- Home
- Share
- Forum
- Lupus Forum
- Living with lupus
- Will you or have you received the COVID-19 booster vaccine?
Patients Lupus
Will you or have you received the COVID-19 booster vaccine?
- 9 views
- 0 support
- 3 comments
All comments
Courtney_J
Community managerGood advisor
Courtney_J
Community manager
Last activity on 13/10/2022 at 16:47
Joined in 2020
1,280 comments posted | 19 in the Lupus Forum
10 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Committed
-
Explorer
-
Evaluator
Hello @KPangela, thank you for opening this discussion. What a frustrating mix-up! Do let us know what your rehumatology team says.
Has anyone else had your booster jab yet? Have you had any issues getting it or any reactions afterwards?
@Jude13 @Viny76 @amanda397 @Tjsharples @upnorthhere @lupus79 @allie1983 @iwillbeatthis @Shellington79
Feel free to share here!
Take care,
Courtney
See the signature
Courtney_J, Community Manager, Carenity UK
lesjames
Good advisor
lesjames
Last activity on 25/11/2024 at 08:59
Joined in 2016
13 comments posted | 2 in the Lupus Forum
Rewards
-
Good Advisor
-
Contributor
-
Committed
-
Explorer
-
Newsfeeder
I have had my third jab and now have to wait for 24 week to have the Booster. I have also had my flu jab.
KPangela
Good advisor
KPangela
Last activity on 22/12/2024 at 15:16
Joined in 2016
83 comments posted | 14 in the Lupus Forum
9 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Committed
-
Explorer
-
Evaluator
I continue to have major issues in trying to get my third booster vaccine because I'm immunosuppressed it's called a third Primary not that it makes a lot of difference because my second job was 6 months ago. Anyway the irony is my husband has been able to book his booster jab I can't even get mine!
See the signature
Karen
Give your opinion
Members are also commenting on...
Living with diseases affecting muscles, joints and-or skeleton
Life after a joint replacement: Share your experiences and advice!
Unregistered member
I had a hip replacement 16 months ago due to osteoarthritis. I can honestly say it was the best decision I have ever made. Yes I was not looking forward to everything post op, but I am now 100% mobile and after not being able to walk any distances I now enjoy walking again and I've managed to lose 2.5 stones. Totally pain free and I've had lots of comments about how much happier I look - my face was obviously showing my pain. If you have any questions please ask!
See the best comment
Living with diseases affecting muscles, joints and-or skeleton
Life after a joint replacement: Share your experiences and advice!
Unregistered member
I had a hip replacement 16 months ago due to osteoarthritis. I can honestly say it was the best decision I have ever made. Yes I was not looking forward to everything post op, but I am now 100% mobile and after not being able to walk any distances I now enjoy walking again and I've managed to lose 2.5 stones. Totally pain free and I've had lots of comments about how much happier I look - my face was obviously showing my pain. If you have any questions please ask!
See the best comment
Articles to discover...
22/11/2024 | Nutrition
Lupus diet and meal planning: Tanya’s top tips to reduce inflammation and manage symptoms
03/11/2023 | Testimonial
Lupus: "We didn’t choose lupus, but we CAN choose our journey"
23/08/2023 | Testimonial
Dietitian Tanya helps the Lupus community to reduce their symptoms with diet and healthy living.
10/05/2023 | Advice
05/09/2018 | Testimonial
06/02/2019 | Advice
Photo testimonial: Years of diagnostic uncertainty facing Ehlers-Danlos Syndrome
Subscribe
You wish to be notified of new comments
Your subscription has been taken into account
KPangela
Good advisor
KPangela
Last activity on 22/12/2024 at 15:16
Joined in 2016
83 comments posted | 14 in the Lupus Forum
9 of their responses were helpful to members
Rewards
Good Advisor
Contributor
Messenger
Committed
Explorer
Evaluator
I've just had a letter from my rheumatology team informing me that I'm entitled to the 3rd vaccination. I can get this 8 weeks after my 2nd jab (given 6 months ago!).
I've been having trouble booking my booster, but I'm informed by 119 that (3 times) the my NHS number has the wrong date of my 2nd jab, so I no mention of the 3rd!?
My plan is to call my rheumatology team Monday,
Frustration doesn't cover it.