I have a tumultuous relationship with my mind. It's a beautiful and terrible place, one I know a little better for not having had as much external stimulation in recent years. My knowledge of it has alerted me to the fact that it could do with a little cultivating.
I am prone to wandering thoughts, epic social post-mortems, shallow breathing, fear of sitting in physical discomfort, worries about how I can't keep going, and a desire to flit between distracting medias to avoid reality, which makes me less content and more terrified of existing fully in the gift of the current moment.
Several medics have encouraged me to explore the concept of mindfulness, and just after the latest encouragement, a friend alerted me to an online, free, six week course through Monash University. I have begun it, and it's bite sized and very encouraging.
You can still join now, and exercise your mind:
https://www.futurelearn.com/courses/mindfulness-wellbeing-performance
Wednesday, September 21
Thursday, September 1
going out when you're homebound
I did it
again, a house leaving excursion which didn’t go extremely well. The last
couple of months there have been very few excursions and a 100% didn’t-go-very-well
rate. But things seem almost possible in pajamas whilst lying on the couch, and
I decided to make a trip to pathology collection, lured by sleep. I’m really
quite straight forward when it comes to motivations; my mind is trained on my
next sleep, and my next eat. I knew Mum could drive me in the afternoon, but
if I went by myself in the morning then I could rest aaaall afternoon and
potentially not be some kind of aching grey puddle in the awful hour that is
waiting for Ben to get home from work. The golden rule of being Marigold’s mother:
Do not use up energy late in the day or you might run out before parent no. 2
arrives home.
If you’re
feeling dizzy while changing nappies and putting on proper clothes you shouldn’t
hop in the car. I know this. But I wanted a peaceful afternoon, so I wobbled
on. And it feels so momentous to go out when you’re not used to it, the world
feels very big and interesting after a small house.
In the car
my right eye was swelling with uncomfortable tears. I am one of those people
who gets colds in their eyes, and my eyes weep at their own sweet leisure through
the day making me appear excessively emotional. I could vividly imagine them
starting to run the second the needle went in, and assuring the nurse that I
was not crying from the sting. Smarting eye, dizzy vision, cars and trees
swooping by...regret was taking hold as I prayed through my short and dangerous
drive.
There was a
decent wait before it was my turn. Enough time to really thoroughly crumple. I
usually make it my mission to avoid hunching and crossing my legs and conducting
myself in a terribly gauche manner. But there I sat on one half of the ample
chair, arms folded in on myself, wearing a grey top, eyes smarting, slumped over.
Aware, but not correcting myself.
My mind
began to race, about how to make it home – can’t get a taxi home with a baby
car seat...this was unwise, I’m stranded...could Ben take me home in his lunch
break, but that’s not fair because he’s been off work for me all week...but
miracles happen all the time, I might be ok.
I eat a
banana, get a glass of water. Neither seems to revive me.
It’s my
turn, and the nurse and I smile at each other and acknowledge that we have met
before. Many times, if we're honest. I prefer being pricked by her to anyone
else. I remember that when I was pregnant and throwing up here there and everywhere, she stashed a few vomit bags in my tote because she knew I'd appreciate them.
The paper
work takes a long time, maybe because I’m getting genetic testing, and I try to
bolster my baby’s patience with all kinds of handbag treasures. I’d saved the
car keys till last, my piece de resistance, but they don’t seem jangly or spiky
enough for her today.
“Did you
fast for these?” She asks, forebodingly.
“No, I didn’t.
The slip said non-fasting,” I reply.
“Ah yes. It
does. I’m afraid one of the tests does need to be fasted for...”
No.
I’m so
overwhelmingly drained, I’ve given so much to get my bloods done. In another
life, I would have covered my dismay and said, oh that’s fine, never mind, I’ll
come back another day. But I’m too tired, of being sick and being impeccably
charming. I don’t hide it.
“Oh.
Really. That’s a real shame. Because I’m not very well, and it’s going to be
hard to get back here. And I also don’t know how I’ll go fasting because I need
to eat through the night to sleep. I think I’ll have to get someone to drive me
in another day.”
“Well, we
could take them anyway, when did you last eat?”
“A minute
ago. No, let’s not muddy the results.” I say
“You know what;
I live just one suburb across from you. I could drive past your house on my way
to work tomorrow morning and take them for you?”
I’m stunned
by her kindness. I know this is an out of the blue offer, not a service offered
by the practice. I know she is just being the kindest nurse in the world. I
tell her how much it means, but that I couldn’t let her do that. We agree that
we will take most of the tests today, and I’ll take the other one next week, on
Ben’s day off. She says if I fast from 2am, it should be ok.
My eyes don’t
weep during our appointment. I leave the practice. Her kindness upped my energy
in a good way, it gave me just the right amount to get myself safely, if a
little precariously home to my couch.
The gift of
health is more absent than ever, but in its absence is an ever growing pile of
radical kindnesses, spiritual epiphanies, and sweet unfoldings, which seem
acutely precious.
Tuesday, August 16
essence of sad
Have you been so sick for so many years, that you lack the will to go on?
They
say health is the most important thing, cheerfully they pronounce it,
to inspire their gratefulness,
to wash away their great unhappiness.
But you don't have health.
You don't have well.
They say friends too, they are better than career you know.
Career, it went, but friends you have.
You have friends you rarely see,
friends you hold on to, but always fob off.
You love them from your couch, but it isnt enough.
You don't cook for them, ever, and you're always writing to say
'less than an hour, but I love you ok'.
I'd love you better if I could.
My mind loves you. I swear.
They say happiness inside, that's up there too.
Peace for the ride.
And you have that one. But with essense of sad.
You want it unconditionally.
In the sore, crawling, lonely, drought.
But it morphed into sad, behind your back, so now you feel bad.
That you're sad.
Sick bad, and then guilt bad.
And lonely bad, and too-long bad,
And hermit, outcast, worthless, cold,
too-much, and can't-go-on bad.
Till the sun pops out.
It kisses you and hugs you and shouts:
It's a beautiful day to be alive.
Alive.
You have alive!
And alive is meant to be here,
and meant to be here is purpose,
and purpose is go on.
Labels:
acceptance,
chronic illness,
contentment,
depression
Thursday, August 11
hi struggler, have you tried...?
It's been over 300 days now since I
gave birth, or kind of gave permission to have my stomach cut open. I said,
"I can't read all that stuff about dying or never walking again, so I
consent but I'm not looking at what I'm consenting to," and signed a blotchy
left handed signature, a Freudian smudge, thinking to myself, I probably will
die of panic, or feel the surgery and then die, and I hate this idea and being
an adult even though I simultaneously love that my body grew a baby, and I bet
she's not even as sick as you think, I bet she's perfect, and I really hope we
both live.
And we both lived. We have lived
strugglingly and lovingly ever after.
I'm accustomed to struggles, as are
most humans. There have been a couple of uncanny similarities between chronic
illnesses and the more woeful parts of parenting, which sounds like a miserable
thing to say, but it has happily made the whole experience almost
familiar.
I went to an opshop after not sleeping
through the night for nine long months, and having chronic fatigue and another
illness, and the man at the counter said perkily, "You look well
rested!" I fumbled for a reply, but I was so absolutely unrested I could
not think of one. Awkwardly I murmmed something about resting during the day.
To which I'm sure he thought, see, these housewives just sleep all day, no
wonder they're well rested. I have a feeling he either isn't parent, had a
unicorn baby who slept in a cot and through the night before it walked {please may this happen to us, there's still time, please}, or snored through
his offspring's night time howls for comfort. Or maybe he suspected it had been
a while since I'd received a 'fresh as a daisy' type of comment, so he took it
upon himself to deliver it.
Whatever the case. Have you seen me lately?!
Probably not, because I'm too tired to leave the house. But the dark moons
under my eyes, they take pleasure in shocking me when I pass mirrors. If you
looked up my Google searches which you must never ever do because you will
think I am unfit to be an adult (I never wanted to be one anyway) you would
find ,"how to make eye shadows go away?" written all different ways
to get the best search results possible. They said: Get more sleep. I closed
the tabs. They have no idea, they have not met my child. They said: Wear make
up. That's not 'away'. That's hidden under paint, and I don't like that when I
take paint off I feel more fugly. They said: Wear cucumber circles. I don't
think we even have cucumber because I'm too sick to go to the shops and Ben
doesn't buy them because they're not carby enough for me, and I don't lounge
round in a bathrobe with slimy disks over my eyes because that's not keeping
half an eye on my charge. I didn't find one single thing that would help, not
one glimmer of hope. And then I started finding white hairs, aged twenty five
almost twenty six.
Google, Google, on my phone: how
come my hairs are already snow white?!?!
Google said, genetics. I said, sleep
deprivation too.
Anyway, I am not well rested. I used to feel unwell after
sleeping from 9.30 pm till 8.30 am only waking to coldy inform my bedmate that
he was snoring, but now I'm lucky to get till 12.30am in one stint. So, I feel
tired-dead-tired-dead, as I expected to. Tired isn't a good enough word. Wasted. Or
my favourite for this year: Haggard.
Humans have been trying to make
other people's lives better since the first suffering. I have a serious case of
it, though I'm trying to reform. It's a way of loving, it can also be a way of
irritating. Early on, just after my diagnosis, people who had never had this
illness used to say 'have you tried this expensive treatment and this almost
extinct herb and this quack of a doctor and this unlikely and exorbitant retreat
you can't afford because you're on the pension and this mental health book and
this YouTube video, because I think it will cure you?' Every second day. I
tried so many things I can't remember them; things which seemed affordable or
scientific or whatever. Mostly I only tried the advice of actual sickies,
because the other people had read something about my illness for one minute,
and myself and my friends had been reading for years.
And then came along my baby, who doesn't sleep if she isn't
touching me or Ben {slash using us as her mattress}, and 'doesn't sleep through'
which is code for 'normal non-unicorn baby'. You know when you accidentally let
slip that life is hard? Help arrives! So fast you're not even sure if you asked
for it! Usually, a vast array of suggestions you've already dismissed. There
was a flood of kindliness in the form of, "have you tried warming her bed
up, or rocking like this, patting like so, going to a sleep clinic where you
won't sleep for five nights and will consequently end up in hospital with
vertigo again, or making her cry till she gags and then gives up because she
knows you're never coming back?" And "Have you tried solids, solids,
solids?" And "Oh, she doesn't like solids? Mine does. But, I love my
food!" Ah. Well that solves the solids question. I only eat with gusto seven times a day.
All the comments were relevant to
different kinds of mini human beings, but not the kind I have. And amidst all the kindly comments came this one,
"You guys are troopers. These
sensitive koala babies are really hard work, and you're doing so good. You'll
get through one night at a time. "
No advice.
None.
Even though she was the best poised
to give it because she's mothered one just like mine. There were also people at
church who made us dinners, and said, we struggle too, we have no advice, how
can we help.
As it is with the sick ones. They don't hand out advice,
because they know that of course you've tried, and you will ask. Or that you
have no choice but to endure, and you merely need a kind word.
They're
strangely familiar, these fresh struggles. We have met before.
An issue not easily resolved. Plodding on, sometimes hopefully and peacefully, and sometimes with bitter lead in my veins. There's always the poignant symptom I am well acquainted with: the struggle to feel untainted happiness for the ones who have what I don't.
It bears the hallmarks of my longing to be well, and my friend's longing for a partner, and my other friend's longing for a child.
This year it just hit. Deja vu. It's all the same, when you simmer away the specifics.
An issue not easily resolved. Plodding on, sometimes hopefully and peacefully, and sometimes with bitter lead in my veins. There's always the poignant symptom I am well acquainted with: the struggle to feel untainted happiness for the ones who have what I don't.
It bears the hallmarks of my longing to be well, and my friend's longing for a partner, and my other friend's longing for a child.
This year it just hit. Deja vu. It's all the same, when you simmer away the specifics.
We're all
the same.
We've all just weary and in need of a kind word. A really kind word.
We've all just weary and in need of a kind word. A really kind word.
Labels:
CFS,
ME/CFS,
motherhood,
POTS
Wednesday, June 29
if you want to understand me, voila.
Many thanks to fellow CFS sufferer Jessica for making an extremely accurate infographic of my life.
Our lives.
And thanks to my fellow spoonie Lauren for sharing it with me.
Labels:
CFS,
chronic illness,
ME/CFS
unexpected
It’s a
chilly June morning. The cold lights a red swollen fire in my throat and keeps
it burning all season long. “I’ve got a virus at the moment,” my sister warns
when I ask her if she’d like to join me on a walk. “Oh no, me too,” I reply. I
mean, I have a glandular fever flare like last week and the week before,
because it’s permanently active. When I expend extra energy, resources my body
usually uses to control the virus, things become a fiery hell. A day in bed. It
sounds fairly innocuous. But then again, all things seem innocuous in small
doses, and I have a full time job now. We made a decision earlier in the year
that we would either move to a warmer climate or buy a winter-long supply of the
only thing that helps. The thing is not at all cheap, and not at all vegan, but
it helps contain the flare radically. We ship it on bulk from the US. It is
made from a calf’s thymus gland, a protein that my immune system needs more of
to fight infection.
But I
digress from the cold morning. I hustle to eat breakfast, tidy up the lounge,
have a shower, because I have to lie down at 8.30 am with the poppet. Aurelia sleeps
radically better next to a human, and we made a decision to stop the
cot fights and fails, and co sleep for now. I only resent needing to nap with
her when I compare to the women whose babies sleep alone, in cots. Comparison
is especially the thief of joy in parenting. I know some mums get ten entire
minutes to sip a hot drink all by themselves because they share it on social
media. I fantasize about cleaning the bathroom without my often groaning
spectator. On the weekend I was whittling through the flesh in my lobes, trying
to re-pierce my neglected holes because my morning slot is a mad rush to get up
and get back to bed.
Neither Aurelia
nor I believe that we need to go to sleep at 8.30 am. We lie down thinking this
is quite unnecessary, and that of course we can both stay up all day. But in a
few minutes she surrenders, and as I surrender to mothering her in this manner,
a sleepiness I could have sworn I would not feel, creeps into my eyelids. Maybe
this isn’t such an encumbrance after all. Maybe this is actually the perfect
thing.
The irony
does not escape me. I feel a lot worse on days where I busy myself in these
sleep slots. My baby, whose sensitivity and high demands require more hands on
mothering than I’d expected, her needs also force me to lie down twice a day.
An unwanted, frequently bemoaned, and yet vitally restorative practice. I do
not believe in random events, and I thank my Creator for the silver lining.
I sense
that silver linings are woven into the universe, and with time {sometimes many
years}, and a softness of heart, we glimpse them. Closer to home even than rainbows
and stars in the dark.
I grieve
winter’s effect on me, but when spring arrives and we drive through the country
and buy our first jonquils for the season, I swear I am happier than most. I
get a relief+joy cocktail appropriate to the degree I have suffered.
Having a sensitive
daughter is similar. She asks for physical contact all day and all night, and when
I recoil from the intensity, I remind myself to lean in rather than pull away
from her needs. People everywhere try to procure smiles from her, as she holds
her face with porcelain solemnity. They would like to hold her but she dissents
loudly and clams up, apart from with one person she knows well. Later in the
warmth of our lounge we are privy to the hugest smiles, most adoring eyes,
scrumptious cuddles and giggles. That leaning in to meet her needs for
security? It is rewarded with the most exclusive view of her true person. The
smile she gives me when she wakes from her nap to see me lying next to her? It’s
like the golden sun coming out, not even behind a cloud.
I’ve
written about my closeness with Ben, and the chance I’ve had to learn to sew,
the unexpected light in the pain and isolation. I love that I must always be
fit and healthy because of my diet and exercise regime. The friends I’ve made
through computer screens are intuitive, sensitive, compassionate and suffering
women who I will love for all my days. Being awake while operated on has been
my worst fear for a long time, but even that way of birthing came with a
strange glow of empowerment after surviving the ordeal. I didn’t realise till
Aurelia was born that having a tiny baby, while complicating things immensely
prenatally, also meant that she would be my tiny baby for a lot longer than
usual, and it delights me.
But there was
one sizable cloud that didn’t appear to have a silver lining. I have long
wondered what the point of my education in music and ballet was, once my body
brought it to a close. The hours and years of dedication seemed to be a snapped
branch. Did it have a place in my life beyond a wistful memory?
Only years
later do I see that without the richness the arts bring me daily, I would be
even more prone to despair. Sustaining my mind in a long illness; this is an
immense value. I don’t want to end my life so much when I have danced around
the lounge to Tchaicovsky to Aurelia’s delight, when I have listened to a
composer’s representation of all the emotions on the human spectrum and felt
understood, seen myself in the characters I read of, been transported in these
books to harder eras, and breathed in perspective. If education’s purpose is to
enable us to live a rich, abundant life, then that richness is beneficial all
the more when we move into a barren place. That richness is sustaining life. Susan
Shaeffer Macauley shared in her book this quote: “Education is a matter of the
spirit.”
I want to
get up even though I hurt, and smell the ocean again, and create a garment, and
read another poem, and hug my scrumptious baby, and eat more cake. I think that
there is an iridescent lining attached to each crushing cloud.
“There are
always flowers for those who want to see them.”
Henri Matisse
Labels:
acceptance,
arts,
contentment,
ME/CFS,
motherhood
Subscribe to:
Posts (Atom)


