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You are here: Home / Fibro Warriors / Fibro Warrior Wednesday – Beverly D

Fibro Warrior Wednesday – Beverly D

Last Updated: August 14, 2013

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

Beverly D, is another member of my local support group. We have such a wonderful group of people in our group, with wide varieties of experience. She was diagnosed in 1998

What lead up to your diagnosis (symptoms, dr visits, etc)?
I had severe headaches, joint pain, confusion, muscle pain, insomnia, extreme fatigue, stomach pains and upset. I went to 18 different doctors over a 5 year period and they “found” nothing.

How long had you been dealing with various symptoms before you were finally diagnosed?
Now that I look back, I believe I have been symptomatic since I was 9 years old. There was a definite trauma: I was raped as a child at 6 and started my periods at the age of 9. From that point, all I can ever recall is being in pain when none of my other friends were experiencing the same. I thought it was my punishment for the rape because I never told anyone and the rapist was a family friend. It was my shame; I am so not bearing that shame anymore for being sexually violated by a criminal. But, as a child, what else was left for me to do.
What was your life like at the time?
I was married with 2 kids in high school and one living on his own. I was working at the time as a Program Analyst, in Government Contracts Management.

How did your family initially handle your illness?
They were clueless, thought I was crazy, and suggested I see a counselor. I did so, just to hold on to my sanity.

How has your family/ work situation changed since Fibromyalgia entered your life?
I have since retired from federal service because I could not function at what I felt was a competent level. I was a program analyst whose job involved high dollar government contracts management. I also suffered several Trans Ischemic Attacks (TIA) which left me with a few deficits. The Fibro fog was horrendous. I now run a small business from my home, paint and craft for enjoyment and do Yoga for relaxation.

What do you feel is the most challenging aspect of Fibro?
People not understanding…that I hurt all the time but at different levels throughout the day. I admit, I LOOK GREAT, but we know everybody says “you don’t look sick”.

Do you have any other co-existing conditions? If so, what are they and how do they impact your Fibromyalgia?
I mentioned the TIAs…I also have asthma, Hypertension, Diabetes, minor heart valve issues and Depression with occasional anxiety. The Fibro seems to feed off of the Depression. I have great days and then I have Depression which I feel physically, as well as mentally. If I am flaring, my blood pressure is spiked.

What (if anything) have you found/ done that has improved your symptoms?
I meditate. I relax, take a soothing bath in Epson salts, slow down, do less, massage therapy and as a last resort, I take prescription pain medicines.

What is the best advice you’ve received regarding Fibromyalgia?
It’s not your fault! If you can move, move, and if you can’t move, rest. Don’t feel guilty.

What was the worst advice that you followed?
Believing that there wasn’t really something wrong with me. One doctor suggested I get a hobby! That I just needed more to do. You can’t print the words I used on my follow-up visit to his office. 🙂

Are you a Fibro Warrior? I’d love to share your story here. If you are willing to share your story, please email me.

1 Comment Filed Under: Fibro Warriors, friendship Tagged With: dealing with fibro, diagnosis, family, interviews, support

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Vicky Jackson says

    August 16, 2013 at 4:56 am

    Thank you for this great interview! It’s helpful to read fibromyalgia stories, to see how each of us learn to cope, etc…Thank you Beverly D and thank you Julie!

    Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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