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Meet Aoife

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Wednesday December 18 2013 11:00 AM

'In Aoife's introductory blog for MS Ireland, she shares her MS story and how her life has changed in little ways'

My diagnosis came when I was in my final year of college. I was under an enormous amount of pressure as anyone in their final year would be. My symptoms were refined to sensory issues. I had been experiencing numbness in my fingers and toes, as well as my face over a few months. My symptoms could be traced back for years, but in relation to the diagnosis I will keep it short. I had been to my GP on numerous occasions regarding issues which I now know were MS related over the space of five months. Nothing showed up and the symptoms could easily have been stress related or nerve damage. I knew something wasn't right, but I couldn't quite figure it out. I had googled my symptoms and knew MS was a possibility, but it seemed to be diagnosed in people older than me, I now know this is not the case!  

The occurrence which lead to my diagnosis was a case of optic neuritis in my right eye. I experienced 98% vision loss. I was studying art in college, so the thought of losing my sight was devastating to me. Having googled my symptoms I knew at this point that the most likely cause of them was multiple sclerosis.

From that point I was hospitalized and my suspicions were confirmed. I wasn't upset as such. I was relieved to have identified the issue, I knew that from this point there was something I could do. Before the diagnosis I had felt extremely helpless.  

From then on life has changed in little ways. As a mother life is hectic, I need to make more of an effort to get the rest I need. At times my high heels are shoved under the bed and replaced by converse, but as my six year old tells me; 'Some people wear glasses, and some people's electricity doesn't work.'. He has it in a nut shell, he wears glasses and that is something he has to live with each day, while I have to deal with disruption to my electrical conductivity.  

We all have our issues, our labels, our baggage, but adaptation and resilience make it easier to carry on carrying on. 

Go raibh maith agat.

Author: Aoife Kirwan

Tags: aoifekirwan, artist, ms, symptoms, ms&me, blog, opticneuritis, vision

Comments

Declan

Wednesday December 18 2013 12:40

Hi Aoife, I like the glasses and electricity analogy. I was not happy to be told that I had MS all those years ago but it did make a difference to have a label on what was affecting me. If you don't know what is hurting you it is very difficult to take corrective measures.

Sarah

Wednesday December 18 2013 12:59

I also shove my high heels under the bed and put on my comfy shoes!

Thanks for sharing:) Sarah

Rory

Wednesday December 18 2013 14:27

Aoife, what a wonderful analogy to use to explain MS to a young child. I must bear that one in mind. Loved reading about your pragmatic approach to your MS diagnosis also. Well done, and wishing you a very happy and healthy Christmas and New Year.

Lucinda

Wednesday December 18 2013 16:19

I also shove the high shoes under my bed and ifIi go out in them Ii always bring flats lol

Niall

Thursday December 19 2013 11:37

Congrats on your introductory blog entry Aoife. Looking forward to reading more, from you, and from your wise-before-his-time son.

Joan Jordan

Thursday December 19 2013 19:14

Well done Aoife! Really enjoyed your blog. Your six year old is on the ball!

Trevis Gleason

Monday December 23 2013 09:48

Looking forward to reading more of your story of life with MS, Aoife! Well done. Cheers

Aoife Kirwan

Wednesday January 01 2014 18:02

Thank you all for the lovely comments! I'm glad you enjoyed reading it. Happy New Year!

Emer

Saturday January 04 2014 20:43

Hi Aoife,
Just been diagnosed!! Pretty scared at the minute! Don't know what to think, what to do-how to talk to my three kids!! What will the future hold! I work full time, my husband works nights - so tired I could sleep for a year xxx like you my heels have to take a back seat!! Enjoyed your blog xxx

Aoife Kirwan

Tuesday February 04 2014 21:30

Thank you all again for the lovely comments! Emer, I am sorry I didn't see your post until now. The initial diagnosis can be quite scary so I understand, but I bet your level of resilience will surprise you :) Best of luck x

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