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Top 10 Search Results for "how is thi site not like that on facebook"

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What Is The Correct Time To Vent To Your Friends Here? Should You Make It Clear That You Are?
A MyEpilepsyTeam Member asked a question 💭

I ask this one for several reasons. The first is for those who do not already realize that most friends are ready and willing for you to vent. The second is more important to changing my start of venting by letting friends understand that this is exactly what I am doing.

Finally, it is important to hear from friends who do not want to hear you vent (especially depending upon the topic) and might block you (the equivalent of Facebook's stop following a person's postings. Or they might even… read more

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A MyEpilepsyTeam Member

I only trust my son his family and some friends only Not mom as she tells everyone that almost talk negitive bout me

Mysoline
A MyEpilepsyTeam Member asked a question 💭

when i was a child (10-16) years old i was prescribed but when i left school the doctors changed my medication. why was this when mysoline was controlling my epilepsy. whilst on mysoline i was having 1 maybe 2 fits aweek but since they change my medication my fits have increased and i am unable to work

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A MyEpilepsyTeam Member

I would not pay attention to a School GP, who I think told you to go "Cold Turkey". I know some people stop having seizures naturally. Find a Neurologist or Epileptologist who is very observant, can… read more

Group On Facebook
A MyEpilepsyTeam Member asked a question 💭

I'm creating a group on Facebook but I don't know what to call it. Has anyone got any ideas? It is a group for epilepsy.

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A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member No kidding about the disability...making it stretch is not easy!

How Many Of You Have Reached Out To The Epilepsy Foundation (or The Like) And Ask Them To Spread The Word About This Site?
A MyEpilepsyTeam Member asked a question 💭

Please tell me that I am not the only one urging them to tell everyone with Epilepsy/Seizure Disorder about this amazing site.

It has changed my life to come here and make friends who know exactly what it is like to have a seizure. Don't you want everyone to also receive this gift?

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A MyEpilepsyTeam Member

I about this site from my Neurologist. I've never thought about asking the association to add it. I've thanked my neurologist numerous times for suggesting it. I'm on it daily. I've made online… read more

Hug And Useful
A MyEpilepsyTeam Member asked a question 💭

Just wanted to make a comment. Now I know I am just as guilty of this social media habit as anyone else. But we are in the habit if we are having bad days or good days by just clicking on the hug or useful icons. When really all of us suffering want someone to talk to or just to know that someone is out there listening and will help in whatever way possible. So to my team and everyone worldwide if you want someone to talk to don't be afraid to ask. Turn 2019 into a year where we can be there for… read more

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A MyEpilepsyTeam Member

I'm always available on sms or What's App.... Anyone is welcome to make contact.

Is There A Shortcut To Get To The My Epilepsy Team Site?
A MyEpilepsyTeam Member asked a question 💭

Like an icon or something that will remain on my cell phone home screen i can just tap on an have access to my profile on the site? Like facebook or instagram has ya know?

A MyEpilepsyTeam Member

Add it to home screen

Are You Skilled In The Use Of ZOOM, Skype, Google Meet, Or Any Of The Other Meeting Sites/apps That Offer Free Meeting Options?
A MyEpilepsyTeam Member asked a question 💭

We are looking into allowing expanded options for conversations (live free meetings) with friends on this support site. However, we need more friends who are comfortable with the various meeting sites and their apps. We not only are looking for hosts in the range of time zones of the Earth that we have friends scattered in but also people who are skilled in explaining how to get on to the meetings and use of the features to the friends on here are non-techies.

The idea is to allow live… read more

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A MyEpilepsyTeam Member

I am using Zoom app

Yes. Is There A Site For Spouses? I Am Dealing With A Husband That Doesn't Understand My Seizures.
A MyEpilepsyTeam Member asked a question 💭

Even though we have been together over 20 years, my husband understand my seizures and why I cannot remember things like I used to. I thought there maybe was a separate website for spouses, parents anyone that was not having the seizures, but had to help the person that was.

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A MyEpilepsyTeam Member

Find out through the Epilepsy Foundation if the have any form of counseling or maybe they know of an Org that maybe able to help you husband understand better.

Another idea is to keep up with the… read more

I Need To Sign In On My Computer. I Need Help.
A MyEpilepsyTeam Member asked a question 💭
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A MyEpilepsyTeam Member

i do not know how I fixed it, but I did. The Phone worked first, but there is more room on the Laptop. Thank you.

I Am Leslie3, And Need To Sign In. People Sent Messages And I Cannot Read Them. Please Help. (Email Address Can Only Be Seen By MyEpilepsyTeam Users)
A MyEpilepsyTeam Member asked a question 💭
A MyEpilepsyTeam Member

The link to help for the My Team sites is the following: Here is a link on how to navigate this site and do things here: https://myhealthteams.freshdesk.com/support/home