I had my π· shot a month ago, but before getting it I called my ms π¨πΌββοΈ and Aubagio nurse and was advised NOT to have the new shot for over 65. Both said that there was no info with it and people with ms. So just a note π I had the regular βοΈ
π· Flu Shot: I had my π· shot a month ago... - My MSAA Community
π· Flu Shot
Good to know. I was told that when you have the Crevus fusion you canβt have a live flu shot. I was also told by a nurse that you should relax your arm so you donβt tighten up the muscle.
Smart move to check with your Dr's 1st Kenu
What kind of pup π is that? And what's it's name?π He/she looks little?
J π
Thatβs Rozy, she is a Goldendoodle and is three years young. She is 80 pounds of pure lovebug. She loves everyone and thinks sheβs a lap dog. She is so sweet π€
She is adorable! 80lbs lap dog π π³π Kenu She looks like she could be a marshmallow ?π
J π
Thanks, Kenu . I assume you've had no problems since getting the shot? π
Kenu, it's Fancy1959. Thanks for letting everyone know what you were told from your nurse. As always gang it's best to consult with your MS neurologist before taking any vaccinations to see how they will work, not work, or provide bad results because of the therapy you're on.
Because I have begun the Ocrevus therapy I am not allowed to take the flu shot in any form. The way my therapy works is it wiped out half of my immune system, the B cells. That leaves need more vulnerable to attack from viruses. This is the reason that I suggest talk to your doctor because I've always taken the flu shot religiously every year and I wish I could do it this year but I understand that it's best if I do not take it.
Thank you for the informative post and it's always good to know from individuals little items like this in order to ask your doctors and others about. Great job and glad you have become a vital part of our family and chat room. Talk to you soon. Fancy
Fancy1959 Just FYTI, I had the first doses of Ocrevus in Aug., saw an MS neuro. the beginning of Sept., and he gave the OK to have the flu shot (in fact he encouraged all his patients to get the flu shot), so I had one the end of Sept. with no problems at all. I guess every one is different including Drs.!
I never get flu shots. My internist feels I am comprised enough having MS. I never talk to my neurologist about it but maybe the ms specialist I am starting with will have an opinion. The only shots I have received in 12 to maybe 40 years are the two new pneumonia vaccines not live so Iβm told. I might be interested in the new shingles vaccine if it is indeed not live. I have heard it is painful.
Iβm not taking Aubagio, but had the over 65 flu shot on Oct 1, no problems, it has no live virus in it. I had the Tpap (tetanus/whooping cough) 2 weeks ago, no problems. My go doc thought it might be a good thing. Between my gp & MS neuro, they are taking very good care of me! I got both vaccines at Walgreens, flu was free, $25. For the Tpap. Best to you!
Thanks for the info π
Hi Kenu, I am taking Aubagio and I took Flu shot 2weeks ago without any problem for my surprise, and also shot for Hepatite A that I was not immune yet. I did not had any reaction, I guess because Aubagio control virus. I did not take any flu vaccine for over 10years because I always had bronquite. This time, nothing happened. Good!π
I'm 68yrs, have had MS for ~40yrs, seem sensitive to most chemicals entered in my system, however, had no problem or reaction to the flu shot I had 2 months ago.
Hi there, do you take any therapy for MS?
Yes Aubagio for last ten months, been good so far.π€
Is that an infusion? Do you have the risk of PML? Like so manyπ¬
No, itβs a pill once a day. Donβt miss the infusion and shots I did in the past. Nice change, hope it keeps working.ππ
No I have had SPMS for about 20 yrs.
I had flu shot pneumonia shot ad shingles shot with no problems. Iβm doing Plegridy injections.
Donnie