Having MS is emotionally
challenging. People with MS can experience anxiety, mood swings, and
depression. In addition to symptoms being a response to adjustment to MS, some
mood symptoms could be a result of the disease process itself. Though I’m
mostly talking about the former here.
Many
people with MS go through a period of grieving after diagnosis - dealing with
the loss of certain capabilities and the uncertainty about the future. For me,
this happens over and over, with the progression of the disease. I went from a
cane to crutches to a scooter to a power wheelchair within three years of
diagnosis. I tend to be very hard on myself and hold myself to standards that
no one else ever would. I start on that downward spiral of thought, ‘What
happens if it gets worse?’
These
thoughts can trigger anxiety. Anxiety can happen in response to circumstances
in life, such as living with the uncertainty and stress of living with a
chronic disease like MS. Before I enter a new situation, I often worry
obsessively for days. Since I no longer use my legs, tricky transfers also
cause me anxiety. Anxiety presents itself in me with both physiological and
psychological symptoms. I shiver, cough and gag and am often restless. I can
also be irritable, obsessive, have racing thoughts and catastrophic thinking.
In order to manage this, I take anti-anxiety medication if I am going to be in
a new situation, and try to distract myself.
Recently, I’ve learned to
give myself a lot more breaks than I used to, and that’s done a lot to help me
adjust. I have also started Mindfulness training. If you know me, that’s a
giant step. I am pretty cynical about that sort of stuff but I have found
taking 10 minutes away from life for awhile is refreshing and if I can gain
more from it, bonus.
Remember, MS is not all in
your head. Your emotions are as valid as your physical symptoms. Include your
emotions on the list of topics to discuss with your doctor.
To learn more about
Anxiety and MS, click here.
A
good resource from the NMSS: Mood
& Cognition in MS: [What you can do]
Rachel, thanks for sharing your thoughts and perspective. There is no way I can possibly understand the difficulties of having to live with MS. Your perspective on life's challenges and willingness to open your self up to new experiences are amazing. I think of you often.
ReplyDeleteSara Knoeck
Thank you Sara.
DeleteDo you use guided meditations? I've been using Headspace. Jury is still out.
ReplyDeleteI downloaded the Headspace app and have been doing their 10-minute free meditations. I like them. Enough to pay for them? We'll see.
Delete