The first, Long-Term Opioid Therapy – What Are the Effects?, brings us the results of Dr. Forest Tennant's ground-breaking study. He evaluated 24 chronic pain patients from 30 to 79 years old who had been using opioids for 10 to 35 years, and "concluded that the significant improvements in quality of life and physical functioning from opioid therapy are so positive they outweigh any negative complications, which can be easily managed."

Almost all of the patients (22 of 24) said their pain had permanently decreased over time. And the vast majority (20 of 24) felt their opioids still provided the same relief as when they started treatment. All of the patients reported one or more functions or activities they can do now that they couldn't do prior to beginning opioid therapy (i.e., get out of bed everyday, take walks, shop or visit friends).

The article details the patients' diagnoses and gives further information, and I encourage you to read the rest of it. While the study was small and obviously needs to be repeated with a larger group, this is marvelous news, and I for one and very grateful for Dr. Tennant's work and the participation of his subjects.

I have to say that I find HealthCentral's sites to be generaly decent, but the Chronic Pain Connection is outstanding. I encourage you to visit and subscribe to the newsletter.

Next, in One Patient’s Experience with Savella for Fibromyalgia, Richards brings us detailed feedback from one of her contacts, Brenda, who has been taking the new drug for seven weeks. Many of us have heard of Savella, but so few have had an opportunity to try it or know anyone who have that this article is very helpful in making a decision as to whether or not to ask our physicians for it. After reading about Brenda’s advice regarding insurance experiences, dealing with side effects, and positive results, I for one will be talking to my neurologist about a trial pack.

So like an HPV diagnosis in someone would almost guarantee that others would know the person’s potential morals or lack there of, and HIV almost always denotes a gay man, a diagnosis of fibromyalgia could potentially indicate a woman who has aborted a child. Just a thought.

Gosh - so all those males who have fibromyalgia were actually born as women, and had abortions before they had sex changes and developed FMS? Everybody who is HIV+ because of blood transfusions or other issues is a gay man?

I’ve never even considered having an abortion. My child certainly hasn’t had one, and she developed FMS when she was nine years old!

I did comment at the blogger’s site, giving her information on all the proof that FMS does exist and that our pain is real. I don’t believe she’ll ever approve the comment, because she doesn’t care about the truth — she just wants to spread her nasty propaganda.

Being in pain all the time can certainly lead to depression. That’s just logical. There are, however, people who have fibromyalgia who are not clinically depressed. Depression can also manifest as physical pain, but it is does not meet the criteria for fibromyalgia.

I was treated for depression for years before I developed FMS, though, and I truly believe that if I’d gotten proper treatment for mental health issues in my childhood (post-traumatic stress disorder and all the complications it brought, including major depressive disorder) I probably wouldn’t have developed FMS.

I never have trouble distinguishing between the two, or between either of them and CFS/ME, which I also have. They’re all quite different.

With FMS, the pain causes fatigue, and together they can (but don’t always) have an affect on your emotions. You may feel like doing something, but your body absolutely will not cooperate. There have been times when I’ve been feeling great, gone out to do something I was SO looking forward to — and nearly collapsed in the middle of everything when my body said, “All right, that’s it, no more. Done. Where’s the bed?” (We’ve joked that if I ever manage to get a scooter or electric wheelchair, it will have to have a remote control feature so that Sam can steer me on home when I’ve passed out.)

But serious clinical depression…it doesn’t matter whether you’ve got the physical energy or not. Logic doesn’t matter. Knowing that you’d feel better for having a nice, hot shower is utterly irrelevant. The fact that the telephone ringing is contributing to your headache, and you could make it stop by merely lifting up your arm up pushing a button, is irrelevant, because lifting your arm would take too much damned effort. Yes, somewhere, on some level, you may know that you’ll lose yet more function for not getting up and doing your exercises, but it’s less important than staring at the ceiling, or the pillow, or whatever is in front of your face right now. Not that you really make any kind of conscious value judgment or anything, but the staring has inertia going for it. Even if nothing IS hurting, even if you have all the energy in the world and you could do anything you just don’t care.

Remember that, the next time you hear someone claiming that FMS and depression are the same.

I’m pleased with it. There are very few, mostly immaterial inaccuracies.

She also interviewed Sam, since the topic was “fibromyalgia and intimacy.” He’s so wonderful!

I hope all of you had a great day