Loneliness is the Most Terrible Poverty
Posted by Purple Law Lady
I’ll admit that sometimes I like to just hide alone in my little house and be by myself – because (beyond the physical) living with the emotional pain of trying to cope with FM can be exhausting. And, sometimes, I don’t want to put on my happy face; I just want to sit, in silence, and brood.
But whether you’re all alone, by yourself like me, or all alone and surrounded by people who don’t understand, living with FM can feel total isolating.
There are plausible reasons why living with FM makes it seem like you’re living on the peripheral of life:
- An Invisible Condition. FM is an intensely painful experience for us, but it is invisible to those (especially those who aren’t really looking) around you.
- Trauma. FM, whether set off by a traumatic event or not, is a trauma in itself. It is like a permanent fight-or-flight setting, and when your whole system is set to trauma response, it’s hard to invest in relationships.
- Altered sense of self. Chronic pain can change the way we relate to ourselves. If the relationship with ourselves is disrupted, you’ll see ripple effects in all your other relationships.
- Other people’s reactions. Living with FM often means becoming accustomed to the people around you telling you that your condition is “all in your head” and that you should “snap out of it.” But you know what you feel is real, and being misunderstood and judged isn’t conducive to happy relationships.
- Practical barriers. Pain, fatigue, and related problems such as sleeplessness and mood changes can make it difficult to show up at social events or even work up the energy for a phone call. It makes it very difficult to do the things you want to do. You can never make plans, as you never know how you are going to feel from day to day. These barriers cause isolation and may even lead to depression.
Connecting with supportive people, although not always easy to find, can help us overcome these emotional side effects.
The Ultimate Relationship Dream List
- Working with a doctor who understands fibromyalgia and is keeping up with cutting-edge research should lead to effective treatment approaches — perhaps medication, lifestyle changes, or alternative therapies such as acupuncture.
- You want a variety of relationships, and spending time with others who have FM could ease some of your isolation. There may not be others within your physical proximity but you can establish cyber-relationships by joining on-line support groups that meet your needs. My Facebook page may not be your sort of thing, but at the bottom of this page is a list of other support groups that you might want to explore.
- Don’t engage with the people who say FM is NOT real – although you can’t cut off your family, you can limit the time you spend with those who refuse to acknowledge what you’re going through.
- Whether it stems from living with FM or has another cause, depression is a common coexisting condition. Depression treatment or stress-coping skills should be part of your treatment plan and will help ease loneliness as part of the healing process.
- Don’t forget to give yourself time to see results – forming relationships takes time. As your emotional distress eases and we find ways to manage our stressful relationships, hopefully we will start to feel less isolated.
- And, lastly, believing you will be trapped forever in an incurable, painful condition can be a self-fulfilling prophecy. So if that’s your mind-set, it’s time to start building a support system of doctors, nurses, friends, and family. This network will help you cope with and manage your fibromyalgia symptoms more effectively so you can get back to the life you deserve.
About Purple Law Lady
Wow! I was 40 before I heard about Fibromyalgia. After spending 6 years working (in the 'real' world) and studying to get my law degree, half of which I suffered (literally) with depression, I was able to 'practice' law for one whole month before the debilitating purple wave took over my life - FIBROMYALGIA! Unlike many, I have NOT learned to manage this condition so I am not working and I spend alot of time on my couch. So I've decided to share this time with you (who may be real people or may just be the 'ether').Posted on June 28, 2012, in Depression, Fibromyalgia and tagged Alternate Therapies, bệnh đau cơ xơ, chronic illness, chronic pain, Conditions and Diseases, 線維筋痛, 纤维肌痛, Depression, Facebook, Fibromyalgia, Fibromyalgie, Health, illness, isolation, La fibromyalgie, pain, Relationships, Social Media, Support group, فيبروميالغيا, פיברומיאלגיה. Bookmark the permalink. 7 Comments.










I just wanted to thank you for writing this – I hate that you have to live this, too, but it helps to know that we are not alone & that we have someone who understands us… Each other! God bless you, my friend!
Your words are the exact thoughts I have had
The last few days. Coming off of an almost
Unbearable 5 day flareup!!! You are right,
I am so weak and exhausted I can barely lift
My arms. Correct on not being able to make
Plans. Correct on not feeling like talking on
The phone and I just wish my family really
Understood. My daughter-in-law told me I
Just needed to relax!!!! No clue of what we
Go through. Thank you for being here for us.
Powerful words pretty lady, I only hope that you find some comfort for your self by sharing all it is that “we” endure and you are so right about the self fulfilling prophecy. My motto is: not to ask for easy days but to have the strength to conquer the bad ones. I have been documented Crazy too many times to count and yet I am still hear fighting just for the right to live my life with out constant misery by any means possible. Thanks to you and yours I No longer feel isolated and I am so grateful for a soft place to land when times are at the worst. I will also be here for you if at all possible I hope you now consider me part of your team there is definitely strength in numbers. And prizes are always good I just cut a bunch of wild flowers enjoying natures beauty helps me experience joy. Take good care until next time sending you warm healing hugs Lori
You have made many points that extend beyond FM. It is definitely a difficult disease to live with and if you could be better you would. It’s unfortunate that so many don’t understand or even try to understand what all the FM sufferers endure. I am going to reblog this on my site. It overlaps with so many features of brain injury and of course chronic illnesses of all types. Great writing!
Wow Miss this is the best post you have ever done in my eyes and they are filled with tears because I wish for those things in my life! Having just moved away from my support system…I am finding it so very difficult to locate even one of understanding doctor. Really if I did not have the support of my online FM support groups I would be completely alone with this fight!
Bless you for writing this. Brought tears to my eyes.
The points you make fit so much with how I feel, and I don’t have FM. I do have other chronic illnesses, the main two are Meniere’s Disease and chronic Migraine disease. Both invisible illnesses.
Thank you for writing this.
My only real friends now are on line. I miss having real friends. I do have a wonderful husband, but he can’t fulfill all the holes that are left in my heart by all the friends who have faded away. However, he is wonderful. I don’t know where I’d be without him.
again, thank you for this post.
wendy