Five Tips for Better Mental Health with Rheumatoid Arthritis
How do you push back against the sadness,
worry, and frustration of living with RA? That’s the first prompt in the 2017
#RABlog Week and today, I’ll share what works for me.
Rheumatoid arthritis (RA) and other chronic
illnesses aren’t just physical, they affect your mental health, as well. For
instance, approximately one third of people with RA have experienced
depression, some so severe that they have thought of suicide. Having RA batters
at your body, your mind, and your soul as you fight fatigue and pain and the
stress of trying to push through it all to live as normal a life as possible. Many
of us, even if not officially diagnosed with depression, experience awareness
of what we have lost, anger, frustration, sadness, and worries about the
future.
I’ve felt all of those, in the distant and
recent past both, and likely will again. For most of my life, I was stuck in a
really difficult place where everything I did was tinged with sadness. Then that big flare
happened and after that a medication that suppressed my RA for the first
time ever.it motivated me to try a new way of approaching life with chronic
illness and disability. And it worked.
1.
Treat your condition
I really can’t emphasize this enough. Do
whatever you have to do to pursue remission
and effective pain management. Do not take no for an answer, try everything
(preferably if it’s safe and legal). It can be really difficult to muster up
the hope to try yet another thing if several haven’t worked before, but ask for
support from your doctors, your support network, and take the leap. When your
RA is suppressed, when your pain is treated, it has a profound impact on your
mood and your ability to face the world.
2.
Make friends with your body
When your body feels terrible and your life
becomes limited because of that, many of us start resenting our physical selves.
I came to hate my body so much that I disassociated from it, describing myself
as a brain in a jar — I was all personality, no physicality. Then I figured out
that becoming
friends with my body, partnering in this life with RA pain, fatigue, and
everything else that comes with it, made me feel better. Made me respects my
body more and become a whole person.
3.
Focus on what you can do
Being very aware of what you don’t have and
can’t do anymore is completely normal when you have a chronic illness. It also
puts you on the fast track to depression. Paying attention to what you can’t do
anymore and that what you no longer have because of chronic illness makes you
sad, makes you resent your body for betraying you, your self-esteem goes in the
toilet, and so on. Looking instead on what you still have and what you can still
do, even if less than B.C. (Before Chronic illness) starts you on the path to
happiness.
4. Choose
joy
The other day, someone asked me to list the
challenges in my life that were related to chronic illness. For a moment, I
couldn’t remember. For the last 12 years, I have focused not just on looking at
what I have, looking at what I can do, but actively choosing joy. It has
created a habit
of happiness that often makes it difficult to remember the things I don’t
like. This is not to say that there aren’t disappointments and sadness, just
that I turn away from it and work very hard at seeking the light. Changing my
focus and making deliberate and conscious choices towards the positive has changed
my life and made me a much happier person.
5.
Find support
None of this has come easy. It has been an
evolution that has taken years and a lot of work. As well is help. My family
and friends have circled the wagons, been there when I need to vent or worry,
as well as helped me laugh during some serious challenges. My doctors have
helped me with the medication I need to find my sense of humour when RA and
pain try to take control. And they have also helped me find counselling when
our best efforts weren’t enough. There is no shame in seeking help for your
mental health — it is an essential part of creating quality of life. If you can’t
find a counsellor (or can’t afford one), there are tools that can help you,
such as, for instance, The Arthritis Society’s online course
Arthritis and Mental Health and Well-Being.
I often say that every diagnosis of RA — as
well as any other chronic illness — should come not just with a prescription
for medication, but also with a referral to a social worker or psychologist.
Getting a diagnosis of a chronic condition is a profoundly distressing event
and changes your life. Adapting and finding your way back to living well isn’t
just about your physical health, but your emotional health, as well.
Postscript:
If you feel so inclined, a share of this post (or any other from my site) on
any channel would be much appreciated. Please be aware that for over three
months, my blog
has been designated as spam by Facebook and blocked there (without me doing
anything that’s different or inappropriate). You sharing it in a post and
indicating that it isn’t spam would be a great help in my fight to get that
block lifted.
Comments
I'll do what I can to help you out, even though I'm not on FB. (What the heck?!?)