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You are here: Home / Fibro Warriors / Fibro Warrior – Sarah Ostrin

Fibro Warrior – Sarah Ostrin

Last Updated: September 23, 2015

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.

This week we are getting to know Fibro Warrior, Sarah Ostrin of Salem, Oregon (USA). She’s 29 years old and was diagnosed in 2010 at the age of 23.
Tell us a little about yourself:
I am 29 years old, married with 2 step children, I have two jobs one as a part-time certified veterinary technician and my full-time job as a rehabilitation practitioner (animal physical therapist) at our college of veterinary medicine. I have 2 dogs (a black lab and a dachshund), 3 cats, a goldfish, and a guinea pig. I enjoy spending time with my family watching movies and crafting, especially re-purposing things.
Sarah - Fibro Warrior
What lead up to your diagnosis?
I was having trouble sleeping and was recommended to have a sleep study done to check for apnea. My results showed no apnea but that I woke up every hour because my heart rate would sky rocket which they interpreted as being from pain. From there I was administered the Fibro tender point exam and found I had 16 of 18 positive points. I was then given info on Fibromyalgia and was shocked how many symptoms I had that I didn’t realize were not normal things a person experiences.
How did your family initially handle your illness?
My family wasn’t quite sure what to think about it. I received sympathetic feelings and understanding but no one really understood what it meant including me.
What do you feel is the most challenging aspect of Fibro?
The hardest part for me is having no energy. I sleep horribly, on average about 4hrs a night and never consecutively. Working full-time with a family and other obligations is difficult when I constantly feel fatigued.
Do you have any other co-existing conditions?
I was diagnosed with patellar dislocation disorder at 5yr old. (knee caps are not placed properly due to curved femurs and shallow grooves in my femur causing them to pop out at any moment even when sitting and just moving my leg in and out). I also have anxiety and insomnia disorders which have worsened since my Fibromyalgia pain started. I believe that my other conditions have been beneficial to me dealing with my Fibro. I know that’s odd to say but I think since I had been dealing with constant pain from my knees and lower body my whole life I didn’t recognize my Fibro pain as “abnormal.” I thought it was just because of my knees and I had to deal with it and move on. I wanted to be normal as a kid and play sports, etc. so I just adjusted and didn’t let it hold me back. I have taken that  attitude to help me deal with my Fibro pain and issues.
What (if anything) have you found/ done that has improved your symptoms?
Finding ways to sleep has been the biggest help to Fibro pain. I use ear plugs at night which seems simple but makes a huge difference in how much I wake up. I also use essential oils like lavender to help calm and ease me to sleep. I do take medications like tramadol, gabapentin, escitalopram, trazadone, vitamins, and probiotics as well on a daily basis.
How open are you with friends & family about your illness & symptoms?
I don’t care if people know I have an illness but I try not to put it in the forefront with strangers. My family and friends all know my diagnosis and are very understanding when I say I’m having a “bad pain day”. I still feel like they don’t quite understand what it’s like but they are extremely supportive, especially my husband. I’m not sure I could do it all without him.
What is the best advice you’ve received about Fibromyalgia?
I wouldn’t say I have received a lot of advice about Fibro except to try and not stress about things, which I try my best to not do. I will say I am more then grateful for the spoon theory because it was the best thing to help my family understand what my daily life is like and was an eye opener for me as well.
The Spoon Theory has helped my family understand what daily life is like. #SpoonTheory Share on X
Sarah What was the worst advice that you followed?
I was told to try a few different medications which worked for other people but did not work for me at all!!
What is your favorite way to cope with your life as a spoonie?
I love my alone time to calm down. It’s hard to find, but even just taking a long shower or diving into a great book and ignoring the world have been really helpful. I also enjoy reading blogs and posts from others so I know I’m not in this alone.
What is it that inspires you to keep going, despite your illness?
Life. I manly have one chance to do as much as I can with this life and I don’t want to miss out on anything. My family friends animals food adventure I want to be a part of everything
What is the most important piece of advice you would give to someone newly diagnosed with Fibro?
Don’t overload yourself with medications, it’s hard to get away from them once you start. Try holistic approaches and try to simplify your life, do the things you enjoy and leave the rest, no one cares if you haven’t vacuumed or the laundry isn’t folded. Don’t hide at home and try to push forward. Your not alone and you’ve got this!!
#Spoonie Your not alone and you've got this!! Share on X
If you’d like to contact Sarah, you can find her on Facebook, or catch her via email at nighttiger18@hotmail.com

1 Comment Filed Under: Fibro Warriors Tagged With: interviews

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.

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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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