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"Change your expectations and learn to navigate your “new normal.” This one may be the toughest to accomplish.Your vision of what family life would and should be based on past ideas and hopes might need to be dramatically altered to allow for having an unpredictable illness."

#Lupus
#LupusAwareness

10 Tips for Parents Living with Chronic Disease

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MyLupusTeam
12/06/2016 at 22:30. Facebook
Tips for cleaning when you have debilitating fatigue:

"Having everyone take their shoes off upon entering your home dramatically cuts down on the amount of debris that dirties your floors. It's great for extending the cleanliness of your floors."

20 helpful tips for cleaning & organizing when you're chronically ill

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MyLupusTeam
12/03/2016 at 18:00. Facebook
We're discussing social anxiety and lupus. Join discussion: [ Goo.gl Link ]

#Lupus #Lupie #LupusWarrior #LupusSucks

What To Know: Social Anxiety and Lupus

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MyLupusTeam
12/02/2016 at 23:30. Facebook
"Don’t EVER feel like you are a burden. Lupus is a condition that you cannot control. It is NEVER your fault what you’re going through."

#Lupus
#LupusAwareness
#Lupie

My Story: “I Won’t Let Lupus Beat Me”

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MyLupusTeam
12/02/2016 at 01:24. Facebook
Lupus and Skin Symptoms (Infographic)

#Lupus
#LupusWarrior
#LupusAwareness

Lupus and Skin Symptoms (Infographic)

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MyLupusTeam
12/01/2016 at 00:54. Facebook
We've reached 70,000 members! We are so thankful for all the support shared on MyLupusTeam.com <3

#Lupus #LupusWarriors
Dealing with Lupus (flare ups)

#lupusflare
#lupus
[ Youtube.com Link ]

Dealing with Lupus (flare ups)

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Do you experience bruising with your #lupus?
CHAT with others who understand:

What To Know About Lupus & Bruising

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What did we learn? From the unconcerned ("It's not so bad") to the plain unhelpful ("But you look fine"), advice is hurled at us from friends, family, coworkers, even strangers. While most suggestions are probably well-intentioned, hearing them over and over can make us feel that our lupus is minimized and misunderstood.

Check out our...
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Your Answers: The Worst Lupus Advice (Infographic)

mylupusteam.com
"When hosting a dinner party (or a get together) take the time to share with your Chronically Ill friend ahead of time the ingredients of all of your dishes. This will save your friend any awkwardness of having to ask questions in front of the other guests and feel like a burden at the party."

15 Ways to Help a Friend with a Chronic Illness during Thanksgiving

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Toni Braxton Performs With Heart Monitor

[ Ow.ly Link ]
#Lupus #LupusWarrior #FightLupus

Toni Braxton Performs With Heart Monitor

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Join the fastest growing online support network for people with lupus: [ Mylupusteam.com Link ]

Lupus Support Online - MyLupusTeam

mylupusteam.com
Lupus: There’s ‘hope after diagnosis’

#lupus #lupuswarrior
[ Ow.ly Link ]

Lupus: There’s ‘hope after diagnosis’

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What do you do when you start sweating for no apparent reason whatsoever? :)

Join our lupus discussion: [ Goo.gl Link ]

#Lupus #LupusWarriors #Lupie #FightLupus

Sweating and Lupus... What's The Deal?

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We love Dorothy Height:
"Grandmother, business woman, civil rights activist, and lupus educator. Unless you know her personally, you may be pigeonholing her as 'the lupus lady.'"

#Lupus #LupusWarrior #FightLupus

Dorothy Height — more than ‘the lupus lady’

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#LUPUS:
"Imagine feeling ice picks on your ears, a hammer pounding your head, vice grips on your knees and fire on your back."

Locals share stories of living with lupus

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Only others with #lupus understand what lupus is like.

Join MyLupusTeam.com for daily online support.
'Dry eye' linked to chronic pain syndromes
[ Ow.ly Link ]

'Dry eye' linked to chronic pain syndromes

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