I just wanted to say that I am currently having the Ocrevus treatment and am over 50, so I was given the opportunity to have the Covid Vaccine, which I was so pleased to have.
The NHS are amazing for the system they have organised to make this a safe and speedy operation.
As for the vaccine, I have to say that I suffered quite a horrible headache for about 4 days and my body felt like it had been 10 rounds with Mike Tyson, but all said and done, this was nothing compared to what may have been the symptoms should I have contracted Covid.
I wanted to write this as there seems to be so much negativity around the whole situation, the way that I am looking at it, is that I am here, I am able to have dinner with my husband and chat to my children and am looking forward to welcoming my first grandchild into the world. This seems very mundane, but they are the things that make me smile and appreciate being alive.
I hope that everyone that is on here, is keeping safe and avoiding this awful virus.
Sending positive vibes to you all, thank you for the chat and information that has kept me sane through not only this current situation, but also through my MS journey so far. Keep up the good work everything you post and your replies are so valuable.
Michelle
Interesting article about the various vaccines for coronavirus from the MS Research Blog:
The best protection against anti-Vaxers…is knowledge. – Multiple Sclerosis Research Blog
MULTIPLE-SCLEROSIS-RESEARCH.ORG
Want to learn about the new vaccine in the news. Watch the video from Dr Professor Roger Seheult from Webcram below. The information starts at 2min and is 20minutes long. The first...
This is very early days, but might offer some hope for the future?
BioNTech Vaccine Treats MS in Mice Without Dampening Immune System
MULTIPLESCLEROSISNEWSTODAY.COM
BioNTech’s experimental non-inflammatory vaccine — designed to dampen the abnormal immune responses seen in multiple sclerosis (MS) against myelin — delayed the onset and...
I was diagnosed with MS 10 years ago, I have relapse and remitting MS. Thankfully I have very mild and brief relapses, and I’m not receiving any treatment for my MS.
I have recently met a partner who has told me they have chronic hepatitis B, which has left me with a huge dilemma. If I was to stay with my partner I’d need to receive the Hepatitis B vaccine to safeguard myself, but I’m uneasy with the idea of having the Hepatitis B vaccine as the link between the vaccine and MS is negative. And I wouldn’t want to do anything that could cause my MS to progress.
I’d be grateful if I could hear others experiences with their MS and having the Hepatitis B vaccine please.
Hi everybody
Just wondering how you r all feeling about the swine flu - I wasnt paying too much attention to it before.... as it seemed so far away... and i didnt want to freak myself out about it...
But its a little scarey now and just wondered will people with ms be recommended to get the Swine flu jab...
I have never had a flu jab as my doc said theres a chance it can aggravate ms symptoms/ relapse etc...My bosses wife has ms and her Neuro told her not to take it... but all Neuros say different..... What to do?
anyway just like to see how you all think about this.... you guys always know best!!
Keep groovy
Love Lindaxx
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