Dementia Mummy is a Dementia Campaigners and
regularly writes about elder care, dementia care and MCI. However, it is important sometimes to
understand the person behind the blog.
Dementia Mummy was diagnosed Mild Cognitive
Impairment a form of mild dementia seventeen years ago, in her early 20s.
Since being diagnosed Dementia Mummy has campaigned
to raise awareness around MCI and Dementia and hopefully blow away some of the
stigmas others have whilst hopefully inspiring those who have been similarly
diagnosed. Showing them that they can
continue to live life to the full even with the condition.
Through this interview we discussed the perceptions
of Mild Cognitive Impairment and dementia, the challenges faced for Dementia
Mummies family and the strength that together Mummy and the Hubster have
working together as a team as opposed to carer and patient.
How did you discover that Mummy had MCI?
Hubster: I met Mummy online (Match.com) and we’s
been talking for about 3 months before we officially met. When we’d only been on about 4 dates back in
2008 Mummy sent me an email and told me.
I was really relieved as sometimes mummy would come across as scatty and
forgetful and her family would make jokes – it was like a joke I wasn’t in on,
this made me feel like maybe mummy wasn’t that interested. Once I knew what is was I jumped in the car
and drove to see her, to tell her I was already falling in love with her and
give her a hug.
Mummy: it was the first I love you in our
relationship… My temperament would change rapidly, and I struggled to remember
what had happen just a few days before.
I first started getting ill in 1998, Chronically tired, couldn’t
remember simple instructions or parts of my own life. My family would tell people I was PTI
(Part-Time Intelligent). The doctors
believe the cause was a head injury trauma I suffered when I was 18 but it took
a few more years for the diagnosis to be confirmed.
Did you consider the possibility of MCI?
Mummy: No, I’d never heard of MCI, I thought
it was PMS or stress from work. One Dr
said he thought it might be Chronic Fatigue Syndrome.
What were your feeling and thoughts after diagnosis was confirmed?
Mummy: I actually went back to work and didn’t
tell anyone for about 3 months I kept it a secret, I was so ashamed to be “old”
at 21. At the same time, I felt slightly relieved that I had a reason for my
behaviour. I think like dementia people
are scared of it and no one really wants to know “How you are!!!” Back in the 1990’s the internet wasn’t as
widely used as it is now so I spent a lot of time researching at the local
library using real books.
I found the more I knew and understood the more I thought I
wasn’t going to let this illness destroy me.
I still wanted to get married one day and settle with my own family, so
I had to keep going. Once I “accepted”
my condition I was able to tell my family and close friends. I was able to explain it to them and this
reduced my own anxieties and stress.
Now with the help of my family (and the love of my
children) I concentrate on what I can do, not what I can’t.
Hubster: When I found out, which was much later,
I wasn’t sure how to tell my friends and family. I asked Dementia Mummy how I should approach
it, she told me to just wait till they noticed she was scatty which she hoped
they wouldn’t till after we were married… it was that day that I knew I was
going to marry this amazing brave woman stood in front of me with her
un-brushed hair and odd shoes on.
Mummy: you proposed after that to.
Hubster: well I know how to take a hint and that
was a big one [laughs]
What adjustments have you made to live with MCI so positively?
Mummy: I have bad days, where I really
struggle to remember words to form sentences and days where just getting out of
bed is a major memory fight. I get
frustrated with myself and become angry – I have to say I’m not angry at you it’s
me I’m annoyed at.
Hubster: I’m always in trouble it’s just the
depth that varies.
Mummy: true but on these occasions, I do tell
you it’s not you.
Hubster: we try to make these instances as few
and far between as possible. I think
Dementia Mummy did the right thing by gathering as much information as possible
when she was diagnosed. I’ve been
luckier as I’ve had access to the internet which has connected me to more
people who can share stories and understand.
Mummy: it’s learning how to live with the condition,
so it doesn’t affect your life overly.
It is possible to become socially isolated through your own
actions. And it is much easier to stay
in than go out and have to deal with obstacles, like
not being able to see or hear properly, not being able to judge things
accurately or getting lost.
Hubster: it is
hard, because like in most couples one of us has to go out and work as we still
have bills and a mortgage that need paying.
Dementia Mummy stays home and raises our children (Blogger Babies) and
she uses her blog to campaign awareness.
Mummy: still
need to make money somehow though. I feel like I’m a spare part and not
contributing to the finances makes it worse.
How are you involved in raising awareness – why is it important?
Mummy: during my quiet years (before husband
and children) I would get quite depressed, so I tried to find groups and people
in the same boat just, so I could talk to someone about how I was feeling. Back in the early 2000’s there wasn’t the
wide range of dementia café’s and groups as there is now but there still isn’t
the support for MCI patients.
Dementia friends information has helped, they weren’t
running when I was first diagnosed but over the last few years they’ve been
making waves in the dementia and Alzheimer’s world.
I started to write a blog but kept forgetting to update it,
so I scrapped it in 2009. Then in 2015 I
became involved with a charity The Edith Ellen Foundation
and they wanted me to manage their social media and raise awareness across the
social media platforms of Instagram, Facebook, Twitter
and YouTube
– I then offered to restart my blog under their banner which they agreed to its
called The
Mummy Dementia and I’m quite proud of it.
In 2016, I became a Purple Angel - Norman McNamara from the
UK was diagnosed with dementia at only 50 years of age. Whilst out shopping one
day he was rudely spoken to by a shopkeeper and decided to change the way
people see dementia and treat others. So, globally we raise awareness about
dementia, MCI, Alzheimer’s and about being caring and compassionate.
I’ve not really had the opportunity to speak publicly but
hopefully one day I’ll been seen as an influencer and be recognised as having
something positive to say.
Together, Hubster and I try to get involved in as many
events within the UK, to inspire others and tell them that look there is life
after diagnosis.
Hubster: Dementia Mummy has a saying “To live is
the rarest thing in the world, most people simply exist”, I got that, right
didn’t I?
Mummy: close enough Oscar Wilde said it i just like it, it's true. It’s just so important that you try to keep
some normality about your life, you can do somethings even if it isn’t all the
things you could do before – concentrate on the things you can do and don’t set
yourself up to fail.
If you’re caring for someone with dementia or MCI, try not
to disable them, you don’t need to do absolutely everything for them – you’ll
still need to be close by to help when needed.
How important is it to talk about Dementia?
Mummy: It is so important to talk about
dementia and MCI – so many people think that once your diagnosed you suddenly
become stupid and they talk very slowly at you or around you.
I’m cognitively challenged, I can remember pretty much
everything from my childhood and teenage years – I have black holes but most of
it’s there. It’s as though I can’t
remember yesterday today but ask me again in a year and I’ll know what
happened.
Don’t
just look at a person as having dementia: they might have been a Doctor, a
teacher, a researcher, writer, a driver…and those skills they’ve had throughout
their life are slow to be removed. But
suddenly they’ve become an expert by experience in their own dementia, and that
can add value. We can contribute so much,
instead of people doing for us they should do things with us.
It’s so
important to talk about it because other people are so afraid to ask and if you
start the conversation it lets them know its ok to ask questions.
By not
talking about it you’re not enabling that pay it forward to happen and people
aren’t going to become aware – MCI, dementia, Alzheimer’s shouldn’t be hidden
away it’s nothing to be ashamed of.
Hubster: yes,
what she said. Stop enabling the stigma
raise awareness, ask those questions and get the conversation started.
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