Showing posts with label fibromyalgia. Show all posts
Showing posts with label fibromyalgia. Show all posts

Monday, December 3, 2012

The End of Chronic Pain

For 20 years now I've had unexplained chronic pain in my upper body. It's been there when the autoimmune stuff is flared up, and it's been there when it's not, even when all my "lupus tests" are negative.

(Note: there's really no such thing as a specific "lupus test," but there are tests that show antibodies that are loosely linked to lupus and used as one part of deciding on a lupus diagnosis. You can have lupus even though your tests appear normal, and you can have abnormal tests and not have lupus... so they aren't the be-all and end-all for diagnosis. However, in my case, when I've been very sick, my tests were very abnormal- so, for me, a bad test just confirmed what we already knew- the lupus/autoimmune stuff was in high gear.)

But let's get back to the issue at hand: chronic pain that has no explanation.
I've tried everything under the sun to eliminate this pain.

- Chiropractic. Went 3 days a week for a month, and the pain always returned within a few hours. He told me my neck was out of alignment, but the adjustments only made me feel better for such a short period of time.

- Acupuncture. helpful for other things, but not so much the shoulder pain. Still, no real explanation for the pain.

- "regular" medicine (rhuematologists, neurologists, GP, etc). Here I got drugs (advil, Aleve, aspirin, Saulsalate, percocet, vicodin) and pain creams and patches (biofreeze, icy hot, arnica, salonpas) (I'm sure I'm forgetting some- I've been at this for 20 years...). Sometimes I've taken so much percocet it made me hypothermic (because of all the tylenol in it), and the pain was... still there. And not to mention the constipation. Oh, I just mentioned it, didn't I? And of course, no closer to knowing why I was in pain. I just used the drugs to help manage it.

- a TENS unit (electrical stimulation). I also used this for much longer periods than suggested. Gave some relief, but only while it was on. And still no explanation for the pain.

- Heating pads and ice packs.

- Massage. this actually really helped- if i could get massage every DAY! Maybe if I were super rich and famous... Which led me to think ... muscle tension is behind this. But why so much tension?

-Physical therapy. Did this for 6 months. Thought I had found the "source" of pain- tendinitis in my right arm. So we worked on that for 6 months, 2-3 times a week. Every session, I got heat for 10 minutes, then massage for 10 minutes, then exercise for 15-20 minutes, then ice for 10 minutes. Sometimes I couldn't make it to an appointment because I was out of town, but I would continue to do my exercises at home/ on the road. But the pain would return. So... the exercises were not eliminating the pain. And I would heat and ice myself. Not enough. Clearly it was the frequent massage keeping things under control. That's what I learned from 6 months in PT. Something I kinda already knew- massage helps me more than anything. Unfortunately, the amount of massage it takes for me to be pain-free (3 times a week) is more than I have time or money for. But I did still want to get some massage, even if I can't go 3 times a week.

Sidebar: having the diagnosis "tendinitis" still doesn't give an explanation as to where the pain came from. It's just another label for my problems, but it doesn't tell me WHY I'm in pain. I was also told I had "adhesions," those things I call "crunchies" in my shoulder and back muscles, that feel like big lumps of salt that I can break up and dissolve if I work at it, or have someone else work at it (massage). OK, I have a new word: adhesions. But WHY do I have adhesions? It's kind of that circular logic: Why do I feel like crap? Because you're you're sick. Why am I sick? Because that's the label we give you when you feel like crap. Wow, thanks. What do I owe you for this bit of wisdom?

While my "why?" remained unanswered, I at least had a "how"- as in, how to get some relief: massage. I made numerous attempts to find a decent massage therapist (FYI, in New Jersey, you don't have to be licensed! Any schmo can put up a sign and sell massages!). Massage has become very popular around here as a business with people who just arrived here from China and the only English they know is "30 or 60 minute?" and "cash or credit card?" I had some AWFUL massages. One was so pointy, I think all she used were her thumbs. It felt like I was being walked on by a 30-pound cat wearing high heels. Now I know why they made me pay in advance.

Finally, I found Massage Envy, a national chain, and all their therapists are licensed and speak great English. Why do I care if they speak English? Because I need to tell them not to work on my upper arms because they bruise, but work hard on my back, and please don't yank down my underwear and leave my butt flapping in the breeze. Furthermore, I would prefer that you not get on the table and straddle me to get at my back muscles... especially while my butt is flapping in the breeze... etc."

Also, at Massage Envy, sometimes you get someone like my new favorite person, Michelle, who has further qualifications and works in physical therapy. She, after 20 years of no answers, traced the pain in my shoulders and arms to my neck. My neck doesn't bother me, but as she worked on it, I felt "referred pain" in my arms. Ah, so the pain in my arms is starting in my neck. Getting warmer. (For all this time, I've been wanting to get to the bottom of this, to know where the pain was coming from, and to put an end to it!)

"So this is starting in the neck- why is my neck so tight?" I asked myself and the universe. for starters, I've been watching TV from a loveseat that is at a 90 degree angle from the TV. So, I watch with my neck turned. I stopped that. I didn't notice huge improvements, but there's certainly no argument to be made in favor of such a habit.

Then, one night I was watching TV and in the dialogue someone said to their coworker "Are you a clencher? I can see you're a clencher." Meaning, do you clench your jaw habitually? Why yes I do. I already know I'm a tooth grinder when I'm asleep, but I've also noticed that if I open my jaw throughout the day it makes this awful crunching sound like someone crinkling plastic bags. If I wiggle my jaw around a bit, it will loosen up and stop making that sound.

So for the last few days I've been checking my jaw every 5-10 minutes and loosening it back up until it stops "crunching." Oh yeah and I altogether gave up chewing gum, one of my long-standing vices. I had switched to a "healthier" gum that has no aspartame, but I realized the constant chomping when I have neck pain and jaw tension is... well, stupid.

Maybe it's coincidence, but I haven't needed pain meds for the last 4 nights in a row. No percocet, no advil, not even aspirin. No pain creams, no heating pad, no TENS unit, no asking my husband to rub my shoulders to get the "crunchies" (adhesions) out. Could it be my healing answer came to me in the form of a rerun episode of "Crossing Jordan?" Well, it *is* a detective show...

I hope to report back to you in a week, a month and a year to say, "oh yes, that's all behind me now. I'm clench-free and pain-free still! Can you believe I suffered for 20 years and no one ever said 'Hey! unclench your jaw!'"

Here's something that backs up my theory of where my pain really comes from:
"When teeth are held together or the jaw is held tense over a period of time such as when concentrating, the facial and neck muscles become fatigued and painful. Morning and afternoon headaches, difficulty chewing, neck pain, and sore facial muscles are the most common reported symptoms. When clenching becomes chronic such as day and night, many severe muscle related symptoms can occur that can have dramatic effects on a patient's quality of life. This leads to a painful muscle condition called myofascial pain syndrome."from http://www.tmjtreatment.com.au/common_causes.htm

If you look up myofascial pain symdrome, it sounds a lot like fibromyalgia, something I was diagnosed with at one point.

I know a number of you who read this blog also experience chronic pain. It's draining. It saps you of energy, joy and sleep. If you suspect you're a chronic clencher, the only way to know is to unclench so you know what that feels like, because clenched feels "normal" to you.try it- open your jaw wide (don't force it), like a surprised ventriloquist dummy and see if you hear any "crunching" or feel any resistance when you do it.

If something here resonated with you, maybe you are a clencher too. Are you? It's just a habit, and habits can be undone!

Well wishes and clench-free jaws-
Carla

Carla Ulbrich

The Singing Patient: Author, Humorous Songwriter and Entertainer

_____________

www.thesingingpatient.com- performance  info and dates

www.youtube.com/user/carlaulbrich - funny songs

www.linkedin.com/in/carlaulbrich

www.twitter.com/singingpatient

"I am reading Carla's book How Can You NOT Laugh at a Time Like This? and loving it. I LOVE Carla's songwriting, so I'm not surprised that her prose writing is as smart, funny, and insightful as her music." - Christine Lavin

get Carla's book! http://tinyurl.com/348hroc

Thursday, April 21, 2011

Product review and giveaway: Pain Relief Cream "Topricin"

Welcome to the first-ever product review/ giveaway on this blog!
The product we're reviewing and giving away (one gift basket only) is Topricin, a homeopathic pain relief cream.

I've been using it myself for the last few days. Conveniently (or not, depending on how you look at it), I've had significant discomfort this week after driving 800 miles in one day (by myself). So I had some legitimate pain to try out this cream on. And I gotta say, it really helped.

One the pain scale of 0-10 (zero being "no pain at all" and 10 being "i'm going to jump off a roof if this pain doesn't stop!"), I'd say for me this cream is completely effective all the way up to an 8-level pain. If something is 9 or 10, I'll try the cream first, then if it doesn't work, resort to taking advil or some other pill out of my cabinet.

Because no pharmaceutical or over-the-counter drugs are without risk (or side effects), I am always in favor of finding a more natural solution to life's little problems (and the big ones, too).

Topricin is all natural. Being homeopathic, it works with your body to heal the source of the pain, rather than only suppressing symptoms. Although it does also relieve symptoms.

The website suggests using it for some very painful conditions, including fibromyalgia, plantar fasciitis, carpal tunnel and neuropathy.

Topricin, from what I can tell, comes in 3 formulas:
1) general pain relief cream
2) "junior" pain relief (for kids)
3) foot pain relief

They are available in tubes, tubs, or "single serving" packets (great for travel/ in your purse or backpack). It's non-greasy and has no smell. I give it 2 thumbs up!

So, I have this big beautiful basket of topricin to give away!



How to enter:
  1. Mandatory:  In order to enter to win, just leave a comment on this post. Don't forget to include your email address (ex: SpiffyStuffBlog at gmail dot com --like this to avoid spamming from bots).  You can't win if I can't contact you.  ;)  This counts as one entry.
  2. Optional:  
    1. visit me on youtube (www.youtube.com ), find a song of mine that made you laugh, and come back here to tell us all about it in a comment. Again, don't forget to include your email address
    2.  Instead of limiting this contest to those who follow my blog, I'm going to make following this blog a separate entry.  Make a separate post saying that you follow this blog.  Again, don't forget to include your email address.  This counts as one entry.
    3. "Like" (hit the "like" button) Carla's music page on facbeook (http://www.facebook.com/ ) Please post your Facebook username (probably just your full name) so we can verify this entry.  Again, please include your email address.  This counts as one entry.
    4. Advertise this contest: A Tweet, a Facebook mention, a blog post about this contest on your own blog, anything like this would count as an additional, separate entry.  Be sure to post links or usernames so that your shout-out can be verified.  And finally--don't forget to include your email address.
This contest will close promptly at 10:00 p.m. EDST on Wednesday, May 18, 2011.

Shortly thereafter I will pick a winner based on their post number which will be picked by the free number generator at Random.org.  I will post the winner here for all the world to see, and notify the winner to see where/how to ship your fabulous gift basket of Topricin.  Once the winner has been confirmed, we'll send the prize your way.   

Meanwhile, you can visit the website of this giveaway's sponsor right here:
http://www.topricin.com/


Carla Ulbrich, The Singing Patient,
is the author of "How Can You *Not* Laugh at a Time Like This?"
Get Carla's Book at Amazon.com
www.thesingingpatient.com

Friday, October 22, 2010

Fibro relief

At this point, I no longer have fibromyalgia symptoms and haven't for a while.
I attribute that to... well, not any one thing because I'm usually doing more than one thing to improve my heath, and it usually takes more than one thing to do just that.
In my case, I (finally!) gave up diet soda and anything else with nutrasweet in it, and went on a gluten free diet, both about 2 years ago. Since then I also resumed acupuncture, have done chi gung, sometimes more consistently than others, and I walk 30-50 minutes a day, 6 days a week.
I haven't had symptoms in a long time, aside from unrelated tendinitis in my right shoulder. That i am dealing with via physical therapy.
However, a friend of mine just got diagnosed with fibro so I was giving her some advice and was looking for some links on the web so she could do a little reading, and I found this great site with lots of good info all in one place. So I figured hey I'll share with on my blog. Not uncommon for people with lupus to also suffer from fibro. Here ya go:
http://www.basic-keys-to-natural-health.com/all-natural-cure.html

One last note- If i want my fibro to recur, all I have to do is go jogging. Why, I don't know, but that is my experience.

Well wishes!

Sunday, December 13, 2009

pain management

For 17 years I've been battling shoulder pain. I blamed it on the lupus/ fibro, because it showed up at the same time as the illness, but it seems it might instead be connected to my guitar playing habits. Regardless of the cause, it still freaking hurts and keeps me awake most nights. Because I'm now taking low dose naltrexone, I can no longer take the very effective narcotics my doctor prescribed me.

I've also been told for years to avoid advil, of which at one point I was taking 12 pills a day- because it damages your kidneys when you take it habitually. That was upsetting to me, because Advil was so effective and non-narcotic; it didn't make me sleepy, or have any other effects that I was conscious of.

I'm getting acupuncture again, which helps some, but my habits of guitar playing and long drives (my job, in other words) kind of undo the treatments, so I'm still suffering and trying to find ways to manage the pain.

So, I was pretty glad to to hear that ibuprofen is now available as a gel. I got a voltaren Rx from my rhuematologist, but i first heard about the gel's availability from a friend who bought some on amazon.com.

I'm also a fan of icy hot, but you can't use icy hot in combination with a heating pad, which I like to use when the gel isn't enough.

I also sometimes use salonpas capsacium patches, which you can leave on for 8 hours. They can feel a bit like ripping off a bandaid when you remove them, but if you coast them with oil before removing, it helps a lot (I use olive oil even though it grosses my hubby out to be using food products on skin. Well, at least he's not kinky.).

I also have some flexor patches, which are ibuprofen patches. I didn't find them quite as helpful as the gel, which I also use on my foot (I'm not entirely cured of the Morton's neuroma, the inflamed foot thing i developed this past summer and got a couple shots for).

I also have a TENS unit, which has been really helpful at times.

And a suction cup massage device!

And relaxation CDs.

I'm trying an all-natural pain cream recommended by someone on a discussion list. She got it from iherb.com (use this discount code at iherb.com and get $5 off any order: DIT074 )

Anybody else got some good tricks you'd like to share?












Monday, June 8, 2009

stresssssssss (and lupus)

just got back from the doctor. sed rate=66, temp= 99.8. :(
my strict vegan + gluten free diet is not enough to counteract all the stress.
stress? what stress? Well, I got tons of work in March, plus I filed for bankruptcy, which really freaked me out, plus I'm writing a book, plus my mom sent me 20 boxes of moldy crap that I've left in their basement since having a stroke 7 years ago, which sent me into a fibro attack. I recovered from that only to end up with either morton's neuroma or plantar fasciitis (constant excruciating foot pain- unless i don't ever put any weight on my foot whatsoever, even to get up to go to the can). I went on "vacation"- meaning, we drove 2500 miles round trip, it rained the entire trip and i was in constant foot pain. While on "vacation" I went to a foot doc and he gave me vicodin. All it did was make me sleepy. My foot was still killing me. I finally go some acupuncture and aspirin and it's doing much better, but now I'm freaked out over the string of lupus-ish symptoms- fibro, swelling joints, foot pain, positive lupus lab results... Smells like i'm sliding back downhill towards either a hospital stay (NO!!!!) or prednisone (NO!!!!).

Sometimes I wish I were an "earthling" and I could just have a beer (not an option) or go for a jog (not an option) to blow off some steam and de-stress. Or drink a ton of coffee (not an option) and just power through the stress (not an option). The fact is, once you've got an autoimmune condition/ tendency, you have to make hard choices every day. One of my friends a while back suggested we go shopping and have dinner in the evening, and maybe earlier that day we could go do something else. I had to explain - to both her and myself- that i can only do one big thing a day. If I schedule 2, I might survive them both, but there won't be enough of me left to enjoy the second one. And it will ruin me for my one big thing the next day.

If I pace myself, and do only one big thing a day, I could very well end up doing 365 really neat things in a year. Well, maybe only 300, because sometimes my one big thing is laundry. Still, 300 neat things in a year is pretty great- barbecues with friends, going to the arcade, doinga comedy open mic. But if I don't pace myself, I can end up wasting a lot of time flat on my back in bed watching reruns, staring out the window, and popping pills to kill the pain.

The good part about knowing you have limited resources is (hopefully) you don't squander them on stupid stuff. One of my friends is raising 2 kids (he's a stay-at-home Dad and his wife has a corporate job). At night, he pursues his dream of being a songwriter. Well, being a husband and dad, he can't be gone all night every night, and he's busy all day with the kids- so he has to choose his opportunities wisely. And he tells me this helps him make better choices about the gigs he takes and how he spends his allotted "songwriter" time. It's not just those of us with serious illness having to make hard choices. And given the choice, like everyone else, if I could swap lives with my friend I would not. I've got some skills for dealing with the "devil I know" and would be overwhelmed if I had to learn an entire new set.

I can deal with this. I just need to vent sometimes.

i was able to talk my rheum out of putting me back on prednisone (for now) (I'm just not ready to lose my looks and my locks a 4th time if there's a way around it) and just get some fancy aspirin and topical anti inflammatory. but i'm going to have to start getting lots of acupuncture and learn to handle stress better or I'll be in for hospital stay/ prednisone hell #4. stress is the worst thing for autoimmunity, and stressing about autoimmunity is the strangest irony i can name at the moment...