Showing posts with label pain. Show all posts
Showing posts with label pain. 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.

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

Sunday, August 30, 2009

Pain....and other things...

Ok, so I suppose its time for a new update, since it's been awhile.

Last week was pretty much same 'ol same 'ol. I ended up going to First Care at Maine Med for my knee on Wednesday night. They took x-rays and such and couldn't find anything. The doctor then did an exam, and he said that he thought I had bruised the bone. They wrapped it in an ace bandage, told me it would be 2-3 days til it felt better, and then sent me on my way. Oh man was I in pain.

We got notice from Dan's insurance company that his car was totalled. Not good news at all. So on Thursday we went up to Richmond to get everything out of it, which was actually alot of stuff. I didn't even realize we had that much stuff in his car! And man was that painful on my knee doing all of that work. But Dan was good as usual and didn't make me do more then I felt I could handle. Unfortunately, what I "thought I could handle" was more then what I really could.

We then went to South China for a couple of days since we were right there anyways. We stayed until Saturday and then came back to Portland. During which, my knee was still killing me, and the ace bandage wasn't helping any....in fact I feel like it was making it worse because it was cutting into the skin. (And I didn't even have it that tight!)

This morning I woke up and my knee hurt even WORSE. And it had been 4 days. I knew something wasn't right, so I decided to go back and see another doctor, because I just wasn't ok. So we went to Mercy's FirstCare and saw a doctor. She said the other doctor WAS right, that is a bruised bone, but that it def wouldn't heal within 2-3 days. She said it may be a few weeks. She then gave me a knee immobilizer to use and crutches to use in extreme circumstances. I'm glad that it was nothing serious, and that this doctor had a clue. But man oh man, the pain is so extreme and I don't have anything for it. It's worse then my fibro pain I think. But then again it's hard to tell, because it is probably both acting up.

Sooo on Wednesday I have a doctor appointment. After talking to some people, I have decided that I am SO going to put my foot down and demand a referral to a pain specialist. I don't care that he thinks I don't need to see one. I have been in so much pain for so long now, and none of the fibro meds seem to be helping, so I NEED to do something. And as much as I would hate to do so, if he doesn't oblige I will start looking for another doctor, although like I said, I would hate it if it came down to that.

Well, I guess thats it for now. I hope everyone is doing well! <3

Tuesday, August 25, 2009

Life continued....

So let's see, what is new in my life?

Well, the heat nearly killed me. I felt so sick, and I passed out numerous times. Luckily, it rained this weekend and that cooled me down some. One night, Dan and I went for a walk in the rain in the park. It was amazing, and it made me feel so much better.

I went to the neurologist on Monday, and that wasn't a huge help. But seriously, why am I surprised? He did up my Lyrica though...I'm now on 225mg twice a day. I wonder if it will help? I feel like nothing ever does. I've been in so much pain lately and so tired. My knee has still been bothering me. I fell on it like 2 weeks ago, and it still bothers me alot. I don't know if I actually did some sort of damage or not, but it def feels like it.

Umm. Mike and Shawn came to visit today, and that was nice. Our friendships have been strained numerous times, but its still there, and thats always a good thing. I really do miss them on occasion, so it was really nice to see them and catch up and everything. And reminscing about old times. As much as I love the present, sometimes I really do miss the past. Sometimes I really wish I could go back. But I do love the present. Ah. It's hard to explain.

I am going to take some classes at SMCC this semester. I am taking some online classes because attendance is really hurting my grades, and with online classes I can do my work even if I am sick in bed. So I think its a good plan. Because I really don't want to give up school, no matter how hard it really is most of the time.

Ok, thats it for now. <3

Saturday, August 22, 2009

Herbs That Provide Natural Pain Relief

Herbs That Provide Natural Pain Relief

By: Jacob Teitelbaum

Many natural therapies can be very helpful for pain. My three favorite pain relieving herbals are willow bark, boswellia, and tart cherry. All three of these can be found in combination in the End Fatigue Pain Formula by Integrative Therapeutics. Begin with 2-4 tabs 2-3 times a day as needed until maximum benefit is achieved (approximately 4-6 weeks) and then you can use the lowest effective dose. Let's look at these three herbals.

Willow bark is the original source of aspirin, but when used as the entire herb it has been found to be much safer and quite effective. The active ingredient is salicin, and willow bark has been shown to be effective in both osteoarthritis and back pain. People who are severely allergic to aspirin (e.g., aspirin induced asthma or anaphylaxes — which is very unusual) should not use willow bark. Like aspirin and Celebrex, it acts as a COX (Cyclooxygenase enzyme) inhibitor, decreasing inflammation. There are clearly a combination of other factors in willow bark that markedly enhance its effectiveness and safety—which can be a major benefit over aspirin and NSAIDs (e.g., Motrin®) which cause an enormous amount of gastritis and ulcer bleeding, to the point of killing 15,000-20,000 Americans yearly! The studies on willow bark are quite consistent in their effectiveness in reducing pain. Let's look at some of the research.

In one study, 210 patients with severe chronic low back pain were randomly assigned to receive an oral willow bark extract with either 120 mg (low dose) or 240 mg (high dose) of salicin, or placebo, in a 4-week blinded trial. In the last week of treatment, 39 still showing benefit at the end of 12 months despite having stopped the treatment. That lipoic acid helps in several kinds of neuropathies suggest that it is worth trying in others as well, as it is quite benign and not very expensive.

SAM-e is a nutrient produced from trimethylglycine (betaine) in combination with multiple nutrients including B vitamins, folate, and inositol. It was initially tested and found to be effective in treating depression. Researchers also noted as an aside that it improved patients' arthritis as effectively as anti-inflammatory medications (NSAIDS). A number of studies were done including one which gave 600 mg a day for 2 weeks followed by 400 mg daily for 2 years. Pain and stiffness decreased within one week and the improvement continued throughout the two-year trial. A study which reviewed seven other studies was inconclusive. A major problem with SAM-e is that it is not stable and breaks down easily, with many products not really delivering what they claim. In addition, it is quite expensive. An alternative that I prefer is to use the nutrients needed to make SAM-e in your body. Doing this in several patients (using the nutrients found in the Energy Revitalization System vitamin powder) resulted in increased blood levels of SAM-e similar to those found by taking 400-800 milligrams daily.

What Else Should I Keep in Mind for Pain?

As noted above, pain is the body's way of trying to get your attention. In addition to asking for nutritional support, pain also can be a sign that the patient needs 8+ hours of deep sleep a night, hormonal support, and to treat any underlying infections (especially yeast, parasites, and sinusitis). These and a host of other natural remedies (and how to tailor them to specific situations) are discussed at length in my book Pain Free 1-2-3! and previous articles. See our SHINE Treatment Protocol for more information on over 200 available treatments (by category), including dosing and other patient instructions. This will give you detailed information on the different therapies available for each problem and how to use them.

With so many safe and effective natural remedies available for pain, it is no longer necessary for over 50 million Americans to be in chronic pain, and tens of thousands to die each year from NSAIDs and other pain medications! Isn't it time for you to be Pain Free?

Sunday, August 16, 2009

An open letter to anyone who has a fibromyalgia patient in his or her life.

An open letter to anyone who has a fibromyalgia patient in his or her life.

By Karen Lee Richards

If you are reading this, someone close to you lives with and suffers from fibromyalgia (FM). Since FM is invisible, many find it hard to believe that it is a real illness or that anyone could really hurt that much all the time. Unfortunately, this is one of the main reasons that fibromyalgia is so often misunderstood, misdiagnosed and not properly treated.

Fibromyalgia is a central nervous system disorder that has three primary components: pain, fatigue and sleep problems. (1) Pain – The pain may vary in intensity and location, but it is present most, if not all, of the time. (2) Fatigue – The fatigue is not like the tiredness you might feel after working too hard or overdoing it on a sports field. It's a pervasive, all-encompassing exhaustion – like someone pulled the plug on your energy source. (3) Sleep – The person with FM usually has difficulty sleeping. And even when they do finally sleep, they never reach that deep REM stage of sleep where the body refreshes and restores itself.

The root cause of fibromyalgia remains a mystery, however, it is usually triggered by some kind of trauma to the body, such as an injury or illness. In some cases, it can also be triggered by a severe emotional trauma. Regardless the source, FM devastates the life it touches. Unrelenting pain and fatigue reduces a person's ability to concentrate, perform daily tasks, work, socialize, exercise and sleep. The more severe the symptoms, the more incapacitating it can be. Fibromyalgia often leads to depression, isolation and loss of self-esteem. Sadly, people whose FM is poorly controlled may also be at increased risk for suicide.

There are four main things someone with fibromyalgia needs you to understand:

1. What they are feeling and experiencing.

If you have a difficult time imagining what it must be like to live with the pain of fibromyalgia, I'd like to challenge you to try an experiment. Take a wooden clothespin – the kind with the spring that works by pinching one end together and clamping the other end to the clothesline – only instead of attaching it to a clothesline, clamp it to the end of one of your fingers. Now go about your business and see how long you can leave it on. While you still have the clothespin attached to your finger, try to imagine how it would feel if you knew you couldn't take it off when the pain got to be too much. What would it be like to have that non-stop pain all over your body? Now think about what it would feel like to have the flu at the same time – the kind of flu where every muscle in your body aches and it takes every ounce of energy you can muster just to drag yourself out of bed. Finally, imagine that the pain and fatigue doesn't just continue for a day, or a week, or even a month, but goes on for year after year with little hope that it will end. If you can imagine that, then you have a small inkling of what your loved one lives with each and every day.

2. What they are not.

Fibromyalgia is not a psychological disorder – it is an all too real physical illness. Those who have it are not hypochondriacs; nor are they lazy, overly sensitive or just trying to get attention. And they are not simply depressed. Although depression may or may not accompany FM, it is not the cause of it. The percentage of people with FM who also have depression is no greater than for any other chronic illness.

3. Every fibromyaglia patient is different.

The differences in FM patients exist on a couple of levels. One is the severity of their symptoms. While one patient may be able to continue working, another may be severely disabled and in some cases, even confined to a wheelchair. Just because you may know someone else with FM who is functioning fairly well doesn't mean your loved one is faking or not trying hard enough. It simply means they have a more severe case.

Another big difference is how various treatments options work. What helps one person with FM doesn't necessarily help another. Also, people with FM tend to have a lot of sensitivities to medications, so it often takes much trial and error to find something that will help. We find that what works best for most FM patients is some combination of medication, gentle exercise, lifestyle changes, and often some kind of complementary treatment like massage therapy, acupuncture, supplements, etc. Unfortunately, it can take a long time to find that ideal combination.

4. What you can do.

The main thing your friend or family member needs from you is your understanding, support and encouragement. They know you can't take their pain away. They just want you to listen without judging them and let them know you care. Often people with fibromyalgia have told me that the emotional pain of having loved ones question the validity of their illness or accuse them of just being lazy is, in many ways, worse than the physical pain they have to deal with. They already struggle with feelings of guilt because sometimes they can't “be there” for family and friends as much as they'd like to be. Try to reassure them that you care about them for who they are, not just what they can physically do for you.

If you'd like to know some other ways you can help, there's a very nice and inexpensive little book that is chock-full of suggestions. Read my review of Beyond Casseroles: 505 Ways to Encourage a Chronically Ill Friend for a sampling of its contents.

Finally, if you'd like to learn more about FM, please check out our Fibromyalgia page at ChronicPainConnection.com and feel free to ask questions.

Best regards,

Karen Lee Richards

ChronicPainConnection Expert

Monday, August 10, 2009

So I'm bad at this already...

So it looks as though I am bad at keeping up with this blog already, as I have missed a few days. But I'm really really really gonna try with this one, so here's another post.

I've been sick over the weekend. At first I thought it was just some cold sort of thing, because thats what the symptoms were. But then on Sunday I seemed to have a fever. According to Dan I also passed out for like 20 minutes. WTF? Why did I do that? I guess my body just couldn't handle it anymore. I seem to be feeling better in that sense today though, so thats always a plus. I'm having a high pain day though, which isn't any fun whatsoever. I really wish I had some pain meds for it. I mean, don't get me wrong, I am scared of them because I really don't want to become addicted, but I can't deal with this pain either. It's making me pretty much bedridden, and I hate that more then anything. Next time I see Dr. Winn, I am putting my foot down and demanding he does a referral for a pain specialist. I just can't take this anymore.

Nice rant there, eh? I feel like so many of my blog posts have been rants, and in some ways I hate that, but seriously, where else am I supposed to bitch and moan? Well, ok, I do it on Twitter too. ;)

Other then pain, things seem to be ok. Dan and I are doing wonderfully. He always takes care of me and I don't know what I would do without him. I'm so lucky to have him. I couldn't ask for anyone better, and I couldn't ask for someone more helpful or caring. Even as I write this, he is making dinner. :)

Had a chiropractor appointment today, and things feel better then they did. I can definitely feel that my body is back in alignment where it should be, and I feel more balanced and even. I love how it feels right after the appointment, I just wish it would last longer and do more for the pain.

I have a job interview for Thursday. It's for a part time sales associate job. I'm not even sure if I can handle it, but all I know is that we desperately need the money, and if we don't do something soon we're gonna be in bigggg trouble. So I'm gonna try this. I really hope I get the job, and I really hope that I will be able to keep it.

Well, that's it for now I guess, time for some yummy dinner that Dan made. :)



Friday, August 7, 2009

Just not feeling it....

So, this morning I woke up early, (for me), and headed to Yarmouth for my Reiki session. It was amazing as always, and again, as usual, I felt so much better. I really can't believe how much Reiki really does do for me. Anyways, I bought some isotonix mixes too, which are natural supplements to help your body. I'm glad I did it, because we all know that my body can use any help it can get, but oh man, I shouldn't of because I can't afford it at all. I wrote a check for 135 dollars and some odd cents, and there was definitely not that much money in my bank account. Why did I do such a thing? Simple. Because I want to feel better. I'm sick and tired of feeling like shit all the time. I'm sick of not really "living." (And yes, the money is now in my account, no worries.)

But seriously. I'm not sure how much more of this I can take. It sucks being only 20 years old and not being able to do things people my age do. It sucks being bedridden some days and not have a life. I'm sick and tired of being sick and tired. I hate not feeling like myself anymore and not being able to do things I used to be able. I'm only 2o years old and sometimes I feel like my life is over. This just isn't fair. I know life isn't fair, but I feel like I really can't handle this anymore. It's just really started to get me depressed. I just wish, more then anything, that I could feel better, and at least feel a bit more back to normal...that would be so nice.

So other then that rant, I'm doing alright. I'm just sorta having a down sort of night.

Thursday, August 6, 2009

Fibromyalgia

Fibromyalgia-
The name is so complicated
And so is the disease.
Chronic pain, chronic fatigue,
Those are just the beginning.
Do you know what it feels like
To wake up and feel so much older then you are?
Do you know what it feels like
To not be able to do things everyone else does?
Do you know what it feels like
To not be able to do things you once used to?
Do you know what it feels like
To have the littlest things
Wear you out completely?
Do you know what it feels like
To have no one believe you are sick?
These are all things
That I feel every day.
My body is not my own anymore,
Something horrible has taken it over.
Can I ever win it back again?
Will I ever feel ok?
Will I ever feel normal again?