- Home
- Share
- Forum
- Lupus Forum
- Living with lupus
- COVID-19 and Lupus: How is lockdown and the pandemic impacting your lupus?
Patients Lupus
COVID-19 and Lupus: How is lockdown and the pandemic impacting your lupus?
- 155 views
- 12 times supported
- 10 comments
All comments
eleventwelve
Good advisor
eleventwelve
Last activity on 07/05/2020 at 09:28
Joined in 2016
9 comments posted | 9 in the Lupus Forum
Rewards
-
Good Advisor
-
Contributor
-
Explorer
@Courtney_J I was actually contacted by the NHS to inform me that I'm at high risk. I had heard they would be doing that, but I didn't think I would be contacted so quickly! They've told me to 'shield' myself for 12 weeks! I'm not excited about it as I don't think anyone enjoys being cooped up indoors, but I know that it's for my protections. Trying to see the bright side of things.
wolfloup
Good advisor
wolfloup
Last activity on 11/01/2023 at 01:06
Joined in 2016
8 comments posted | 6 in the Lupus Forum
Rewards
-
Good Advisor
-
Contributor
-
Explorer
I've heard that there's going to be a run on plaquenil because of the pandemic. Has anyone heard anything about this? Has anyone had a hard time getting it at the pharmacy? I will need a refill soon so I'm a bit worried...
KPangela
Good advisor
KPangela
Last activity on 20/11/2024 at 14:32
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 was contacted by my GP a week ago and got a letter on.. 31march. A week earlier I'd put myself onto the Covid19 government list, got a text from them today 01april
Shielding is sort of working, we're successfully using separate loos during the day and night. When we're in a room together we've got a 2m ish space, window open when it's not cold. Sleeping in separate beds, bedroom is a non starter. Eating food also the same as I don't want to eat on my own! My son hasn't been in any shop, his last mix was with his mates at school, and my husband only goes out once a week for shopping and my meds. He uses a sanitizer every time he's been in a shop.
I feel safe with what we, as a Family are doing.
See the signature
Karen
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 everyone, how are you doing in self-isolation?
Hello @wolfloup, thank you for your comment. Have you seen our recent article on hydroxychloroquine and the impact that its use for treating COVID-19 is having on lupus patients? In it we summarise the results of our survey on the subject and share what our Carenity members are experiencing across the globe. I think you may find it interesting!
Plaquenil as a treatment for COVID-19: What are the consequences for chronic patients?
Feel free to take a look and share you thoughts in the comments below the article!
Take care,
Courtney
See the signature
Courtney_J, Community Manager, Carenity UK
eleventwelve
Good advisor
eleventwelve
Last activity on 07/05/2020 at 09:28
Joined in 2016
9 comments posted | 9 in the Lupus Forum
Rewards
-
Good Advisor
-
Contributor
-
Explorer
@Courtney_J Thanks for the article, it was interesting to read the results of something that I filled out and see where what I'm going through is similar to others' experience. Hope everyone is doing well and staying sane through this!
ClaireTF
ClaireTF
Last activity on 02/06/2020 at 18:18
Joined in 2016
Hi there, I actually had a problem getting my plaquenil the other day, the chemist was only able to fill half of it... I'm guessing it has to do with Trump and all of that nonsense from a few weeks ago. Has anyone else had a problem?
I have a lot of anxiety and it's hard to stay alone with just me and my thoughts. Usually I'm don't go out much but being forced to self-isolate is very different. It's like a cage and the outside seems tempting but scary in the same time. Not sure if I make any sense...
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
@ClaireTF Hello ClaireTF, thank you for commenting. I'm sorry you had a problem getting your prescription. Were they able to fill the rest later?
Has anyone else had a problem with this? How are you during in lockdown?
@upnorthhere @lupus79 @iwillbeatthis @allie1983 @Shellington79 @Kelly246 @Jack.Mcm @Holly12 @Jazzib58
Take care,
Courtney
See the signature
Courtney_J, Community Manager, Carenity UK
robjmckinney
AmbassadorGood advisor
robjmckinney
Ambassador
Last activity on 19/11/2024 at 19:37
Joined in 2015
596 comments posted | 14 in the Lupus Forum
47 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Committed
-
Explorer
-
Evaluator
Hi All,
No issues with my wife's medicines and despite a flare up issues there has been no problems, anti-biotics covered the infections. No problems with getting quinine only I had issues with some diabetic medicine, my brother running short on his injections as well. But my wife had a long phone call from our practice as a follow up for the 'vulnerable patients' status but we had no issues. So all in all in isolation awaiting our release so we can go to our caravan in Norfolk, we can isolate there as well as at home. One thing the GP did state that the lock down was to be extended for the vulnerable and my wife is not allowed out the house, not even the garden total isolation. Thought it a bit OTT and we do go for a short walk with the dog in the evening when nobody is about, getting some nice fresh air!
Stay safe!
See the signature
robjmckinney
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 everyone,
How are you today?
How are you holding up in lockdown? Have you noticed any flares or changes in your lupus? Is it better? Is it worse? Have you heard anything about the vaccine?
@amanda397 @Cindy1 @Tjsharples @upnorthhere @lupus79 @iwillbeatthis @allie1983 @Shellington79 @Fay#:o'Connor @Kelly246 @Aineokeeffe @Jack.Mcm @Holly12 @Jazzib58 @Cazza55w @Jooliver @Lilread92
Feel free to share! We are all here to help each other!
Take care,
Courtney
See the signature
Courtney_J, Community Manager, Carenity UK
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...
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
14/12/2022 | Testimonial
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
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
The coronavirus pandemic has spread very rapidly and some strict new measures have been taken since yesterday, Monday, 24 March. Covid-19 affects everyone, regardless of age or background. But as we know, not everyone reacts in the same way to this virus.
The purpose of this discussion is therefore to allow you to discuss the virus in the context of Lupus in particular.
Have you had any specific recommendations from your doctor regarding your treatment? Have you taken any particular precautions?
Finally, how do you handling social distancing? How do you spend your days?
If you haven't already done so, feel free to consult the latest article in our Health Magazine which deals with the Coronavirus and chronic diseases.
Take care,
Courtney
@upnorthhere @lupus79 @allie1983 @iwillbeatthis @Shellington79 @Kelly246 @Jack.Mcm @Holly12 @Jazzib58 @Cazza55w @Jooliver @Lilread92 @LouiseElcross @Emma1981 @Linzijc @Smelly @MrsB007 @Sandyk @CeriPrice @BeverleyAnnemcc @Debrahenden @Aideenof @Susannah16 @Jackleo1 @Marc18 @Julilonpe @Raine29 @Sofy786 @lupusk @Kazz76