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Freedom Through Fantasy

10 Things You Didn't Know About The Queens Of Fantasy Saga

July 12, 2018 Kristy Nicolle

Did you know these ten facts about The Queens Of Fantasy Saga?

INFINIFLASH FICTION

Moosings of Moo

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Feb 11, 2019

moosings of moo, Funny cat blog, funny

Moosings of Moo- A Glorious Moobilee

Feb 11, 2019

moosings of moo, Funny cat blog, funny

Evening thumb-peasant-folk, I come to you today with tales of my upcoming nine-year (toona) Moobilee.

Feb 11, 2019

moosings of moo, Funny cat blog, funny

Jan 7, 2019

Funny cat diary, funny cat blog, funny cat

Moosings of Moo- The Relapse

Jan 7, 2019

Funny cat diary, funny cat blog, funny cat

We all have weaknesses and mine, I will readily admit, is catnip. Otherwise known as Catcrack. Weed of the nipper, Kitty Ganja, the great herb of furry fucked-upedness, etc. etc. you get the idea.

Jan 7, 2019

Funny cat diary, funny cat blog, funny cat

Nov 5, 2018

moosings of moo, cattitude, Cat blog, Funny cat blog

Moosings of Moo- Rise of the Moochine

Nov 5, 2018

moosings of moo, cattitude, Cat blog, Funny cat blog

Change is on the cold north wind that has seemingly come to stay in this part of the Great British nation for which my breed is so named, and I find myself at the heart of it, as ever watchful over bae.

Nov 5, 2018

moosings of moo, cattitude, Cat blog, Funny cat blog

Moosicals Of Moo- The Songs of My People

Aug 20, 2018

moosings of moo, Funny

Moosicals Of Moo- The Songs of My People

Aug 20, 2018

moosings of moo, Funny

Cats, in case you didn’t know, are musically inclined. I am a talent beyond measure, and yet my moosical charms are lost on humans with their non-rotating ears and poor taste in dance moves.

Aug 20, 2018

moosings of moo, Funny

CHRONIC PAIN

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Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness

Confessions of a Zealous Zebra- Self Worth

Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness

I talk to a lot of chronic pain sufferers, whether that’s because I’m looking for advice, or they’re looking for advice from me. However, I always seem to end up seeing the same thing both externally and internally and it got me thinking.

Chronic pain sufferers struggle with self-worth.

Why is that?

Is it because we are worthless?

Is it because we lose our worth to these diseases?

No.

Absolutely not.

Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness

Invisible Illness, Fibromyalgia, Ehlers Danlos Syndrome, My Journey

The Invisible Man- Shining a light on the extraordinary caregivers behind the chronically ill

Invisible Illness, Fibromyalgia, Ehlers Danlos Syndrome, My Journey

“100 out of 100 relationships that involve caregiving fail.”

-Dr Phil

It’s very rare these days that I see something which makes me irritated enough to write a blog post about it. But here we are. I came across this little pearl of wisdom from Dr Phil via my friend @Queenof_thebookworms who is also a fellow chronic pain sufferer on Instagram. (Side note- she’s really cool- you should definitely go follow her if health related positivity and book love is your thing.) And I was stunned.

Invisible Illness, Fibromyalgia, Ehlers Danlos Syndrome, My Journey

Ehlers Danlos Syndrome, Invisible Illness

5 perfect dates for the partner with chronic pain.

Ehlers Danlos Syndrome, Invisible Illness

Back when I was first diagnosed, Mark made a real effort with me to keep the romance going, and came up with some simple, cheap, and cute date ideas that we could enjoy together without me having to worry about flaring up the next day.

Here are my top five.

Ehlers Danlos Syndrome, Invisible Illness

Invisible Illness, Ehlers Danlos Syndrome

5 things to remember when you can’t stop dwelling on living with no cure.

Invisible Illness, Ehlers Danlos Syndrome

I think the holidays makes people like me, people with chronic pain and invisible illness, take stock more than others, and a lot of the time I think we end up more disappointed than average Joe. It almost seems cruel that with this disease you are faced with so many unknowns and yet one unwavering certainty, that you have this thing for life and that it will limit you, that it will take things from you.

Invisible Illness, Ehlers Danlos Syndrome

Ehlers Danlos Syndrome, Invisible Illness, Fibromyalgia, My Journey

Pain and Ambition

Ehlers Danlos Syndrome, Invisible Illness, Fibromyalgia, My Journey

A lot of people ask me one question in particular when it comes to living with chronic pain.

How do you do it?

Or similarly I hear-

I don’t know how you do it.

I don’t know how you live like this.

The sad reality of the fact is, that chronic pain is my life now, and I don’t get a choice. Well, I guess I could curl up in a ball and retreat into the depths of my very comfortable bed for all time and never be seen again, but that’s not much of an existence now, is it?

Ehlers Danlos Syndrome, Invisible Illness, Fibromyalgia, My Journey

Ehlers Danlos Syndrome, Author Life, Invisible Illness, Fibromyalgia

Pain and Productivity-How I write, edit, format, and publish 400,000 words a year while battling chronic pain.

Ehlers Danlos Syndrome, Author Life, Invisible Illness, Fibromyalgia

I’m asked quite regularly how I manage to stay so productive while fighting EDS, Chronic Fatigue, Fibromyalgia, POTS, and swings in my blood sugar which affect my health, so I thought I’d give you guys an insight into how I operate. It’s taken me a good two years to perfect this routine, and more than once I’ve thought about delaying releases, so I can lie around and feel crappy in bed. Luckily for me, I haven’t so far, and I think the fact that I’m a professed workaholic without a 9-5 job really does help keep me productive.

Ehlers Danlos Syndrome, Author Life, Invisible Illness, Fibromyalgia

Ehlers Danlos Syndrome, Invisible Illness

Ehlers Danlos Syndrome- Under my Zebra-Ella

Ehlers Danlos Syndrome, Invisible Illness

Whenever people ask me about my chronic pain… I find my answers to be… how shall I put this… Lackluster. It’s a complicated thing, these diseases which have changed my life in just a few short years. Its complicated like a set of invisible dominoes you can’t see, and that most people doubt even exist. So, I am gonna try and explain this thing, this invisible thing, which most people doubt exists, in a way which is easy to understand.

Ehlers Danlos Syndrome, Invisible Illness

Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness, My Journey, Writing, Author Life

Why Freedom Through Fantasy?

Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness, My Journey, Writing, Author Life

There isn’t any question about why I became a writer. It’s that reason you never want to list as motivation, but something which often puts you on the path you least expect, and which if you’re lucky like me, turns out to be the exact place you should be.

I was desperate.

Ehlers Danlos Syndrome, Fibromyalgia, Invisible Illness, My Journey, Writing, Author Life

WRITING AND BOOKS

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Author Life, Tips and Advice, Writing

The Top 5 Self-Editing Tools For New Writers

Author Life, Tips and Advice, Writing

Now, I know what you’re thinking. Editing is what editors are for, right?

Wrong.

Any writer worth their salt must have some self-editing skills, and i’m here to show you the tools that make this process easier and more effective.

Author Life, Tips and Advice, Writing

Author Life, My Journey

Looking Forward- My 2019

Author Life, My Journey

New year, new goals, and new priorities at Kristy Nicolle Inc. This year marks a major departure from my regular author schedule and a movement into a less intense release schedule with my major focus being on marketing. I’ve spent the last 3 years building a solid backlist of books, and so this is year I’m growing my reach and getting those books into more reader’s hands than ever before. I’m super excited about 2019, so I wanted to share with you a few of the things I’m looking forward to in particular.

Author Life, My Journey

Ehlers Danlos Syndrome, Author Life, My Journey

2018- My year in Review

Ehlers Danlos Syndrome, Author Life, My Journey

It’s been one hell of a year!

My second trilogy completed, my first two signings attended, two brand new diagnoses, new medication, a visit from my best friend, who crossed the Atlantic, just so we could meet for the first time, and a personal best on all counts listed above! It’s been a busy, grueling, testing year, but according to the figures, my best one yet as an indie author.

Ehlers Danlos Syndrome, Author Life, My Journey