Epilepsy Talk

“Time Out” | May 11, 2018

I’ll be off the web from Friday 5/11 — Wednesday 5/16, spending some quality “together time” with my niece.

I’m sorry if any of my responses are delayed.

Please take care of one another.

I’ll be thinking of you…

 

 

Posted in Epilepsy
Tags:

21 Comments »

  1. Hope you have a great time! 🙂

    Liked by 1 person

    Comment by Jackie Moore — May 11, 2018 @ 6:57 AM

    Reply

  2. You do so much for us…Have a wonderful visit with your niece.

    Liked by 1 person

    Comment by Bert Duke Hudson — May 11, 2018 @ 7:01 AM

    Reply

  3. I recently read that someone with Epilepsy wanted to have “I am an epileptic” tattooed on themselves, any thoughts on this one?

    Like

    Comment by Elaine Howell — May 11, 2018 @ 7:31 AM

    Reply

  4. All of us need a GOOD TIME OUT, not only when we’re unconscious / time out from a grand mal seizure.

    Liked by 1 person

    Comment by C D — May 11, 2018 @ 7:34 AM

    Reply

  5. have a lovely time and “switch off” from all of the pressures of helping all of us!

    Liked by 1 person

    Comment by Margaret Hay — May 11, 2018 @ 8:02 AM

    Reply

  6. Enjoy your quality time with family also Happy Mothers Day God Bless ❤

    Liked by 1 person

    Comment by Maria — May 11, 2018 @ 8:40 AM

    Reply

  7. Happy Mother’s Day to you too, Maria!

    Like

    Comment by Phylis Feiner Johnson — May 11, 2018 @ 10:35 AM

    Reply

  8. Phyllis
    Hope you thoroughly enjoy yourself. Your column is so appreciated! We’ll all be here when you’re ready.
    Much love to you!

    Like

    Comment by Eve Quigley — May 11, 2018 @ 11:21 AM

    Reply

  9. Have a wonderful time with your niece.You give so much to this wonderful community,thank you 💐🌟

    Like

    Comment by Berenice — May 11, 2018 @ 4:30 PM

    Reply

  10. Have any of my friend out there have family member tell you that you blame them for your illness. I was diagnosis at age 48 and know nobody can fix it. I was just wondering if any one have had family who just cant except your seizures or look them up.

    Liked by 1 person

    Comment by starlene L roe — May 13, 2018 @ 9:32 AM

    Reply

    • Unfortunately many of us are in the same boat.

      My mother wouldn’t even say the “E” word and treated me like a pariah.

      But somehow I made it through with grit and determination.

      Try to find a support group. Surround yourself with positive friends who accept you as you are.

      Like

      Comment by Phylis Feiner Johnson — May 15, 2018 @ 10:45 AM

      Reply

  11. We are going to miss you.
    In any case, have a great time.

    Liked by 1 person

    Comment by BahreNegash Eritrea — May 15, 2018 @ 3:40 AM

    Reply

Leave a Reply

Fill in your details below or click an icon to log in:

Gravatar
WordPress.com Logo

You are commenting using your WordPress.com account. ( Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. ( Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. ( Log Out /  Change )

Cancel

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

    About the author

    Phylis Feiner Johnson

    Phylis Feiner Johnson

    I've been a professional copywriter for over 35 years. I also had epilepsy for decades. My mission is advocacy; to increase education, awareness and funding for epilepsy research. Together, we can make a huge difference. If not changing the world, at least helping each other, with wisdom, compassion and sharing.

    View Full Profile →

    Enter your email address to follow this blog and receive free notifications of new posts by email.

    Join 3,249 other subscribers
    Follow Epilepsy Talk on WordPress.com
%d bloggers like this: