Showing posts with label invisible illness. Show all posts
Showing posts with label invisible illness. Show all posts

Sunday, February 3, 2013

10 Ways To Help Out Your Chronically Ill Friend

This is a fantastic post written by Jenna at http://fibromyalgiaproblems.tumblr.com/ 

1. Don't pull away when they talk about their illness.
Especially if they’re recently diagnosed, they’re not doing it for attention. They’re not doing it for pity, they’re doing it because a diagnosis and an illness are a HUGE thing in a sick person’s life, it’s something to talk about. Just listen, you really don’t have to say anything else. Just be someone they can talk to. 

2.  Do research about their Illness/Illnesses.
Nothing is harder than trying to explain what it’s like dealing with a chronic illness to a healthy person. It’s like explaining color to a blind person. If you know what illness they have, do some research, find out what it is, what symptoms they deal with, and even how other people with the same illness deal with it and describe it. Don’t be afraid to ask questions. 

3. Offer help 
Okay, this one gets complicated. You certainly don’t want to make your ill friend feel bad about not being able to do things. Also, we tend to refuse help. Not always out of pride, but out of fear that people will get tired of helping us or dealing with us.(Like they often do!) So, if you know that something is hard for them(lifting objects, opening doors, opening bottles, carrying groceries) offer help in a way that makes it clear you really want to help, not that you “feel obligated” and also, if your friend says they can handle something, let them. Yes opening bottles hurt, but sometimes we get so frustrated with what we can and can not do that we’re wiling to put up with some pain because we just want to do something for ourselves if we can manage it.

4. Accompany them to Doctors Appointments, or offer to help schedule appointments.
 Scheduling doctors appointments is *such* a hassle with chronic illnesses. Most of us see many doctors, or need to see many doctors, so it can be hard calling all around trying to schedule appointments.
Doctors appointments are also a stressful thing, and it can be nice to have a friend accompany you. It is also hard for many sick people to drive to their own appointments  Your friend may not want you in the exam room with them, but offering to drive them and sit with them in the waiting room could be a *HUGE* help.

5. Understand that they may need to cancel plans last minute, and be okay with rescheduling.
Chronic illnesses are often so unpredictable. We can be doing okay one minute, and in excruciating, unable to move pain the next. Just remember your friend isn’t canceling to stand you up, but because they really need to. Or, remember that sometimes we can’t plan things in the first place. It’s not that we don’t want to go out with friends, we really, really do, but sometimes we’re not healthy enough to have time left over from work or school or doctors appointments or just cooking/cleaning to do anything else.  

6. Go to them, rather than them having to get out. 
Getting out of the house always is hard with a chronic illness. It’s hard to drive, it’s hard to walk far, it’s hard to sit in uncomfortable chairs, it’s hard to be away when we might need our self-care resources we have at home and could need if our health takes a turn for the worse, and it’s hard going places where you don’t know what to expect. Instead of trying to go out to dinner or to a movie or something, go visit them at home and bring take out or cook food, and rent a movie, just have a more quiet night where you can still spend time without your friend having to straining their health. 

7. Try to match their level of humor about their illness.
Some people don’t joke about their illness, so obviously this doesn’t apply so much with them, but a lot of us do. I’m sarcastic ALL the time about little things, I’m constantly joking about my illness, and usually it just weirds my healthy friends out. I still remember the first time a friend make a funny comment about an illness, I take a lot of salt for low blood pressure, and we were watching a documentary talking about how the Mediteranian Sea will eventually be a salt desert, and she said “Jenna! You should live there!” 

8. Don't insist they the new "Miracle Cure."
We try a lot of treatments. Most of them don’t work, or do much at all. We get tired of hearing “Oh my aunt’s sister’s cousin had your illness and drank vinegar-water and now she’s all better! I’m sure it would work for you!” because chances are we’ve tried it and it didn’t work, or we’ve tried something similar and know it won’t work. If you’re doing research or come across a treatment, now and then, it’s okay to say “Have you ever heard of____?” But don’t chastise someone for having a reason not to try that treatment, whatever it is.

9. Don't assume they'll get better.
I know it’s hard to see someone you care about have to be sick all the time, and to know they’re not going to get better. It’s hard for us too. But that’s life, and it just needs to be accepted. You have to accept the fact that there is no cure for most chronic illnesses. That’s why we call them chronic. We don’t have to give up trying to find solutions for certain symptoms, but there aren’t any real “fixes.” In most cases, we just aren’t going to be healthy again, ever.

10. Remember they're still just people.
Sick people always talk about not letting their illness “define them.” It becomes a huge part of your life, obviously. When your friend wants to talk about their illness, let them. When it comes up, be okay with talking about it. But don’t bring it up all the time. We can never “forget” we’re sick, but sometimes it’s nice to act normal and healthy. You have a friend with an illness, but that isn’t all they are, they’re still your friend- a person with so, so much more to them than what they deal with.

aand also: READ THE SPOON THEORY!
It’s a brilliant description of how we have to think and plan our lives around illnesses.

Saturday, July 10, 2010

30 Things About My Invisible Illness You May Not Know

30 Things About My Invisible Illness You May Not Know

1. The illness I live with is:
Fibromyalgia, Chronic Fatigue Syndrome, Asthma, Migraines, Trigeminal Neuralgia, Hypothyroidism, TMJ, Anxiety.

2. I was diagnosed with it in the year:
Migraines 2004, Anxiety 2005, Chronic Fatigue 2007, Fibromyalgia 2008, Trigeminal Neuralgia 2009, Asthma 2009, TMJ 2010, Hypothyroidism 2010.

3. But I had symptoms since:
Some of them for as long as I can remember. I can't remember them all now though.

4. The biggest adjustment I’ve had to make is:
not being able to go out and do things I used to be able, not being able to do the things my friends do, etc.

5. Most people assume:
that it's all in my head, that i'm making it up, that it's not real, etc.

6. The hardest part about mornings are:
Waking up and actually staying awake, getting out of bed, getting ready for the day.

7. My favorite medical TV show is:
Grey's Anatomy and House.

8. A gadget I couldn’t live without is:
My blackberry.

9. The hardest part about nights are:
not being able to sleep, being in pain.

10. Each day I take __ pills & vitamins. (No comments, please)
I take 11 different prescription meds.

11. Regarding alternative treatments I:
go to acupuncture and the chiropractor when I can afford it, I also love reiki but can never afford it.

12. If I had to choose between an invisible illness or visible I would choose:
I'm not sure.

13. Regarding working and career:
I've tried and failed. Looking for something easier on my body.

14. People would be surprised to know:
That I DO NOT like having to rely on other people for things.

15. The hardest thing to accept about my new reality has been:
that it's not going to go away. That this is something I have to accept and live with for the rest of my life. That life is never going to be the same again.

16. Something I never thought I could do with my illness that I did was:
still have at least a bit of a life.

17. The commercials about my illness:
makes me so mad. They act like this medicine cures it and then you'll be fine. WRONG!

18. Something I really miss doing since I was diagnosed is:
going out and doing something with my friends or whoever. I can barely do it now, and when I do, I sure pay for it!

19. It was really hard to have to give up:
my life. Or at least the way it was.

20. A new hobby I have taken up since my diagnosis is:
talking more to my friends and family. Not really a hobby, but its true.

21. If I could have one day of feeling normal again I would:
Hang out with friends and family and have a BLAST!

22. My illness has taught me:
to live life to the fullest, treasure every moment, and help others the best you can. Sometimes all someone needs is a helping hand.

23. Want to know a secret? One thing people say that gets under my skin is:
You just have to (insert something crazy). It's all in your head. (Insert something else here) will cure it.

24. But I love it when people:
when believe I am sick, and treat me that way.

25. My favorite motto, scripture, quote that gets me through tough times is:
I don't know, I have a few.

26. When someone is diagnosed I’d like to tell them:
to do lots of research because doctors DO NOT know it all. And find help and support, it's what will get you through this.

27. Something that has surprised me about living with an illness is:
how hard it is, and yet how it's changed me. And how I've made some amazing friends through the ordeal

28. The nicest thing someone did for me when I wasn’t feeling well was:
just believe me, know I'm not making it up, and helping me in any way possible.

29. I’m involved with Invisible Illness Week because:
I want people to understand that just because someone doesn't look sick, it doesn't mean that they aren't!

30. The fact that you read this list makes me feel:
really good. I hope you understand better now. Thanks.

Wednesday, May 12, 2010

Fibromyalgia Awareness Day

So, today is May 12th, Fibromyalgia Awareness Day. (And as a sidenote, I'm annoyed that I just had to add fibromyalgia to my computer's dictionary.)

I'm not doing much for awareness this year. I have my awareness t-shirt on, but I'm not really leaving the house today. I have no real need to. Last year, I cut up ribbons and made purple ribbons and passed them out to various places. Could of done that this year, but quite frankly, I just don't have the energy.

Ahhh fibro. What to say about it? What to say about a disease that has literally taken my life away? A disease that has made me feel much older then I am? A disease that has changed everything I've ever known?

It has completely and absolutely changed everything for me. I'm 21 years old, and most days I feel like I am at least 80. I have a hard time going out or doing fun things that I used to do, my body just can't handle it. I'm in constant pain, worse pain then I could have ever even imagined before it, and am so exhausted, no matter how much or how little I sleep. My life is not my own anymore, it has been taken over by some kind of horrible monster. A monster who has taken my life away, and left me with this, which sometimes I can't even call a life. Most days it just doesn't feel like it.

But I'm not gonna give up. I can do this. There is hope. I must remember that. Someday, things will get better. Right?

#Fibromyalgia Awareness Day 2010

Sunday, February 28, 2010

A Letter From Fibromyalgia

A LETTER FROM FIBROMYALGIA

Dear Miserable Human Being,

Hi, my name is Fibromyalgia, and I'm an invisible chronic illness. I am now ‘velcroed’ to you for life. Others around you can't see me or hear me, but YOUR body feels me. I can attack you anywhere and anyway I please. I can cause severe pain, or if I am in a good mood, I can just cause you to ache all over.

Remember when you and Energy ran around together and had fun? I took Energy from you and gave you Exhaustion. Just try to have fun now! I also took Good Sleep from you and in its place gave you Fibro Fog (a.k.a.)Brain Fog.

I can make you tremble internally or make you feel cold or hot when everyone else feels normal. Oh yeah, I can make you feel anxious or depressed, too. If you have something planned, or are looking forward to a great day, I can take that away too. You didn't ask for me. I chose you for various reasons: that virus you had that you never quite recovered from, or that car accident, or childbirth, the death of a loved one, or maybe it was those years of abuse and trauma.

Well, anyway, I'm here to stay! I hear you're going to see a doctor who can get rid of me. I'm ‘ROFL’ (rolling on the floor laughing)! Just try! You will have to go to many, many doctors until you find one who can help you effectively. In fact, you'll see many doctors who tell you ‘it’s all in your head’ (or some version of that). If you do find a doctor willing to treat this ‘non-disease’, you will be put on pain pills, sleeping pills, and energy pills. You will be told you are suffering from anxiety or depression, given a TENS unit, told if you just sleep and exercise properly, I will go away. You'll be told to think positively, poked, prodded, and most of all, you will not be taken seriously when you cry to the doctor how debilitating life is for you every single day!


Your family, friends, and coworkers will all listen to you until they just get tired of hearing about how I make you feel, and that I'm a debilitating disease. Some of them will say things like "Oh, you're just having a bad day", or "Well, remember, you cant expect to do the things you used to do 20 years ago," not hearing that you said "20 DAYS ago"! Some will just start talking behind your back, while you slowly feel that you are losing your dignity, trying to make them understand, especially when you are in the middle of a conversation with a ‘normal’ person, and can't remember what you were going to say next!


In closing, you've probably figured out that the ONLY place you will get any real support and understanding in dealing with me is with Other People With Fibromyalgia! They are the only ones that will understand your complaints of unrelenting pain, insomnia, fibro fog, the inability to perform the everyday tasks that ‘normal people’ take for granted.
Remember, I'm stuck to you like Velcro – and I expect we'll be together for the rest of your life.

Have a nice day!! (ROFL),

Fibromyalgia

Friday, October 23, 2009

Unwell - Matchbox 20

[This song was not written about someone with a chronic illness, but if you look at it from that point of view, it definitely makes alot of sense. Or maybe that's just me.]

All day staring at the ceiling
Making friends with shadows on my wall
All night hearing voices telling me
That I should get some sleep
Because tomorrow might be good for something

Hold on
Feeling like I'm headed for a breakdown
And I don't know why

But I'm not crazy, I'm just a little unwell
I know right now you can't tell
But stay awhile and maybe then you'll see
A different side of me
I'm not crazy, I'm just a little impaired
I know right now you don't care
But soon enough you're gonna think of me
And how I used to be...me

I'm talking to myself in public
Dodging glances on the train
And I know, I know they've all been talking about me
I can hear them whisper
And it makes me think there must be something wrong with me
Out of all the hours thinking
Somehow I've lost my mind

But I'm not crazy, I'm just a little unwell
I know right now you can't tell
But stay awhile and maybe then you'll see
A different side of me
I'm not crazy, I'm just a little impaired
I know right now you don't care
But soon enough you're gonna think of me
And how I used to be

I've been talking in my sleep
Pretty soon they'll come to get me
Yeah, they're taking me away

But I'm not crazy, I'm just a little unwell
I know right now you can't tell
But stay awhile and maybe then you'll see
A different side of me
I'm not crazy, I'm just a little impaired
I know right now you don't care
But soon enough you're gonna think of me
And how I used to be

Yeah, how I used to be
How I used to be
Well, I'm just a little unwell
How I used to be
How I used to be
I'm just a little unwell

Saturday, September 5, 2009

When You See Me - Fibro Poem

WHEN YOU SEE ME
written May 2003
When you see me on a "good day"
I may look as if nothing's wrong,
But I, myself, am very aware
That the energy won't last long.
You may think that I am lazy,
Or I just don't like to try,
Or maybe I am just depressed,
When sometimes you see me cry.
You may not understand me,
It's not easy to explain,
The struggles that I so often endure,
As I live each day in pain.
People may offer their opinions,
Thinking that I just need some advise,
Yet they don't really comprehend,
Although they are trying to be nice.
What for some may be so easy,
Is almost impossible to me,
But because I may look healthy,
Many around me fail to see.
Perhaps it seems that I'm sloppy,
If I would only take more pride,
It's sad that many don't stop to see,
The person who is inside.
Planning things is so hard to do,
With each day uncertain fate,
The best that I can do is try,
And oftentimes I have to wait.
Life can be so stressful,
Even when you have your health,
Many people cannot even imagine,
Giving up their dreams and wealth.
While some people may worry,
How to fit everything into each day,
Others of us must struggle,
To even find a way.
So often misunderstood,
Some say that is must be "in my head,"
Yet there are days that it takes all I have
To even get out of bed.
You'd think that if one is weary,
Then why not just take a nap,
But the fatigue at times is so severe,
That nothing seems to help.
I guess it would be a better thing,
If there were a little more support,
Everyone longs for acceptance and love,
As they keep their life in sort.
If I could make the world aware,
Help them to see things in a new light,
Be careful on what they base their view,
That they may receive a new insight.
Then maybe when someone else comes along,
Who is going through something unknown,
They may not feel so hopeless and scared,
And will know that they're not alone.
Whether it be a terminal thing,
Or something chronic with no known cure,
There are many processes that will be faced
In this we can rest assured.
The grieving over loss is hard,
Whatever the loss may be.
What may be just a bump for you,
Could seem like a mountain to me.
For I faithfully trust in God above,
And no matter what the future may bring,
I know that He is holding my hand,
And He's in control of EVERYTHING.