Multiple Sclerosis 10 Year Anniversary | Tips and Tricks, Symptoms Relationships and How To Cope
Вставка
- Опубліковано 3 жов 2024
- Hello my loves,
It is officially my 10 year Anniversary with Multiple Sclerosis. I am shocked at how quickly the time has passed. It has been such a journey and I have learnt so much along the way. All of what I share from my medication to managing my symptoms and the various tips, tricks, supplements and herbs, are things that I do every single day to help me live a happy, healthy life.
I have also learnt over the years that paying attention to yourself on a holistic level - mind, body and soul. Makes the world of difference in how you cope with your Multiple Sclerosis.
By nurturing all parts of myself, I am able to really move forward and beyond my diagnosis. Of course, not ignoring the very real reality of having a disease, but finding ways to heal so that I am not bound by it.
I share a little bit about my diagnosis, symptoms, medication and how all of this has shifted over the years. Overall this video is extremely positive and my hope is that you can take something from it to incorporate into your own life.
Find me:
IG: @becca.is.love
Podcast: Ceremony of Love
Music: Epidemic Sound
You’re so cheerful even with having MS. You give me so much hope. There’s a possibility that I have MS. I’ll be seeing a neurologist soon and have a spinal tap done. I had a MRI done and spots in my brain showed that there a possibility that I have MS.
Good luck! I know it’s scary but the sooner you know then the sooner you can be put on a treatment plan that works for you ❤️
Excellent re: stress. And boundaries. I was horrible with it, as I felt as a sensitive empath (with ptsd from childhood issues, where most autoimmune diseases originate actually), so bad. Boundaries was a "bad word' to my family...toxic traits are just as bad as mold or other physical triggers. So important to go there. All excellent items. I pray you much success here as you help others, which when we do so, it affirms ourselves, too, right? WIN WIN, Not woo woo :) Ciao for Now, thanks again!
So true! We really do need to pay attention to boundaries and toxic relationships as much as the other stuff ❤️❤️ thank you so much xx
This video really helps with this new life, i was just diagnosed the 14th with MS
and its still pretty heavy and i havent fully processed this “new-me” but i greatly appreciate all of your tips, thoughts, and insights on cooping with the episodes
Oh gosh, it’s really tough in the beginning❤️ just make sure you’re taking time to process but also knowing that it’s okay if you still feel emotional about it as the years go on. Good luck xx
Thanks for the tips and info.I was recently diagnosed a couple years ago though I was having symptoms for years but I never went to the doctor then about a year before I got diagnosed my balance and ability to walk got really bad not to mention the chronic fatigue and spasms. It took about a year before they finally had me do some MRIs and they found some lesions on my brain and spine. Now my Neurologist has me on infusion therapy for about a year now,so things aren't too bad just trying to adjust and stay positive. Thanks again for the tips!
It is quite an adjustment but at least you got a diagnosis and can now go on a treatment plan that works for you ❤️ good luck
Amazing to hear you share! I love your videos
Thank you so much 🥹❤️
💎❤️Wendy
Just take care re: chamomile, as it reduced progesterone level which we as women need, big time!!!!
Oh wow, I didn’t know that. Yikes! Thank you for sharing
I'm so sorry, dear. I'm riddled with "stuff" stuff, just wondering though...did you ever get a test for EBV, Mold or were you recently vaccinated with shots, or were you ever on birth control? I will pray for you, please pray for me. Have you used HBOT or IV ozone? I'm so glad you are improved with quality of life. The fatigue/neurological are the hardest for sure!
I’ve never had the EBV and haven’t been tested for mold - but would probably come up positive for mold because I’ve spent lots of my life in moldy homes🥲 I think the mold also contributes to the fatigue and brain fog (but like I said I haven’t been formally tested it’s just a hunch).
Will definitely keep you in my thoughts. Sending all my love ❤️❤️🌸