Multiple Sclerosis Treatment VLOG | Ocrevus Infusion
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- Опубліковано 23 тра 2024
- Hello my loves,
I decided to vlog my ocrevus infusion, because I think it will be super helpful for anyone undergoing MS treatment via infusions (even if it isn't ocrevus). Overall, I had a really great experience in the hospital. I share some tips about how to make your own infusion process go smoothly - what to pack in your bag, how to prep your body and self care post infusion.
Everyone is different and so find what works for you and stick to it. Be extra gentle with yourself and support your mind, body and soul.
IG: @becca.is.love
Podcast: Ceremony of Love
Music: Epidemic Sound
![3 Natural Home Remedies [MULTIPLE SCLEROSIS CURE?] MD Specialist Explains](/img/n.gif)
Well done and continue the good works
Thank you so much ❤️❤️
The chill vibe of this is just what I needed before I have my rituximab infusion for RRMS. Thanks for sharing your infusion day! I'm going to try to get out in nature tomorrow after I have my infusion. ❤
Please do ❤️❤️ best of luck 🌸🦋🦋
Hi 👋🏽
I just wanted say that you are really great and amazing for having a strong sense of self care and that your videos really are a breath of fresh air. I'm glade your treatment went better and I hope that you enjoy the rest of your day❤. Oh, I did want to ask, are your treatments monthly or do you receive them every 6 months?
Wow! What a kind comment❤️ thank you so so much
My treatments are every 6 months so just twice a year! But I know some MS treatments are monthly xx
@@rebeccashain good to know, thank you 😊 Again, I love the videos you make! Please keep going and making at you own speed, because they do help 🙏🏽💎
@@magicelfyonanisle3354 that makes me so happy ❤️ I really want to continue making videos. So glad to know they help xx
Hi Rebecca. You might want to consider stem cell therapy. Mesenchymal stem cell therapy. I could give you the contact of a trusted clinic.
It’s not something I’m interested in right now 💖
I sympathize with you about forgetting that we have MS until the bad days hits. I forgot how tired I was from MS until I stopped the medical drug copaxone due to a dangerous side effect of that drug. So now I am without the medical drug until they approve my new medical drug tekfider. Good luck to me.I wish you to feel good with MS and happy.😊
Thank you so much ❤️ I’m so sorry to hear about your tiredness. It’s such a tough symptom and I totally relate. Good luck with your new treatment xx
@@rebeccashain ☺💖