By wendy, on March 10th, 2011%
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Chronic illnesses tend to wreak havoc with family finances. Between the cost of treatment, and the reduction in the ability to work; having an illness like fibromyalgia, bipolar disorder, myalgic encephalitis (chronic fatigue syndrome,) lupus, migraines, or any of the thousands of others out there can destroy a family’s financial security and severely limit the ability to provide traditional healthcare.
My illnesses have put me in the position of not being able to afford the several hundred dollars a month I was spending on medications with my insurance (and with the insurance we have now, the more than $1000 a month they would cost would take pretty much our entire income,) so I’ve had to find other options.
It’s been an interesting journey, and there have been times when I’ve seriously considered just killing myself and getting it over with (mostly during the forced withdrawal from the psychiatric meds I used to be on for my bipolar disorder.) I’ve reached a point now where I’ve found enough other options to manage fairly well, and I’m actually happier without the prescriptions than I was with them. (Even if I hit the lottery tomorrow, I wouldn’t go back to taking all the stuff I used to be on.)
It’s more work than just popping a handful of pills several times a day, but using herbs and aromatherapy to treat my symptoms is also very satisfying. I have much more control of what I’m putting into my body, I’m supporting the natural processes my body uses to heal itself rather than subverting them, and I’m not dealing with multiple side-effects that have to be treated with yet another expensive medication that comes with its own set of side-effects.
Natural treatments do take longer to “kick-in,” and I sometimes deal with slightly higher pain levels than I would if I could just take a heavy-duty pain-killer, but I don’t have to worry about becoming dependent on most of the herbal treatments I use, either. (Which also means that I don’t have to worry about withdrawal symptoms if I switch things around or run out of something.)
There are several herbs that I make certain I always have on hand, and as I promised in part 1, those are the ones I’m going to focus on in this post.
Disclaimer: I am not a doctor, and nothing I say in this post is intended as medical advice. If you find the idea of using herbs in your treatment plan intriguing, be sure to do the research and discuss any changes or additions with your healthcare provider to ensure your safety.
 Making Skullcap Capsules
Skullcap: I use this one for pain reduction (it has actually helped more with my sprained shoulder than the Lortabs the doctor prescribed,) stress reduction, and help sleeping. I try to get it online, from Mountain Rose Herbs, because it’s half the price that I pay at the organic grocery down the street. ($15 a pound, as opposed to $30; so even after I pay for shipping, I save money.)
It works well for headaches (especially tension headaches,) and muscle pain; and in combination with other anti-inflammatory herbs like ginger and turmeric, it also helps with my arthritis/fibromyalgia pain. Continue reading Making My Own “Medicine” – Part 2 »
By wendy, on June 24th, 2010%
Being diagnosed with a chronic illness turns your life upside-down, and it can take you some time to figure out how to deal with it. The sooner you start managing the illness, instead of allowing the illness to manage you; the sooner you’ll start finding ways to live a fulfilling life in spite of it. It can be totally overwhelming at first, but if you take one step at a time, you CAN do it.
The first, and most important, thing you can do is find out everything you possibly can about your illness. Continue reading New to the “Chronic Illness Game”?: How to Survive and Thrive Anyway »
By wendy, on June 18th, 2010%
I have a “Google Alert” set up for CFS, and when I checked today, it led me to an article in the Herts Advertiser titled “Death of “quite fit and well” Harpenden woman a mystery.” The article goes on to state that “Mrs Bellamy had a history of blackouts and had previously been referred to a neurologist for her dizzy spells. But aside from a diagnosis of chronic fatigue syndrome and a prescription for antidepressants, no doctor could find anything wrong with her.”
This is a brilliant example of how misunderstood Chronic Fatigue Syndrome is among the general population, who seem to think that it’s a very minor diagnosis. Continue reading CFS/ME and “Quite Fit and Well” are Mutually Exclusive »
By wendy, on May 20th, 2010%
I think we all hate that question when it’s asked by “normals.” Unless it’s someone you know well, you never know whether to tell the truth (I feel like shit, thanks for asking.) or lie (Fine, how are you?)
Continue reading How are You? How Do You Answer the Hardest Question Ever When You Live with Chronic Illness? »
By wendy, on May 17th, 2010%
My definition
My personal idea of a good day is one where I don’t have to go to work, and I can spend some time just doing things that make me feel better. It does NOT mean that I’m not in pain (I haven’t had a day when the pain levels were below a 4 or 5 on the pain scale in at least 5 years.) It also doesn’t mean I’m not exhausted, or that I can actually remember all the things I need to take care of without lists, notes and reminders from the people around me.
What it does mean is that the pain levels are at a 6 or below, and that I can lay down with the hot pads when I need to, or take a nap. Continue reading What does a "good" day look like to you? »
By wendy, on May 7th, 2010%

In my Sunday post, I promised you complementary/alternative methods you can try for pain and stress control/reduction, so here we go. These methods apply in all of the 4Ps, although they apply in different ways in different stages. Continue reading Learning to Live with Pain – Being Proactive (Part 2) »
By wendy, on May 6th, 2010%
EFT
Does it work? Yes, and no . . . Like anything else, EFT (Emotional Freedom Techniques) has its benefits, but it is definitely not going to make your fibro go away completely. It does, however, help my symptoms and make my fibro easier to live with, so I’ve added it to the resources I use to help me cope. (Is this purely a placebo effect? I don’t really care. If I feel better, or have less pain, it’s worked for me, and I’m happy with that no matter what the mechanism is.)
I downloaded the free EFT manual from http://www.emofree.com and read the information provided, memorizing the steps needed to perform a treatment. The first symptom I tried it on was a migraine, and it worked pretty well. The first treatment eased the pain, Continue reading EFT and Tapping for Fibromyalgia – Do They Work? »
By wendy, on May 5th, 2010%
Jenni has the Learning to Live With Pain Blog Carnival up . It’s a day late, but definitely NOT a dollar short, offering the perspectives of twenty-two amazing babes (and me) on how to live with chronic pain as a permanent unwelcome guest in your life. Check them out, maybe you’ll learn something that will help you or a loved one cope.
**If you are reading this post anywhere other than wendyburnett.wordpress.com it is because it has been stolen. Please click on the link provided to return to the site of origin.
By wendy, on April 27th, 2010%
ChronicBabe is hosting Grand Rounds this week, and they’ve chosen the topic “ladylike.” This post isn’t going to make the deadline (I worked so many hours last week it was all I could do to keep us fed,) so it won’t be in the carnival, but I found the topic interesting, so I decided to write it anyway.
I guess I should probably start with a confession. . . If you used the word “ladylike” to describe me around my friends, they’d most likely laugh in your face. I was a tomboy growing up, and I never really “got” the whole ladylike thing. Continue reading Blowing Your Nose Is Not Ladylike, and Other Truths of Chronic Illness »
By wendy, on April 25th, 2010%
[youtube=http://www.youtube.com/watch?v=SmfxlTXF73w&feature=player_embedded]
A few years ago, my rheumatologist suggested that I try a TENS (Transcutaneous Electrical Nerve Stimulator) for my fibromyalgia pain. She gave me a prescription (be sure to make a copy of the prescription to keep in the case with your TENS in case you need to travel with it,) and I jumped through all the insurance hoops, picking up my TENS unit a few weeks later.
I visited a physical therapist to learn how to use it, and started taking it to work with me every day. I used it constantly for a while, Continue reading Does Using a TENS Unit Ease Fibromyalgia Pain? »

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