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MyEpilepsyTeam
yesterday 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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MyEpilepsyTeam
12/03/2016 at 18:15. Facebook
How do you handle your condition at work? Is your boss understanding?

Join our #epilepsy discussion: [ Goo.gl Link ]

#EpilepsyWarrior
#FightEpilepsy
#EpilepsyAwareness

How Do You Cope? Epilepsy At Work

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MyEpilepsyTeam
12/02/2016 at 22:45. Facebook
"Medications work wonders and give people a normal life; however, they are also extremely hard on one’s body. Much of the time-fighting epilepsy is also fighting the medication that is fighting the seizures…"

#Epilepsy
#EpilepsyAwareness
#PurpleForEpilepsy

There is much more to epilepsy than meets the eye

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MyEpilepsyTeam
12/02/2016 at 01:20. Facebook
"As hard as epilepsy is on me, I think it’s harder on my family. They have to watch when I lose consciousness. They are the ones who see me seize."

#Epilepsy #EpilepsyAwarenessMonth

Don’t Look Now, It’s a Seizure!

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MyEpilepsyTeam
12/01/2016 at 00:53. Facebook
We've reached 30,000 members! We are so thankful for all the support shared on MyEpilepsyTeam.com <3

#Epilepsy #FightEpilepsy
Being Your Child’s Pharmaceutical Historian
[ Ow.ly Link ]

Being Your Child’s Pharmaceutical Historian

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Interesting podcast about the creator of the #KetogenicDiet: The Man Who Cured Everything

#epilepsy
[ Ow.ly Link ]

The Man Who Cured Everything

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We're talking about lifestyle changes after an #epilepsy diagnosis. Join us and CHAT with others who understand:

Things That Changed After My Epilepsy Diagnosis

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From the unconcerned ("It's all in your mind") to the plain unhelpful ("Just don't stress"), 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 epilepsy is minimized and misunderstood.

Check out our infographic:

#Epilepsy
#Seizures
#Epileptic...
View details ⇨

Your Answers: The Worst Epilepsy Advice (Infographic)

myepilepsyteam.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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Emily’s Perspective: Coping Styles

[ Ow.ly Link ]
#epilepsy #epilepsywarrior

Emily's Perspective: Coping Styles

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

Epilepsy Support Online - MyEpilepsyTeam

myepilepsyteam.com
What lifestyle changes have you made since becoming diagnosed?

Chat with others like you --> [ Goo.gl Link ]

#Epilepsy #EpilepsySucks #EpilepsyWarriors #FightEpilepsy

Things That Changed After My Epilepsy Diagnosis

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"There are a million similar, and a million different stories of how families are dealing with epileptic children. Many of us spend all day counting seizures and trying to keep our kids safe."

#Epilepsy #EpilepsyMom #EpilepsyDad

My Typical Day As A Parent Of A Child With Epilepsy - Epilepsy Dad

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Only others with #epilepsy understand what it is like.

Join MyEpilepsyTeam.com for daily online support.
Epilepsy and Your Sex Life

#Epilepsy
[ Ow.ly Link ]

Epilepsy and Your Sex Life

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Members say the social interaction on MyEpilepsyTeam can boost your spirits.
It's free ---> MyEpilepsyTeam.com

#epilepsy