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Lupus Survivors Profile
Lupus Survivors

@lupussurvivors

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Empowering lupus survivors by sharing our perspectives on the impact chronic illness has had on our mind, body, and spirit. #lupussurvivors

Joined March 2009
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@MyLupusTeam
MyLupusTeam
2 months
Chances are those with #lupus have grappled with the question of managing symptoms at home or going to the ER during an apparent flare-up. Check out some guidelines around the topic here that may help making a decision easier: https://t.co/gyomIQGrO1
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mylupusteam.com
“Should I stay or should I go?” Chances are you’ve grappled with that question during an apparent lupus flare, trying to suss out if your symptoms could be
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@MyLupusTeam
MyLupusTeam
2 months
Many people with #lupus notice that they don’t feel well after drinking alcohol, and these unpleasant side effects can linger for days or trigger a flare-up. Learn more here about the impact of alcohol on lupus symptoms: https://t.co/3lUNWbqPAU
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mylupusteam.com
Many people with lupus notice that drinking alcohol makes them feel unwell, and these unpleasant side effects can linger for days or trigger a flare-up. Dr
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@MyLupusTeam
MyLupusTeam
2 months
Most #lupus symptoms fall within the broad categories of skin and hair symptoms, pain, generalized symptoms, neurological symptoms, and symptoms that affect the blood or urine. Learn more about symptoms that could occur here: https://t.co/iHDsXT36vn
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mylupusteam.com
Systemic lupus erythematosus (SLE, also known as lupus) is an autoimmune disease. This means the immune system makes proteins called autoantibodies that ca
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@LupusOrg
Lupus Foundation of America
2 months
We’re 2 weeks away from Lupus & You: After Dark! This event will take on the often-overlooked topic of sexual health and #lupus, including how menopause can affect intimacy, confidence, and connection. Don’t miss this candid, empowering conversation: https://t.co/uazFjhuA3p
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@PainNewsNetwork
Pain News Network
2 months
Medicare patients in 6 states who have chronic pain will soon have some treatment decisions made by AI. Medicare is trying to reduce healthcare costs by denying coverage for "low value" treatments like epidural steroid injections & spinal cord stimulators.
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painnewsnetwork.org
By Pat Anson Medicare patients in six states who need epidural steroid injections, cervical fusions, spinal cord stimulators, arthroscopic knee surgery and other treatments for chronic pain will soon...
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@FibroBloggers
Fibro Bloggers
2 months
The first time you get a fibro flare it can be scary. You are going along in your day to day life trying to cope with your fibro symptoms of fatigue, pain, brain fog, sleep problems & suddenly you feel like you have been run over by a bus. It's a flare! https://t.co/8emfIZAbyU
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@LupusOrg
Lupus Foundation of America
2 months
💜 As September ends, we reflect on all your support has made possible & prepare for the year ahead. Your gift before Sept 30 lays the foundation for breakthroughs to come—creating better treatments, brighter outcomes & hope for a cure. 🌟 Give today: https://t.co/r8YiG3PZBL
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@MyLupusTeam
MyLupusTeam
4 months
Hair thinning with #Lupus? 😟 Biotin is often recommended, but does it actually work? Here’s what you need to know about this supplement: https://t.co/qkKCr82ira
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mylupusteam.com
Thinning hair is a common concern for people with lupus, including systemic lupus erythematosus (SLE), the most common type of lupus. If you’ve ever Googl
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@lupussurvivors
Lupus Survivors
3 years
Results of the MyLupusTeam survey identify members' most common lupus symptoms: fatigue, painful swollen joints, sleep problems, pain, and skin rashes. #lupus #autoimmuneillness #lupusawareness #lupussurvivor
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mylupusteam.com
Lupus can come with a wide array of symptoms, including fatigue, insomnia, and skin rashes. In a survey of more than 500 members of MyLupusTeam, respondent
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@lupussurvivors
Lupus Survivors
3 years
Abortion bans threaten access to an inexpensive drug used to treat lupus. #methotrexate #lupus #autoimmuneillness #lupusawareness #lupussurvivors
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@lupussurvivors
Lupus Survivors
4 years
People with lupus are at higher risk of depression and anxiety because of all the stressors a chronic condition can bring on. Here’s how to cope. #lupus #autoimmuneillness #lupusawareness #lupussurvivors https://t.co/dkob6W9xlm
everydayhealth.com
Managing a chronic condition like lupus can be stressful. Here’s what to know about the risk of mood disorders and how to manage mental health.
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