want my picture taken. LOVED Jamie in Big Sky. If I'm honest, she's the reason that I kept watching the show. Dead to Me was a bold and brave role that made me laugh and cry.

  • @nancyt.8799
    @nancyt.8799 2 місяці тому +1

    I LOVE your honestly Christina! ❤ Let it all out. Suppressing what you really feel makes our disease symptoms even worse. Sometimes I don't want to push through the pain...and I don't feel like being a "hero" or a "warrior" all the time. My superhero cape sometimes has holes in it.

  • @austinsgro
    @austinsgro 2 місяці тому +1

    It has been less than a year since diagnosis in January, which took about a year to have a neurologist listen. Yeah, i see Jamie's side of it, but i am in Christina's head space right now. Truly feel spend everyday and I don't truly have anyone that understand. The point where being depressed, crazy because i just told my other half i feel like im in darkness. I sent you guys a long email when i first heard this podcast. Hopefully, we get to conversate at some point. Much love, i try to have my other half listen she feels like because 10 years old, she feels more pain looking for a group here in Tampa,Fl hearing you guys makes me cry and feel better. Light will come.

  • @jodirobinette1874
    @jodirobinette1874 2 місяці тому +2

    Hi Christina, all my childhood/teen years I was told we were twins, looked a lot alike and, by the way we are the same age. I have a brain tumor, spinal tumor, bladder disease, TMJ dysfunction, BPD traits, Grovers disease and going blind from a medication I took for 7 years. Yep, fuckin pissed off at the world. What changed my pissed off ass was listening to NDE, near death experiences. It shed light on why we are here, what we wrote and why we wrote our live experiences before coming to Earth for another life journey...just an idea to help you.

  • @JoetteDolce
    @JoetteDolce 2 місяці тому +1

    Aw Christina I think your beautiful wonderful and your story and all your honesty about your life I'm truly sorry for you to go through all this 🙏 big hugs from Canada

  • @JoetteDolce
    @JoetteDolce 2 місяці тому +1

    She's in a funk and it's understandable love you Christina

  • @michelletodd4893
    @michelletodd4893 11 днів тому

    I've had this monster 17 years. I know where Christina is at and it will get better. Listen Jamie-Lynn. Okay after 40 neurologist is not necessary. We no their is no correlation between lesions and disability. You can have 40 and be at a 2 on the disability chart, none and be completely disabled. Gut. Remember your "motility" is changing. I push my blind, ms, can have another heart attack due to oxygen problems. I did physical therapy and now I do serious house keeping. And walking when you are legally blind and drunk walking is a work out. I don't trust doctors because I was guinea "pigged" 2 x and didn't realize. When I was diagnosed they did steroids. But I said I don't have cancer, I don't want chemo that may give me cancer. Throwing this out their. Screw the mylen. It's the inflammation that is doing the damage. The tries to make new bath ways, but if there us inflammation in the body part, it's tearing it down. I think that's where research needs to be. One day MS will stand for Mystery Solved. My aunt had it. She passed 10 years ago. Her last 10 years was bed bound unable to do anything. I don't want that. And she was like you and Christina, she had the money to get best care and also in Europe so health care free or you can pay for better. Just keep pushing. I have my 14 year old who has always had a sick mom and my 28 year old who had corporate climbing mom till she was 14. I was in hospital month ago for GI bleed. I have achalasia - fun autoimmune not related to MS. We'll if course the do echo cause if heart, looks good, neurologist and gi. Everything good but neurologist. Dud quick scan and showed chronic shrinking and the lines are deeper. But I don't feel different. Thanks for letting me ramble. I think at the 15 mark point we all go f. It. I got MS and I understand what that means. But I will push myself till I can't. I won't complain. I will accept every new disability and learn how to live with it. I hope Christina gets her butt in gear. Think that happens year 3. Because she is more than MS.

  • @SuzyG-ij1vk
    @SuzyG-ij1vk 2 місяці тому +2

    Try Vionic shoes. Sometimes have very cute sandals that have great arch support and stay on your feet while walking. Comfy and some sparkly options. Cannot wear heals due to a neuro disorder that caused me progressive asymmetrical peripheral neuropathy and balance issues for the past 19 years. Was very upset about the inability to wear heels. Couldn’t bring myself to wearing ugly orthopedic shoes. Found this brand. Each year they have a sandal, flip flop or boot that I buy.

  • @patphatkitten
    @patphatkitten 2 місяці тому +1

    Christina, your MS is curable. You need raw saturated fats and raw unsaturated fats.
    Look into Aajonus Vonderplanitz,
    Carnivore diet, Ms. Budwigs raw cottage cheese and raw flaxseed oil mixture.

  • @MK-fi6mh
    @MK-fi6mh 2 місяці тому

    Ms. Applegate I’m sorry but your negative view points made me upset lot of great humans live with MS without being depressed - sorry I can’t

    • @lesleymichelle8250
      @lesleymichelle8250 2 місяці тому +1

      If you’ve met one person with MS, you’ve met ONE person with MS. No 2 people with MS have the same symptom set. Depression is very common with this disease. Trust me. I cry almost everyday. You don’t get to shame someone for having “negative view points”. You don’t live in their head. When I heard Christina’s words, I bawled. I could’ve said those words myself. Too many people sugar coat having MS or keep it hidden altogether. Right now, depression is where Christina lives. And that’s okay. She’s certainly helping ME 30:46 by being raw and honest. I can SO relate. It’s hard, for me, to be “positive” about MS after all it’s taken away from me. I grieve everyday. The loss of independence, not being able to drive, having to use a cane, giving up my past job as a radio announcer, vision loss, weight gain because I have too much fatigue to move, depression, not leaving my house for fear of bowel or bladder incontinance, slurred speech, loss of friends because of pushing them away and they just give up, and on and on. Trust me!! Negativity happens. A lot. And it’s a hard shell to smash.

  • @MK-fi6mh
    @MK-fi6mh 2 місяці тому

    Stop being sooo negitive