Or so the saying goes. This photo was on MCS Gal’s blog yesterday. The picture says it all to me! It is how I have felt many times, just plain invisible despite the mask I wore on my face when outside my home. I hope you will take a few minutes to visit MCS Gal’s blog and read this post. We need to keep sharing.
![invisible-6_l[1]](https://allergictolifemybattle.wordpress.com/wp-content/uploads/2013/09/invisible-6_l1.jpg?w=208&h=300)
allergictolifemybattle 
Amen!!!!!
Reblogged this on sondasmcschatter and commented:
AMEN!!!!!
Oh, yes, I know how that feels!
The picture that MCS Gal posted just resonated with me so much that I had to share it and her post.
This is how i felt after getting started on seizure medication. The first church member that I mentioned having epilepsy to, backed up one step. I wanted to yell at her, “I’m not contagious!” When I used the word ‘seizure’ no one seemed to care. Today I read a blog which made the comment that we should not see our selves in a bad light. Then I remembered a Bible verse, Proverbs 23:7–as a man thinketh so is he… (Those are not the exact words, but close. I could not find a NT reference) I need to stop thinking of my problems, and start thinking of the positive side.
I love those words. It is hard to not think of our problems but it helps to find something else to do to take our minds off them. I embroider, read, learned how to crochet a scarf last winter and made several, and this year have learned how to knit a really cool looking scarf. I ran out of the yarn and am back to embroidering until the yarn arrives. I need to take a few minutes and comment on my blog post about speaking with my therapist and her help she gave me. Maybe tomorrow in between prepping for Thanksgiving.