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You are here: Home / Close to My Heart / Learning to Say “No”

Learning to Say “No”

Last Updated: September 10, 2010

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’ve read over and over again that the women who most often find themselves dealing with Fibromyalgia are “type A” personalities, accomplished woman, over-achievers. I know this applies to me. I was raised to be not only self-sufficient but self-sacrificing; to help others even if it means detriment to yourself. My mother is the epitome of this, and I learned from watching her. That said, I also learned there are limits and I was never as likely to give the shirt off my back as she was. I was more likely to say “no”, although it usually meant a good bit of guilt to do so. In the last year or so I found myself saying “yes” more and more. Not only saying “yes” but volunteering to do things before I was even asked. Why? Because I wanted people to like me, wanted people to appreciate me, wanted people to need me. The funny thing is that they already did. I just never felt like I was “enough”, so I was always trying to do, to give more.

One of the things I learned the fastest when I got sick was that I had to say “no”. At first it was just because I was “sick” and I thought it was a short term thing. I’d still make plans, I’d still volunteer for things, I’d still say “yes”. Then I’d have to cancel the plans or “flake out” on my friends (at least it feels like freaking out). I’ve been sick enough for the last couple of months that I haven’t said “yes” to anything or volunteered to do anything beyond that day, because I know I don’t know how I’ll feel tomorrow. I hope I’ll feel up to something, but maybe I won’t, so it’s better to say “no” than to be the friend who can’t be relied on to follow-through with plans.

Sometimes I wonder why I’ve been afflicted with Fibro, and at times when I stop to think about it I try to think about what I’ve learned in the last 9 months. I know I’ve learned some patience, but more importantly, I’ve learned to say “no”. What I’ve also learned is that those who are really my friends, understand. They understand when I don’t answer the phone, or call them back right away, or when I can’t commit to plans for this weekend. Or when I make plans and I have to cancel at the last minute. I don’t have to be anything more than who or what I am for them to be there for me. I can say “no” and they will still like me. Just as important, I have to say “no” in order to be able to be a friend to them because if I continue to say “yes” when I shouldn’t it will be even longer before I can truely be there for them.

3 Comments Filed Under: Close to My Heart Tagged With: guilt, pacing

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. yngathrrt says

    September 13, 2010 at 3:01 am

    Julie, can you help me follow your blogs, besides FB. I have others that I follow, and get email notifications of any comments I make. Would like to do this with yours as well, but do not get notifications when other give comments, or when you write a new blog. Unless on FB. If I could get notifications, that would be great. You can email me or FB me to explain how to do this.

    Reply
  2. Julie says

    September 11, 2010 at 2:49 am

    They still believe it’s connected to some sort of trauma (accident, illness, etc). For me it followed a year plus battle with TMJ and then I came down with what felt like the flu and has continued from there.

    I think the connection may be that we are A Types used to doing for ourselves then something happens and we have to be dependent. At that point something changes in our brain because of the fight of who we are vs who we want to be.

    I’m still believe to some degree that it’s related to some sort of virus (as they’ve found CFS to be recently).

    Reply
  3. yngathrrt says

    September 10, 2010 at 10:42 pm

    Julie, as always and excellent blog and it speaks words that can be pictures of others that read this. And I agree with so much, almost everything, that you said in this blog. I am an A type as well, and used to be an A PLUS type of personality. This is so hard to explain of how things have changed with me. And I am the worlds worse when it comes to feeling guilt. I have a huge time asking for help from others to, and it has been a downfall for me.

    I meant to tell you that when I came down with Fibro in 1996, I talked to a doctor also of why, and received a pretty interesting bit of news, and not sure if it is true. Back then, they felt that people that suffered from Fibro, had also experienced and accident, or some kind of trauma. I feel off of a horse about 2 months before I started suffering from Fibro. Sometimes I think about that, and wonder if others had some kind of trauma before Fibro set in.
    But, I am like you that Fibro seems to afflict people that are A personality. Those that I have met seem to be. More research. Hugs Katie

    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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