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You are here: Home / Conditions / Fibromyalgia / “I Find I Have to Treat My Fibro Patients More Aggressively”

“I Find I Have to Treat My Fibro Patients More Aggressively”

Last Updated: March 1, 2011

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.

I find it interesting that while I constantly hear about how so many Drs don’t believe in Fibro and give patients with Fibro a hard time, I am evidently very lucky when it comes to my Drs.

Today I went to see my Opthamologist, who I just adore. She is so sweet and is one of the only Drs I have that really makes an effort to save her patients money by giving out samples and actually asks about insurance before just handing me a prescription.

My dry eye issues have been getting worse lately so I made an appointment. When I called yesterday they said I could come in at 9:15 this morning. YUCK!

Then at about 8am this morning I got a call telling me that there had been a mix-up and she would be at a different office this morning. If it was too far for me to come she could see me this afternoon. I opted for this afternoon.

She started off by giving me several different samples for drops for different issues, including one that she said helps with Fibro type nerve pain in the eye (why didn’t she give me this 6 months ago!?).

As we discussed all the different drops she made the comment that she has learned she has to treat her patients with Fibro much more aggressively rather than just basing treatment on what she sees in the exam.

I find I have to treat my Fibro patients more aggressively.

 

She said she has like 20-25 Fibro patients now and is learning as she goes. I found this interesting and thoughtful and really rather amazing to hear that Doctor actually said she’s learning as she goes. It seems like most Drs are too egotistical to admit something like this.

Another thing I love about this Dr is that she communicates openly not just with me but with my other Drs. She’s been known to call my Neurologist for me and ask him questions I had.

I followed up with Dr. Schwartz and she agreed to share more thoughts with you on fibromyalgia and eye health. 

Leave a Comment Filed Under: Fibromyalgia, Treatment Tagged With: doctors, dry eyes, eye pain

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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