MyLupusTeam
yesterday at 23:45. Facebook
“The biggest grievance those with chronic conditions have is that their loved ones often do not believe what they are going through is real, because to others they 'look good.'"

But You Look Good: Living with Disbelief of Invisible Illness and Pain

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MyLupusTeam
02/19/2017 at 00:30. Facebook
Do you get jaw pain? How do you deal with it?

Join discussion HERE: [ Goo.gl Link ]

#Lupus
#Lupie
#LupusWarrior
#LupusAwareness
#Lupies

Jaw Pain & Lupus

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MyLupusTeam
02/17/2017 at 23:00. Facebook
The Worst #Lupus Advice

See what others like you said:

Your Answers: The Worst Lupus Advice (Infographic)

mylupusteam.com
MyLupusTeam
02/17/2017 at 15:00. Facebook
"I’m the one who will have to endure it all. And yet I still can’t rid myself of the lingering feelings of guilt that eat at me, day-in and day-out."

#Lupus #Lupies #fightLupus

Feeling Guilty Because of Lupus

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MyLupusTeam
02/16/2017 at 23:30. Facebook
“I walk because it keeps my joints lubricated and limber and it helps me to keep the remaining bone density I have left because I have osteopenia.”

#Lupus #LupusAwareness #Osteopenia

Living with lupus

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MyLupusTeam
02/16/2017 at 07:45. Facebook
Still awake? :(

Come over to MyLupusTeam.com to discuss lupus and sleep issues.

#lupus
MyLupusTeam
02/15/2017 at 20:30. Facebook
"Think of it as a nonlinear process... People tend to think of self-love as something you figure out and at some point you are done. Some days will be better than others."

10 Tips for Radically Loving Your Body (Disabled or Otherwise)

thebodyisnotanapology.com
MyLupusTeam
02/15/2017 at 00:30. Facebook
The Four Most Common Triggers Of A Lupus Flare:
Weather, stress, exhaustion and nutrition

#Lupus #LupusFlare #LupusAwareness #Lupie #Spoonie

The Honest Truth About Controlling Lupus: Four Common Triggers of Flares

mylupusteam.com
MyLupusTeam
02/14/2017 at 00:35. Facebook
"We would give anything to no longer suffer from chronic pain, and thus to no longer need medication. And our conscientious use of pain medication actually benefits everyone else. Pain medication keeps us out of the emergency room so it’s less busy when you need it."

I use pain medication, but I'm not an addict

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Where do you find the support you need to cope with lupus?

Join discussion >>> [ Goo.gl Link ]

#Lupus #lupie #lupusawareness #fightlupus #lupuswarrior

Finding The Support You Need To Deal With Lupus

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Today I choose to move forward... YOU CAN DO IT!

Love, MyLupusTeam.com
The 9 Most Frustrating Things About Being Chronically Ill
[ Ow.ly Link ]

The 9 Most Frustrating Things About Being Chronically Ill

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Vitamin D Levels Low in People with Severe Lupus, Study Shows
[ Ow.ly Link ]

#Lupus
#VitaminD

Vitamin D Levels Low in People with Severe Lupus, Study Shows

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Only others with #lupus understand what it's like.

Join MyLupusTeam.com for daily online support.
We Try to Look Our Best
“But you don’t look sick” is one of the most common phrases you hear if you have invisible disease. Well yes, we try to look our best even on bad days when our body explodes from pain.

#ChronicPain #Pain #Spoonies #ChronicLife

16 Things People With Chronic Pain Wanna Tell You

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Sleep disturbances and/or poor sleep quality is associated with around 60% of lupus patients.

#Lupus
[ Ow.ly Link ]

LUPUS AND SLEEP - Molly's Fund

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Have you seen our infographic? The many ups and downs of Lupus that people don't see...

Please share!

#Lupus #LupusAwareness #LupusWarrior #Lupie #LupusFighter

Lupus: What People Don't See (Infographic)

mylupusteam.com
I can't stop itching!! What helps?
Read answers from lupies like you: [ Goo.gl Link ]

#Lupus #lupie #lupussucks #LupusWarriors #lupies

I can't stop itching! (Lupus)

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"Hope gives us the ability to make the lifestyle changes we can, to get the rest we need, and to accept the help we deserve."

#Lupus
#LupusWarriors
#LupusAwareness

The secret ingredient to living well with lupus: A dose of hope.

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