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. ❤
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?
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.😊
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 🌸🦋🦋
Well done and continue the good works
Thank you so much ❤️❤️
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 ☺💖