How does the old saying adage go? What a difference a year makes. And, my recent experiences can only substantiate this.
Regular readers of the blog will remember that last year, I experienced my very first cruise and that unfortunately, it did not go as well as my parents and I had hoped.
The symptoms associated with this neurological condition were consistently present and remarkably severe that it affected my enjoyment of the holiday and also left me unable to disembark the ship and see the beautiful places that I was so looking forward to visiting.
Fast forward a year (okay more like a year and a half), and I am back from yet another cruise! Why go on a cruise when the first one did not go well, I hear you ask.
Well, the large part of the reason why I decided to go another cruise, is that I refuse to let the neurological condition that I live with have any more control over my life than it already has. I came across, a perfect quote that sums this up brilliantly; this quote says “Life begins at the end of your comfort zone.”
And it is true, if we only stayed within the confines of our comfort zones then we would never know what we can be capable of, or what we can achieve when given a chance.
[Tweet “If we only stayed inside our comfort zone we would never learn what we are capable of.”]
The symptoms that are as a result of the brain stem lesion already makes life difficult, for example, visiting certain types of places such as those with high ceilings and fluorescent lighting are very challenging for me as they increase the severity of symptoms such as dizziness and vertigo.
As a result, I do not wish for my condition to stop me from doing anything else that I want to do, including taking trips abroad.
Flying and therefore requiring to spend hours waiting in an airport would not be compatible with my symptoms so consequently, a cruise offers an alternative for me to be still able to travel. Furthermore, the rational side of me also realised that although I found the first cruise particularly difficult, it does not necessarily mean that I would have the same experience on future cruises.
Back last year, just a few months after arriving back from the Mediterranean, my parents and I booked a second cruise with Royal Caribbean on their brand new ship Anthem of the Seas travelling this time around the Canary Islands (as well as stops in Spain and Portugal). And I am so glad that I did!
This cruise went much better than the last one and even managed to get off the ship twice, leading to spending a few hours perusing the streets of Tenerife and Madeira.
The process of disembarking the ship and then having to find our way to wherever we wanted to visit was not easy especially giving the severity of the symptoms, but I still managed to push through and achieve something I did not think I could do. To some, getting off at only two stops may not seem like much, but fellow spoonies would appreciate the enormity of this feat, especially when battling constant and unrelenting symptoms.
Anthem of the Seas is a fantastic and beautiful ship, and Royal Caribbean has seriously gone hi-tech. Before embarking on the cruise, we bought an internet package, and was impressed with the speed of the bandwidth, enabling me to stream movies and television programmes on my iPad occupying my time when fatigue set in (which was a lot!.
The WOW factor did not stop there, however; all over the ship, there was amazing artwork to marvel at, often feeling like Alice landing in Wonderland. What I love about Royal Caribbean, is the thought that has gone into the design of their ships; all public areas are fully accessible and have automatic doors making it easy for those in wheelchairs to be able to navigate their way around the boat unaided.
The food was also stunning and particularly loved having a wide variety of choice of where to have dinner. We sampled the delights of the majority of the complimentary restaurants onboard but spent most nights dining in the American Icon Grill. One night, however, we chose to pay extra and ate at Jamie’s Italian where the food was delicious and the staff attentive and friendly.
The highlight of the cruise for me, being a fan of Queen was seeing We Will Rock You, which was incredible and rivaled any West End show. My Mum and I also paid extra to use the facilities in the spa, which included an aromatherapy steam room and sauna, as well as the use of hotbeds which not only did I find incredibly relaxing but also really helped ease the often excruciating pain in my legs.
Strange though isn’t it? Last year, I was unable to get off the ship and generally found the whole cruise experience extremely difficult.
A year on, however, and despite my symptoms not improving in that time I found this holiday much more comfortable, even managing to push the boundaries of my comfort zone.
Why is this? Perhaps the reason is that during the past since the first cruise I have managed to push myself further, expanding the perimeter of the small world that my neurological condition has forced me inside. Examples include conquering going to the cinema, a pastime that I used to love but is now extremely difficult for me as a result of my severe and unrelenting symptoms and as a result started to avoid. By pushing myself to go to places and placing myself into situations that increase the severity of my symptoms, and achieving staying in them, reinforces the belief that I am stronger than my condition and can get through stressful situations.
[Tweet “By going beyond our comfort zones shows us that we are stronger than our illness has us believe.”]
Or perhaps I have reached a new, deeper stage of acceptance.
Accepted the reality of the diagnosis of a long-term neurological condition – that is not to say that I have given up and surrendered to the disorder but rather let myself go of the suffering that came from continuously fighting against the symptoms and the hold that they had over my life. I have accepted that I will always have difficulty with certain situations and the majority of things will not be easy for me, but what I can control is my reaction to them, and by doing so I can learn to be in control of my symptoms instead of them controlling me.
[Tweet “Acceptance has helped me learn to be in control of my symptoms instead of them controlling me.”]
In the end, I had to accept the reality of the symptoms; accept the long-term presence of them in my life. And by doing so, I no longer fought the presence of the symptoms but acknowledged their present existence at that moment. I have freed myself from the prison of fighting against the symptoms, and avoiding certain places and situations has placed me in.
By accepting the reality of life with a long-term condition surprisingly made it easier to cope with the symptoms and all of the ups and downs as a result of living with a chronic illness. I was able to find little coping strategies that helped minimise the effect of the symptoms and help me stay in control of the symptoms rather than the symptoms controlling my life.
Of course, there are days when it feels that the symptoms still have control over my life but by accepting the reality of life with chronic illness, getting through the bad days is easier than before.
Above all, going on holiday on the cruise of a lifetime has made me realise that being diagnosed with a chronic illness, or disability does not spell the end of our lives or even our dreams.
Yes, perhaps the route to which we can reach our goals and dreams may have to change, but we can still reach that final destination. Chronic illness should not mean the end our dreams; we can still follow them if we took a leap of faith.
[Tweet “We can still achieve our dreams and ambitions if only we took a leap of faith.”]
It is this realisation that I came to while on holiday – if I took the easy option and decided not to go on the cruise then I would never realise the strength and control that I can have over FND and its symptoms. And if it weren’t for that, then I would never have the opportunity to visit a country that I have wanted to for so long – Norway!
Yes, we have booked yet another cruise for next year to the beautiful and amazing country that is Norway. And this trip I can look forward to with excitement and positivity instead of anxiety and trepidation.
So all of you reading this – don’t give up on your dreams, believe me, you can still achieve them despite the challenges in your way.
Comments
RhiannLouise, I am so glad that you went on the cruise and was able to push your comfort zone and enjoy the trip. I am also glad you were able to find acceptance of your chronic illness!
I know that accepting the symptoms you have and finding ways to deal with them so you can travel is wonderful. I too have a chronic illness, ok several, but they include similar symptoms to what you described and non-stop chronic pain in my whole body and internally. I have not found the kind of acceptance that you talk about, but I work on it each day and try to just accept what my body and illnesses will allow me to do each day. Some days I still stink at it and have a mental pity party for myself, but I’m doing better than I used to in general in the acceptance catagory.
I wish I could travel like you have found you can, I have always wanted to see the world and currently am not able to deal with traveling inside the USA from Tx to some of the northern states by car or plane. I love the pictures you took and it gives a nice glimpse of the places you visited and the cruise ship, which has beautiful architecture and the neat robotic bar (or that is what it looked like to me.)
I look forward to reading more of your older posts and your new ones as they come. I’m so glad that I have met you here.
-Andrea
Hello Andrea
Thank you so much for taking the time to reply to my post (and of course for reading it in the first place!). And thank you for your such kind words. It was a very difficult trip, and much more nerve-wracking considering my first cruise didn’t go well, but in the end am so glad that I went, and although I found it difficult and tiresome it allowed me the opportunity to realise that although it may not always seem like it I am able to push myself and go beyond my comfort zone. For someone battling chronic pain, dizziness, and all the other symptoms that come with living with a neurological condition, I wanted to write the post and share my experiences of the cruise to show people that travel is still possible – it may take some extra thought and planning but still nothing should be out of our reach because of chronic illness.
I hope you are soon able to find some semblance of acceptance. You will find it when you are ready. And the thing about acceptance is, sometimes you have it and at other times you lose it again! As my mobility and legs have been worse lately than they have for a while, and the acceptance that I had found has wade somewhat.
I too am glad to have found you and your blog and look forward to reading more and getting to know you more too. And I look forward to reading more of your thoughtful responses to my posts.
Rhiann xx
“don’t give up on your dreams, believe me you can still achieve them despite the challenges in your way”
Beautifully said 😉
Lovely! Acceptance is a much better way of spending your time than fighting. Nice to see you are not letting it hold you back.
I’m so glad your second cruise went better. I travel a lot, both for work and for fun. It can be hard but nothing fun ever happens in my comfort zone!
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