Sicky Sickness :(

Oh I'm a moaning Michael again! I have tonsillitus but have also picked up some virus as well. I feel very "bunged up" in my head so am less than constructive right now. I've gotten better at taking my vitamins too though, so maybe this is illness will get me into a better habit. I take Naudicelle Plus, which is a mixture of Vitamin D and Evening Primrose Oil. I started taking these tablets just after my diagnosis so I can't say whether they work or not, but it can't hurt to take them... even if they are the size of my thumb and I have to take six a day!!!!!

I've had a bit of a tough couple of weeks emotionally too. Just as I feel an improvement in my mood, I hit a brick wall again. It got me thinking about Elisabeth Kubler- Ross' Five Stages of Grief. I remember studying this in college in the actual context of grief during a terminal illness or after a bereavement, but it can absolutely translate to grief after being diagnosed with an illness like Multiple Sclerosis, as you are grieving for the life you had before diagnosis.



As you can see from the illustration, the stages are denial, anger, depression, bargaining and acceptance.
They are not the exact emotions that everyone will feel, but more of a framework to help us understand what we may be feeling at any given time in our grief.
These stages are said to be experienced at different times by people experiencing grief, and are not reached in any specific order.

I can definitly see where I've experienced specific emotions from the Five Stages, and I can also see which ones I struggle with and keep coming back to. I don't know if the "Acceptance" stage is easily reached, but I'm going to allow myself to reach them it my own pace and not feel that I need to be okay with this diagnosis now. After all, I am still a newborn in this MS journey.

1 comment:

  1. I do hope you start to feel better soon! beautiful header picture by the way and beautiful name for your blog! I like originality and this is certainly it!

    I found your blog when searching for similar blogs to my aunties and thought you might be interested in taking a look. It is called Bette Bravo (named after their dog) and it has information and lifestyle tips about MS and the new CCSVI treatment available

    She lives in Norwich, England and suffers from Primary Progressive MS. She has had it for a good few years now but as a child i didnt really notice, it is only as i have got older that i realised she was suffering - she always seems to have a smile on her face, which humbled me with her braveness! You reminded me of her! She is currently waiting for the treatment CCSVI in Poland - apparently it is not available in the UK yet but if tests are positive they may roll it out here.

    As she says, this could be the beginning of a cure for this disease.

    We have every finger and toe crossed for improvement! She is having the operation in August and she is uploading a lot of videos to show her condition before and after the op. She is rather technically impaired hence why I am contacting you, but she would love to hear from you and your experiences and if you would like to know more about CCSVI please please get in contact.


    Kind regards and best wishes

    Kate

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