Thursday, July 26, 2012

We Need to Fight Fibro Indifference


Indifference refers to the lack of interest or concern from others. Everyone I have spoken with who has Fibromyalgia has suffered not just with the symptoms, but with the people around them not understanding or caring if they understood the true effects of Fibromyalgia.


Fibromyalgia can be a crippling, life altering illness. Fibromyalgia is not a disease. In fact, it is classified as a syndrome because most people with Fibromyalgia have a group of symptoms and characteristics that occur concurrently with the pain. Not everyone with Fibromyalgia has all of the symptoms, but they do have enough of them and have been through enough testing that their medical team believes it is Fibromyalgia.

I wrote an article on ten things that I’ve been personally told at one point or another while riding this Fibromyalgia roller coaster that are cruel or indifferent and generally not helpful, here’s the link if you’re interested TenThings to Never Say to People with Fibromyalgia.

Because Fibromyalgia is an “invisible illness,” meaning there are no obvious physical manifestations, many people who do not have Fibromyalgia simply do not understand the importance of recognizing, not only that Fibromyalgia exists, but also that people with Fibromyalgia need compassion and kindness just like everyone else. 

For some reason, many people believe that because Fibromyalgia isn’t well understood, it must not be real. That could not be further than the truth. Unfortunately, the lack of understanding from others including friends, family, and medical professionals means that another component to the battle of dealing with Fibromyalgia becomes coping with indifference and lack of understanding or kindness.

One of my Fibro friends once told me she wishes she’d gotten Cancer instead of Fibromyalgia. I was stunned by this. Cancer, in my mind, is another difficult and painful illness, but she explained to me. She said that Cancer is respected as a legitimate illness, people with Cancer get support from nearly everyone, and no one would tell a Cancer patient to stop being lazy or they just aren’t trying hard enough to beat it. 

There are known treatments that may or may not work for Cancer, but at least there are set treatments to choose from, instead of having to try everything and deal with nasty side effects that were not known prior to testing and that if they help may only help for limited periods of time. But most of all, people with Cancer aren’t normally treated like they have some odd mental condition that is causing their pain. 

I don’t have Cancer, so I don’t really know if this is true. I suspect Cancer survivors would know better than I, but I do understand what my friend was trying to say. That it would be nice to have something that people generally understood and weren’t indifferent or downright cruel about it.

Unfortunately, we don’t get to choose what illnesses and diseases we end up with in life, all we can do is make the healthiest choices possible and hope for the best. Personally I’d rather not have any illness, but if I have to have one, then I believe that I ended up with Fibromyalgia for a reason. And no, that doesn’t mean I think I deserved this, because no one deserves to go through this. What it does mean is that I believe part of the reason I ended up with Fibromyalgia was because I could end up sharing my experiences with others and hopefully help create more awareness and a safe place for people with Fibromyalgia to learn and share.

If you have a loved one with Fibromyalgia, please don’t be indifferent to their plight. Take a moment and call or visit. Help with something around the house or just hang out and bring some laughter to your loved one.

Whatever you do, please show that you care and that while you may not be able to understand Fibromyalgia completely (really no one does, there is a lot of research going on and hopefully we’ll get some answers soon), you are there to help your loved one when you can and when they are willing.

8 comments:

  1. This breaks my heart because my mom has it, and it makes me be much more compassionate towards the sickness.


    drop by nichollvincent.blogspot.com and say hello!
    xo

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  2. I'm glad it helped you want to be more compassionate about it. It's so tough to deal with and so few people even take the time, like you have, to try to understand. Your mom is lucky to have you!

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  3. A very well written post and it's true; the power of a few uplifting words can be amazing.

    Kind words can be short and easy to speak, but their echos are truly endless.

    ''Love''

    Dusana

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  4. I love the way you worded that. Kind words can be so helpful, but I love the picture that "their echoes are truly endless" conjures for me. Thank you!

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  5. You need to stop expecting people to think about you. Try to get out and see people more unfortunate than you - people living with fear of their lives in wartorn countries, or in poverty.

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  6. Hopefully, as you look around this blog, you will learn a little bit more about Fibromyalgia and the extreme difficulties that it poses for the people who have been diagnosed and their families.


    Many people with FIbromyalgia DO live in poverty because they cannot work due to constant excruciating pain, incomprehensible mental fogginess, and up to 100 other symptoms. Most people with Fibromyalgia experience fear and isolation.


    The goal of this site is to help increase Fibromyalgia Awareness and assist people who are dealing with the issues of Fibromyalgia. To suggest to someone with Fibromyalgia to go out into a war torn country is a bit odd, This blog is about Fibromyalgia, not people who are afraid due to living in war torn countries or focusing on poverty.


    Fibromyalgia is a often debilitating and misunderstood illness that affects millions of people. Many people with Fibromyalgia live in poverty due to being unable to work at all and taking years to get government assistance, if they ever do. People with Fibromyalgia experience a very isolating, horrifying type of fear, which this blog is attempting to alleviate.


    May you enjoy your time on this blog learning more about FIbromyalgia. If you actually begin to truly understand how Fibromyalgia affects millions of people, then you will understand that there is no comparison to people living in war torn countries (other than fear for your life and not being able to live fully) or people in poverty in general (other than the millions of people with Fibromyalgia who do live in poverty -granted poverty in the US is very different than poverty in Ethiopia)


    Also, for the record, I personally do go out in the community when I can and volunteer and help others who are going through many issues, some are actually much worse than poverty.


    I appreciate you taking the time to stop by and learn more about Fibromyalgia and looking around this blog, which is about my PERSONAL experiences with FIbromyalgia (not poverty or wartorn countries).


    I do expect people to think about me, just as I think about them. I also expect people, who I believe are good at heart, to care about other people and appreciate learning more about an illness that affects millions of people in such a horrible way.


    People with Fibromyalgia face a level of pain, frustration, loneliness, and cruelty, that you don't seem to understand yet, I truly hope that whomever in your life who has Fibromyalgia, whether it is you or someone else, learn more about Fibromyalgia.


    If you just accidentally dropped in on a blog for Fibromyalgia then, thanks for stopping by. Good luck in finding whatever it is you are looking for Frankie.

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  7. Emily,
    Your response to Frankie was much more kind and charitable than I could have managed. I honestly thought, when I first read it, that Frankie's remark was an example of what might be found on the list of Ten Things to Never Say to People with Fibromyalgia. It could certainly qualify as number 11 on the list.


    I really appreciated your post on Indifference. I have fibromyalgia and can relate very well to the examples you bring up. Keep on doing what you are doing. You help the rest of us.

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  8. I believe you are correct that the comment could easily and understandably be taken as number 11 of things not to say to people with Fibromyalgia, but the fact that Frankie was on the blog and took the time to leave a response left me believing that it was an educational opportunity.


    I know I was a bit long winded in my response to Frankie, but I wanted to try to educate more without ignoring the fact that I am aware that there are other people in the world in worse shape and better shape than me. The comparisons just aren't very beneficial to anyone, simply because it's comparing apples to oranges and the point of the blog is to share my experiences with Fibromyalgia.
    I am glad the blog is helping you and I will definitely be continuing. :-)
    I think that Fibromyalgia Awareness is extremely important for everyone!

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