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Real members of MyLupusTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Please share any reactions or recommendations from your physicians.
Thank you.

September 24
 · 
Reactions
A MyLupusTeam Member

All routine vaccines are recommended for us, and I have taken them all except the HPV (which I was too old to receive). Twice-yearly COVID boosters are recommended for those of us who are immunocompromised, i.e., on meds other than HCQ for our lupus. Sadly, there are still deaths from COVID among older and immunocompromised individuals, so we need the protection.

September 25
A MyLupusTeam Member

I'm usually extra achy and fatigued for a couple days after my yearly flu and Covid vaccines so I plan them for when I know I can rest after. I also have to hold my Methotrexate for the week(per Rhem instruction). Definitely worth it though to be protected.

September 25
A MyLupusTeam Member

Yes, I get them all and have had no adverse side effects.

September 25
A MyLupusTeam Member

I have had all but HPV without any issues. Keep in mind that we all react to vaccines differently.

September 25
MyLupusTeam

Many MyLupusTeam members have shared their vaccine experiences, and while reactions vary, severe side effects are not the norm. The most commonly reported reactions tend to be mild and short-lived, such as:

- Soreness or redness at the injection site
- Mild fatigue or low-grade fever
- Temporary joint achiness

These typically Show Full Answer

Many MyLupusTeam members have shared their vaccine experiences, and while reactions vary, severe side effects are not the norm. The most commonly reported reactions tend to be mild and short-lived, such as:

- Soreness or redness at the injection site
- Mild fatigue or low-grade fever
- Temporary joint achiness

These typically resolve within a day or two. When it comes to COVID vaccines specifically, health experts — including the Lupus Foundation of America — strongly recommend staying up to date. The vaccines are not live, meaning they cannot trigger an infection, and are considered safe for people with autoimmune conditions.

A few important things to keep in mind:
- Timing matters — your doctor may suggest scheduling vaccines when your lupus is stable, not during a flare
- Medication adjustments — some physicians temporarily pause certain immunosuppressants around vaccine time to improve your immune response
- Extra doses may be needed — if you're on immunosuppressive therapy, your body may not respond as strongly, so additional doses might be recommended One important heads-up: live vaccines (like the shingles vaccine Zostavax) are generally not recommended for people with lupus who are on immunosuppressive medications. However, the non-live shingles vaccine (Shingrix) is a different story — always check with your rheumatologist about which version is appropriate for you.

The bottom line? Chat with your care team before any vaccine. They know your specific medications and disease activity best, and can help you time things safely. 💉

September 24

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