I was on Plegridy (a bi weekly interferon injection) for six months, but I suffered quite badly from the flu like side effects of the interferons. It put me in a really bad head space, and gave me anxiety. I had to stop because my white blood cell count was dropping too low, and my Dr wanted me to stop to let my levels go back up, and while I was off it I realized how badly it was affecting me mentally and decided not to go back on it.
I have been watching you and its so helpful i was happy yo know every thing about mavenclad and you finshed your second year my question any improvement in your condition?
Hello dear, me and you are quite similar, also got diagnosed in 2017, started with Pledigry (which did not work), so I tried Mavenclad for 2 years. Dunno yet weather I might start the 3rd or not. I have a question for you.... During the 2 years of Mavenclad, have you experienced any relapse of the MS, even mild, such as trembling fingers or transient drop of monolateral eyesight? Cause I have.... and I don't know if it's normal or not.
Thank you for sharing your story, please post an another update, Hope all is well.
So happy for you. All the best.
Pls keep doing these videos 😊
So glad you updated as I am nervous to hear that you will not be on a treatment. Good to see you! Any symptoms still ?
No side effects from Mavenclad. And no new lingering MS symptoms.
Were you on a different medication before Mavenclad? I have been on Rebif since 2016 and the needles are getting to me. I want to be done with them
I was on Plegridy (a bi weekly interferon injection) for six months, but I suffered quite badly from the flu like side effects of the interferons. It put me in a really bad head space, and gave me anxiety. I had to stop because my white blood cell count was dropping too low, and my Dr wanted me to stop to let my levels go back up, and while I was off it I realized how badly it was affecting me mentally and decided not to go back on it.
I have been watching you and its so helpful i was happy yo know every thing about mavenclad and you finshed your second year my question any improvement in your condition?
No improvement, but my condition is very mild. No improvement, no worsening, so I’m very happy.
Thank you for updating😊
Hello dear, me and you are quite similar, also got diagnosed in 2017, started with Pledigry (which did not work), so I tried Mavenclad for 2 years. Dunno yet weather I might start the 3rd or not. I have a question for you.... During the 2 years of Mavenclad, have you experienced any relapse of the MS, even mild, such as trembling fingers or transient drop of monolateral eyesight? Cause I have.... and I don't know if it's normal or not.
What is your current EDSS score? Thank you, Wishing all the best for you!!