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Welcome to the Health Activist Writer’s Month Challenge brought together by WEGO Health – a social network for all health activists.  Again, I am participating in the annual Writer’s Month Challenge in which I will be writing about my health activism and health condition based upon given prompts.

Wednesday 29th April: Product Review

What’s your favourite health-related product?  Share it with your community and tell them why you love it so much and how it has helped you on your patient journey.

The pain that I experience in legs as a result of the spastic paraparesis (stiffness and weakness in the muscles of the legs) is severe and unrelenting.  The medication, pregabalin that I take to control these symptoms, however only seem to dull the pain somewhat and as a result, I still live with these debilitating symptoms every day.

Last year, whilst on the cruise, the intensity of the pain had increased prior to leaving for the holiday.  I was prescribed co-codamol on top of the existing medication, but it only helped somewhat and found that it helped more with insomnia that I was experiencing as a result of the pain.  My Mum decided to book a spa treatment for her and myself; a luxurious 60-minute full-body massage.

Research has shown that massage is effective in helping to relieve and reduce pain.  Studies suggest that there are several ways that it does just that.  For instance, massage is thought to increase blood flow to sore, stiff joints and muscles, which are warmed by the extra circulation.  Furthermore, massage also triggers the brain to release natural painkillers as well as helping to speed the flow of oxytocin.  Oxytocin is a hormone that relaxes muscles as well as promoting feelings of calm and contentment.

It was pure bliss! After the massage had ended, I felt incredibly relaxed and found it also lessened the pain also! Bonus! The combination of the massage itself, and the oils used, which is said to ease the pain (the masseur asked of any medical issues prior to starting the massage to tailor it to my needs) really helped to ease the severe discomfort in my legs.  We were also if we would like to purchase the oils that were used during our massage, Mum purchased,  to use them at home to massage my legs when the pain was at its worst.

Massages, as I am sure you are well aware of, are incredibly expensive and as I am unable to work because of my condition, it is therefore not an alternative therapy that I can afford.  Obviously, we still had the massage oils to use, but as Mum has never been trained as a masseur, the effects were not the same!  After doing some research and after talking to people also experiencing chronic pain, I thought about buying an electric body massager to see if it would work in helping to ease some of the pain.

It would also allow me to massage my legs by myself without relying on another person, especially as I am often on my own in the house.  Being able to do it myself would allow me to be able to massage my legs when I really am in the need of one.

After a lot of online research, I purchased the Homedics Perfect Reach Massager.
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It’s great as its light-weight which allows you to be able to hard to reach areas, and as someone who struggles to hold heavy items, it’s light enough for me to be able to massage all areas of my legs.  The massager also has two different speed settings; which allows you to either choose a low setting for a relaxing massage or the high for a more invigorating massage.  I have found that on days where the pain is not quite as intense, the low setting is appropriate speed to relax the muscles in my legs; whereas the more invigorating setting really helps knead the muscles, allowing them to relax and to alleviate some of the pain.

The device also has 3 custom attachments, which includes an attachment which has a wide area for comforting larger muscles (very useful for the legs, I have found), a roller for kneading massage and a spot for targeted relief.

Using it has helped alleviate some of the pain that I experience, obviously, it isn’t a magic wand and therefore it still a symptom that I live with constantly, but is a tool that I find helps when the pain is at its worse.

And I have found that its positive effects do not just include pain management, but I have found that after having a massage I am more relaxed and less affected by stress.

I personally love the product and has a place in my comfort box as just one tool in my battle against chronic pain.

And it allows me to be able to have a regular massage without the hefty price tag!

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Welcome to the Health Activist Writer’s Month Challenge brought together by WEGO Health – a social network for all health activists.  Again, I am participating in the annual Writer’s Month Challenge in which I will be writing about my health activism and health condition based upon given prompts.

Tuesday 28th April: H.E.A.L.T.H 

Use ‘health’ as an acronym and come up with words that represent your Health Activist journey.

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H is for HOPE
As I have written in earlier posts, hope is a vital ingredient for life with a chronic illness.  Hope acts as a survival mechanism for when we are at our lowest ebb.  It is what motivates us to overcome the obstacles blocking our path, to push forward and carry on living.  Hope is the line between creating and maintaining a happy and meaningful life despite chronic illness or being consumed by the negativity that illness can create.  Hope allows us to have something look forward to when it seems our future looks bleak.
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E is for EDUCATING
The aspect I love is the reciprocal nature of being a ‘health activist’.  As much as my blog and my writing, as well as my presence on social media, helps to educate and inform others of neurological conditions such as the brain stem lesion I live with or the impact of chronic illness in general, I also enjoy learning of other chronic conditions and the impact that these create in the lives of the individuals living with them.  I have learned so much about other chronic illnesses from reading various blogs that I love reading and by getting to know others on social media; in fact, I have even been known to diagnose patients on certain medical dramas from what I have learned from other bloggers and health activists!
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A is for AWARENESS
An important part of living with a long-term health condition is self-management.  Therefore, to be able to implement a self-management programme it is important to be aware of every aspect of your particular chronic condition.  We need to be aware of potential triggers that can induce symptoms, so we can stay away from them as much as possible and not exacerbate the condition.  It is important to also be aware of anything that eases symptoms for when they do occur.  It is about making positive conscious decisions to help ease symptoms as much as possible and to improve quality of life.
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L is for LISTENING
It is so important to listen to our bodies.  Your body knows what it is capable of, and so we need to listen to them, especially if your condition is one which tends to fluctuate.  In order to be as well as possible, we need to be aware of any changes in symptoms and act accordingly.  An example, and one which I have done a lot lately, after listening more to my body, is taking a rest when needed.
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T is for TWITTER
I have come to absolutely love Twitter and use it a lot to communicate and connect with other health advocates, bloggers, and spoonies in general.  As well as using it as a tool to promote my blog and the writing I do as a result, but I have also built a lovely support network with others who or have had experiences with chronic illness.  It is a great tool to use as a way of sustaining a role in health activism, by tweeting information, links and sharing other blogs regarding the condition being represented.
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H is for Hobbies
Living with a chronic illness, it seems can often take over our entire lives.  It really does, everyday symptoms dictate to us how our day is going, what we can and cannot do, and so on. It can make us feel that sometimes we have no control over our own lives.  It is important therefore to have a life outside of illness.   One way to do that is to find hobbies and interests away from illness.   It is great to have hobbies as a way of distracting oneself from debilitating symptoms and helps alleviate the effect of them on our lives.

Don’t let what you can can’t do interfere with doing what you can do!

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Welcome to the Health Activist Writer’s Month Challenge brought together by WEGO Health – a social network for all health activists.  Again, I am participating in the annual Writer’s Month Challenge in which I will be writing about my health activism and health condition based on given prompts.

Monday 27th April: Bye, bye, bye… 

Living with an illness, you are more likely to face people who don’t understand your daily struggles.  Sometimes, those people can be inconsiderate and hurtful.  Have you ever wanted to tell them how you really feel, but didn’t feel like you were able to?  Now is your chance! Write an open letter to the people who have hurt you.  What would you say to them?  What lessons would you like them to learn?

This is a tough post for me to write.  There have been plenty in my life over the years who have failed to understand the daily struggles of living with constant dizziness.  And as a result of failing to understand my struggles, and the neurological condition that I live with, many friends have failed to stick around in my life, and have lost many friends it seems as a result of chronic illness.  It seems that you really do find out who your true friends are when you are in need of friends the most.

Many people have hurt me and dented my self-confidence.  The hurt that I have felt as a result of hurtful words or abandonment, has made it difficult for me to be able to trust people.  I am now protective of my heart, who I let in my life and who to trust.

And all because of inconsiderate, intolerant and unsympathetic people. Writing can be a cathatric experience...
To those who have hurt me, teased me and abandoned me,

Words cannot describe how much you have hurt me.  

Words cannot express how low your cruel words and actions have made me feel.  

Do you have any idea that your words and actions can have such a lasting impact on a person?  

Do you even care? 

What if it happened to your son or daughter?  What would you think, or say to those who have hurt your children?  

Would you look back on the way you have treated me and feel remorse and shame?  Or have you forgotten about your hurtful and cruel behaviour?  

I often wonder if you have, as I wish I could. 

All of the name-calling, abandonment, and ostracisation have had a lasting impact on my life, and my self-esteem.  

The names that you used to call me, still stays with me, ‘freak’ is one such example.  

We were only kids back then, and suppose because of this I am able to forgive you.  Back then, nobody, not even myself, my parents or the doctors knew what was wrong with me. I was just experiencing vague symptoms; symptoms that made me different from everybody else.  Symptoms that made it easy to be picked on.  If we were all aware of the neurological condition that made me so different from you and everyone else, would it have made a difference?  Would have you shown me compassion and tolerance instead of the cruelty and intolerance? 

Dealing with the name-calling and bullying was bad enough, but what hurt even more than that was being ostracised and left out.  To have friends turn on me and abandoning me.  I wonder what is wrong with me for people to walk out of my life; for people to walk away and never contact again.  Like I never even existed.  Am I really such a horrible person to be with for you never to speak to me again?  Does it have to do with me as a person?  Or is it because you cannot handle my neurological condition? 

I know that I am unlike most of your other friends.  I know my condition prevents me from being able to go out at night clubbing or go on spontaneous trips.  I have difficulties in places such as the cinema, or shopping malls which makes outings very difficult for me.  But is that really a reason to end a friendship?  To just walk away and never talk to me again?  I like to think I am a good friend; with those dear friends, I have made online I try and be the best friend that I can be and be there for them when they need me.  Giving how many friends that have just up and left in my life, I have doubts.   At this moment I am writing this whilst watching One Tree Hill, and watching the strong and lasting friendships develop onscreen makes me jealous of these.  What is so wrong with me, that I have never had friendships like those?  What is wrong with me that no-one has wanted to be my friend for very long? 

Although these experiences have had a lasting impact upon my life and can be attributed to my lack of confidence and self-esteem, I do not want to hold on to bitterness or hatred towards the people, like you that made me feel so worthless.  I forgive you.  Yes, I have decided to forgive you because I want to be the bigger person.   I hope that since we last met, you have learned compassion and tolerance towards those people who are different to you such as those living with chronic illness and disabilities.  

I hope that when you have children you teach them to be kind, compassionate and thoughtful towards those who are different.  

Teach them to stand up for those who cannot stand up for themselves. 

From 

Rhiann

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Welcome to the Health Activist Writer’s Month Challenge brought together by WEGO Health – a social network for all health activists.  Again, I am participating in the annual Writer’s Month Challenge in which I will be writing about my health activism and health condition based on given prompts.

Sunday 26th April: Make it a great day!

Life is full of ups and downs.  Sometimes, the type of day we have is out of our control, but other times, we can influence how our day is going.  Come up with 5 tips for changing your frame of mind when you’re having a bad day!

There is saying that says ‘Life is like a rollercoaster.’  And this saying, perfectly sums up what it is to live with a chronic illness.

Every day there are many ups and downs as a result of our chronic illnesses.

There are plenty of ‘up’ moments, little moments that make the day worthwhile and gives us a reason to smile.

However, inevitably there are just as many ‘down’ moments, usually as a result of the onset of symptoms, and other effects that are a result of living with a chronic illness.

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It is true that we as individuals have control over how we are feeling and therefore influence how our day is going.  However, as those of living with a chronic illness will relate, often our symptoms and our long-term health condition very often dictate the type of day we are going to have.

Take yesterday, for instance, as my Mum has the week off from work, we were planning a trip to a local out-of-town shopping centre, which I was really looking forward to, especially as trips out, particularly those with Mum and Dad are rare.

However, on the morning of the planned trip, I awoke feeling exceptionally weak.  During the night, I experienced excruciating pain in my legs, and in the morning, I found that they were weak and barely strong enough to hold me up, never mind being strong enough to allow me to walk around shops for most of the morning.

Furthermore, the constant dizziness that I experience as a result of the brain stem lesion was exceptionally intense.

As a result, therefore, I felt that I was too unwell to go on the planned trip, and instead spent most of the day lying on the sofa beneath my comforting duvet whilst my parents went shopping.  It was disappointing and frustrating not being able to do something that I was so looking forward to, and just one example of not being in control of how our day is going.

So, on these bad days, and the days in which we have no control over our day as a result of illness, how can we help change our frame of mind to make a bad day seem less so?  Here are 5 tips that can help change our day:

  • Practice gratitude: In my experience, using a gratitude journal and practicing gratitude can greatly help change our mindset.  In these gratitude journals, it is useful to write at least 3 good things that happened to you during the day no matter how small or insignificant they may seem.  In my experience, in my doing so it helps to change your negative mindset into a positive one, and furthermore, it also helps to make you appreciate the little gifts that each day delivers.

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    Rewarding yourself: After a long day battling with symptoms such as pain, nausea, dizziness is a feat in itself! By planning to reward yourself, for getting through a difficult and stressful day, or for finishing a task despite dealing with debilitating symptoms it can help to give yourself something else to think about besides the symptoms currently being experienced.  Rewarding ourselves gives us something to look forward to despite the stresses of living with chronic illness. The reward does not need to be big or expensive; sometimes it’s finding pleasures in the little things in life.  My favourite reward?  A delicious bar of chocolate to savour at the end of the night!

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  • Listen to a favourite song and sing along!: Research has shown that listening to music that you like can actually alter your mood and alleviate feelings of depression.  Therefore, make your own ‘Feel Better’ playlist in your Mp3 player that includes songs that work for you and which lifts your mood.  Choose positive and uplifting songs that you can sing along to, such as the brilliant ‘Happy’ by Pharrell Williams.  It could really help change the outlook for the day!

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  • Honour yourself and your body: On these days, where we feel that we have no control, is the most important time to practice some self-care.  It is important to practice these rituals when we need it the most.  Nurture yourself by taking a warm bath, schedule a massage, cozy up with a book, or relax with a cup of tea and enjoy some quiet time.

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  • Smile!: Research has shown that in fact smiling really can turn a frown upside down.  When things seem bad smiling can actually make us feel more positive and happier about the situation, so let’s all try smiling!  And surround yourself with positive people and positive things – the positivity board that I have set up in my bedroom really does help when I am experiencing bad flares as a result of my condition.  It is a reminder that the negative situation is not permanent, it’s only temporary and as everything that is brief, it will soon pass.

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Welcome to the Health Activist Writer’s Month Challenge brought together by WEGO Health – a social network for all health activists.  Again, I am participating in the annual Writer’s Month Challenge in which I will be writing about my health activism and health condition based on given prompts.

Saturday 25th April: Word Cloud 

Use Wordle to make a cloud full of words that come to mind when you think of your blog, health condition, interests or community.  Pro Tip: Use a thesaurus to make the branches of your ‘tree’ extend further.

Well, again this has been a post that I have completed before.

In previous years, I have used the opportunity to share all the words that I associate with myself and the neurological condition that I live with.

This year, therefore, I have decided to share the positive words that I personally associate with the spoonie community.

A community that I have personally been involved with for the past three or four years.

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