With and Without: Rheumatoid Arthritis and Fibromyalgia Pain
Explaining the
difference between rheumatoid arthritis (RA) pain and fibromyalgia pain isn’t
easy. Articulating
what pain feels like is extremely difficult to begin with, adding an
attempt to differentiate different kinds of pain is even more of a challenge.
I have both RA and
Fibro, the latter adding on to the party in 2004. Fibro is what taught me to refer
to pain as being ‘loud.’ RA pain is deep and interior, and can leave you curled
up in a fetal position, not wanting to move ever again. Fibromyalgia pain can
be white static that makes it impossible to focus, and can feel like somebody
is blaring a fire alarm in your ear for hours.
But still, does that
tell you anything about the pain itself?
I have recently had occasion
to do some in-person research. I can tell you that both can involve throbbing,
but that’s where the similarities end.
A bit of back story
As have been evident
from my repeated whining of late, I’ve had quite a humdinger of a cold for
about a month. Because of this, I didn’t take my biologic for about the same
amount of time. And really surprisingly, I wasn’t feeling it. In the past, I
might’ve been able to skip one cycle, but then I start feeling a change.
Nothing big, but pain and that soggy feeling so unique to RA would start to encroach
around the edges.
This time, nothing. I
was fine. There was even a moment when I considered if I might have become one
of those people that we hear about in the myths who can stop their biologic and
remain fine.
Yeah, that was too
much to ask for.
RA makes a visit
I saw my doctor on a
Monday, and was still too sniffly and cough-y for either of us to be
comfortable with adding an immunosuppressant to the mix. And I was fine, so
really, there was nothing to worry about.
I should stop saying
these things out loud.
The next day something
interesting happened. After stepping away from the computer to have lunch, a
tendon in my right forearm was in a lot of pain. And not Fibro pain. This was
different. This was Serious, intense, and deep. I was a little alarmed. It felt
familiar. It felt RA-ish.
But then it went away,
so I stopped worrying.
Until that evening,
when the snow started coming in. I respond poorly to barometric changes, it
always brings pain of one kind or another, and quite substantially so.
When I went to bed, I
couldn’t sleep because of the throbbing in my feet. My toes were especially
affected, and I paid a bit of attention to them.
The pain was in the
bones, the joints, and especially the base joints in the toes on each foot, I
could feel all ten of them throbbing with the rhythm of my heart. Each throb
filled the space in the joints, pushing up against the boundaries, trying to
expand. It had that deep feeling again, echoes of sound waves at the floor of
the ocean.
RA. Without a doubt. Instant
panic.
I woke up feeling fine
the next morning, but nonetheless made an appointment to get my shot as soon as
possible. I’d call that throbbing a shot across the bow. No need to wait for
the full onslaught.
The fibro side of things
Thankfully, the shot
worked beautifully. The RA withdrew, scuttling back into its cave with a final glare
across its shoulders, and a low snarl.
And then the weather
changed, as it tends to do at this time of the year. And I found myself in a
similar situation, lying in bed in the dark, sleep held at bay by pain.
My feet were throbbing
again, especially the forefoot and the toes. I closed my eyes and paid
attention, thinking I might as well make productive use of the time and try to
compare this pain to the other.
It took a while. This
pain was hard to parse, encompassing all of the foot. I tried to listen to the
bones and the joints, but it was hard to penetrate this buzzing throb. A throb,
by the way, that didn’t have that direct line to the beat of my heart that the
RA throb does.
And then, somehow, it
came to me. The throbbing was happening in my skin and soft tissue between the
metatarsals. I could feel that v-shape of the tissue between each bone in the foot,
as well as the skin surrounding it. I could feel it because it was throbbing
and buzzing and stinging and so very present.
But I couldn’t hear
the bones. They were a negative space between and surrounded by tissue and
skin, a non-feeling, a quiet that didn’t engage with the pain.
That may not tell you
much about the pain, as such. It is more a story of its origin, and the origin's influence on the quality of the pain.
How would you describe
RA and Fibro pain?
Comments
One medication I use that greatly helps with the pain is Butrans pain patch. They come in different doses and last 7 days while providing a constant dosage of 5-25mcg/hour. They are key in controlling my pain - until I do something stupid like try to move weirdly - but allow me to keep going through the motions of daily life most of the time.
- Sarah from The House Clinics Group