Author Archives: Melynda Poss

The If’s Have Had Me…

Do you ever live life wondering ; “what if?” “only if?” “I should have…” “Lord, if you, I will…” ?  You are not alone! This chick does it all the time.  You know why? I am imperfect, faulty, whatever you … Continue reading

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Celebrating One Year…

June 22, 2016 was a day I will never forget. I was driving to work just like every other day and I took a sip of tea as I was waiting to get on I-20. In that instant I knew … Continue reading

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Turning on a dime….

Myasthenia Gravis is a tricky disease no doubt about it. I was not feeling well Friday just simply worn down. Saturday morning I woke up after a good rest and still felt worn down. I had two picnics – one … Continue reading

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I Call It Progress…

June is Myasthenia Gravis Awareness Month and while most people have never heard of it I live it every second of every minute of every day! I know that sounds monotonous but there is not a second in the day … Continue reading

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Happy Birthday Buddy!

Today is an extraordinary day in our household. It was 17 years ago today when I was only 34 weeks pregnant Charles Adam Poss made his first appearance into this crazy world we live in. I can remember every second … Continue reading

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A Father’s Love Never Dies…

There is one thing that has brought me peace and let me know everything would be ok – climbing in my Daddy’s lap and him just holding me. The comfort in his big belly, the shaking of his jiggly legs … Continue reading

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A Magical Night…

Tonight my baby boy goes to his Junior Prom. He has worked hard on the prom committee to decorate and raise money. You see Adam is my quiet child so this turn around in his has been a wonderful fun … Continue reading

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Resting….

Here I sit day three in the hospital waiting on my last IVIG treatment. The funny thing is if my insurance company had cooperated I could be getting this at home or out patient but because of their lack of … Continue reading

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I’m A Turtle & It’s OK!

Yes, you read that right, I am a turtle in life right now. I piddle along doing what I can at a slow pace especially if it requires physical energy. It may take me two days but, I will eventually … Continue reading

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When you can’t speak…

This past week has been one of frustration, tears & just simply asking The Lord to bless those who are caring for me. I am sad. I hate this disease but I know that God has a plan. I know … Continue reading

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