Showing posts with label chronic fatigue. Show all posts
Showing posts with label chronic fatigue. 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.

Tuesday, August 30, 2011

Blog Award Recieved!

As some of you may have noticed, there is now another image on the side of my blog. It is for being number 35 in their list of "100 Best Sites for Fibromyalgia and Chronic Fatigue Information." This was given to me by a company called VitaSciences. While although it appears they are trying to sell a product, it is also very wonderful that they took the time to make this list to help us find information.


It seems as though this list was compiled back in May in honor of Fibromyalgia Awareness Week. (I always thought it was just a day, but what do I know?) However, I did not get an email about this until just a few days ago.

Here is an excerpt from the page: "In honor of Fibromyalgia Awareness Week, we’ve scoured the web and compiled a list of 100 great websites for people who suffer from Chronic Fatigue Syndrome (CFS), Fibromyalgia and other chronic pain disorders. Below is a conglomeration of personal blogs, government sites, forums and medical pages- some are funny and insightful, some provide lots of great tips on coping with the pain in your life, and some are inspirational…all are gems that we know you will appreciate."

Lastly, here is where you will find the complete list: 100 Best Sites for Fibromyalgia and Chronic Fatigue Information

Sunday, May 22, 2011

Rain, rain, go away...

It's been raining here for the past week and is supposed to for at least another week as well. This rain is killing me. Not only am I in lots of pain, but I also have wicked fatigue, to the point where it's hard to stay awake. I've had it now for a few weeks, but of course the rain is making it even worse.

This having no energy thing is harder for me then the pain. I feel as if I can't do anything at all. Even sitting up on the couch for too long is hard on me. Dan and I really need to be doing some cleaning as we have friends coming over tomorrow night, but where is the energy for that?

I am so tired I just feel like crying. Like all the time. It's really messing with my emotions and it's driving me absolutely crazy. I don't know what to do. I really take Vitamin D3 and a B complex. I take iron as well. I don't know what else to do or try.

Anyone have any advice?

Friday, May 13, 2011

Fibromyalgia Awareness Day 2011

(This was supposed to be posted yesterday, but due to blogger's issues, it couldn't be.)

Here it is again, May 12th. Fibromyalgia Awareness Day. Awareness is SO important because so many people don't know what these illnesses are, or have misconceptions about them. They are NOT psychological, though that is the common belief. Personally, I sometimes wish they were psychological, because then maybe I could just take a pill and see a psychiatrist and be cured. But no, it really isn't that easy. Another reason awareness is so important is because maybe it will help inspire people to do more research, and hopeful
ly even find an effective treatment or cure. Awareness is also important because we have an "invisible illness" and people cannot tell we are sick just by looking at us, which often tends to make people believe that it is not real. Many doctors still don't believe it is real either, because there is no simple test to confirm Fibromyalgia, it is a diagnosis of elimination.

So, what did I do this year? Well, I did a couple of things. First of all, I wore my Fibromyalgia T-Shirt that I had gotten free from Vistaprint. I also participate
d in a balloon release. I only got three balloons, as I couldn't afford many, and also didn't want to do more harm to the environment. I wrote on them. They all said, on one side, "Fibromyalgia Awareness Day, May 12, 2011" and then each had their own writings on them. One was for Felicia Fibro because she wasn't able to do it herself, and her's said: "Hope is my future." I also had one that said "Hope for a cure" and the other one said "I long to be free again" which is a quote from a fantastic song written for awareness. Dan and I took them to the park and set them free. We clipped the strings from them, because I had read that those are the worst part for the environment. It was hard to take pictures of them as they flew away, but we did our best. Other then this adventure, I mostly posted lots of things on facebook and twitter.




Fibromyalgia is truly a debilitating disease. I am currently unable to find a job that my body can handle, and even though I now go to school online, that can be hard as well. The main parts of it are chronic fatigue and chronic pain, but honestly, that is just the beginning. Another big problem I have with it is the fibro fog. Someone can tell me something and I might forget it as soon as 5 minutes later, or sometimes something simple will really confuse me. It is very frustrating. I am only 22 years old and often feel as if I am at least 80. Fibromyalgia has taken many parts of my life away, and I can truly say that my life is not the same as it used to be.

Here is a link that might help you understand some symptoms: http://www.webmd.com/fibromyalgia/understanding-fibromyalgia-symptoms

Do you still have more questions? Ask me, I'm always here and willing to answer.

Also, if you or a loved one suffers from Fibro, what did YOU do for awareness today?

Last, but by no means least, I wanted to share a video I made for Fibromyalgia & CFS/ME Awareness. It looks better on youtube though, so here is the link: Fibromyalgia & CFS/ME Awareness Video.


Thursday, March 31, 2011

Not Quite As Bad As I Thought

So my doctor appointment didn't go quite as bad as I thought, though it still wasn't great by any long stretch of the imagination. I told him that I was not ok with the thought of weight loss surgery, and that I would rather try to lose the weight on my own. He didn't seem too pleased, but he agreed. We have a 6 month goal, and I need to try to get to a certain number by then. If I haven't, he wants me to reconsider the surgery. I told him I would, but I still don't think I'll ever go with it.

So I'm gonna try doing my DDR workouts again. I love that they have the workout mode, because it shows progress that I'm making, plus it's not as boring as most exercising can be. I'm still not excited though, because last time I tried this it made me feel so crappy. But I'm gonna try to start out very slowly and slowly build up.

I still didn't get my referral to the rheumy though. But he didn't necessarily say no. What happened was that he didn't even give me the chance. Once we discussed the weight thing, he pretty much assumed the appointment was over and left. But, his receptionist came up with the idea that I should call the rheumy's office and have them send the paperwork down to the dr. So I did just that. Not sure if it's gonna do any good yet, but we'll see.

Keep your fingers crossed for me!

Thursday, February 17, 2011

Trying To Be Normal

I've been trying to be "normal" lately, as in, doing all the things that other people can do. Dan and I have been doing some crazy cleaning because my mom is coming to visit. It's so exhausting. I've been way over-doing it lately, and seem to be in a flare most of the time. But what am I to do? Things have to get done whether I can do them or not. It doesn't matter. Dan can't do it all himself either. He has joint issues so he's in pain a lot too. We just have to do it, push ourselves, and end up making ourselves worse. It's my attempt at being normal, and I'm failing drastically.

In other news, I have been shaking a lot lately, like my fingers are shaking. I don't know what's up with that. Yesterday it was so bad that I actually felt sick. I ended up eating chocolate and drinking gatorade. I wasn't sure if it was low blood sugar or dehydration, so I tried them both. One or the other, or both, worked. My guess would be dehydration, because that happens to me a lot, plus I've never had trouble with blood sugar. So idk.

I'm back in PT for my knee. I'm seeing a new therapist because the last one was horrible and didn't even believe in fibro. This one believes in it and has experience in it, so I think it'll help. He wants to try this thing called "Instrument Assisted Soft Tissue Mobilization" because my tissue is all stuck and whatnot. Sure, I don't care at this point, just make me better lol.

Ok, I guess that's it for now. Sorry it's been so long since an update, I'll try to do better.

Thursday, November 11, 2010

It's Been Awhile....

It's been awhile since I have written here. Over 2 months in fact. I just haven't had the time and/or energy to do so.

Let's see...what's new. Well, I finished my first term at Kaplan University with straight A's, so I have a 4.0 GPA so far. That is absolutely fantastic news. I never did that well back at USM, it just goes to show how much better this method of online learning really is for me. I'm really glad I made this choice and am finally doing this the right way for me.

On another note, my fatigue has been really bad lately. It's been to the point where I literally can't stay awake for more then a couple of hours without being so tired that I have to go lay down and take a nap. My doctor has prescribed photo-therapy which is like the blue light therapy. Amazingly enough, my insurance actually covered a unit for home use and it's even small enough that I can take it traveling with me. I have used it once so far this afternoon, and so far I'm staying awake. I'm definitely tired, but not so bad that I can't stay awake or anything. I just hope it does help long term, because I definitely need something.

We're going on a cruise in December with Dan's family which I am wicked excited about. We are leaving from NYC and going to Florida and the Bahamas. Just what we need to break up a dreary, cold Maine winter. Plus, I've always wanted to go on a cruise, so I'm very excited about this. I just hope it all goes well, with his family and all. But we shall see I guess.

Well, I guess that's it for now, just wanted to write a quick post since it's been so long.

Friday, August 27, 2010

"Misunderstood" by Mark Emmins (Fibro/CFS Song)

This is an amazing song called "Misunderstood" by Mark Emmins that he wrote for CFS/ME awareness. It applies to Fibro quite well too though. I wanted to share it with all of you, enjoy!

The scars may not show
But the wounds are so deep
Sometimes you never truly see
The pain someone feels
Trapped in the darkness in search of the light
Yet the soul needs to feed
Praying for life to return for me
It's no stranger to you and me
Just want security

It hurts to be touched
And our batteries drained
Confined to the house
Yet our hearts keep on beating
It's not in the mind as our life slips away
Just misunderstood
Just wish for the simple things in life
But you know that's so damn hard
It's so damn hard

Stuck in the darkness but seeking the light
Yet the soul needs to feed
Praying for life to return for me
Loss of hope and loss of friends
I long to be me again
Counted bricks on the walls a million times
Suffering souls
The thing to remember is we're not alone
A simple smile is a giant thing
I long to me again
I long to be free of pain
I long to be free again

It's not in the mind as our life slips away
Just misunderstood
You can't see from outside what's so deep within
Just want security
It's no stranger to you and me