Total Pageviews

Showing posts with label disease. Show all posts
Showing posts with label disease. Show all posts

Saturday, February 18, 2012

Pain, Pain Go Away

Pain, pain go away. 
Don't come back another day. 
If I cry from your wrath
Lay a tissue in my path. 


When I wake, I see my fears
Falling again covered in tears
Doctor after Doctor hear my pleas


Disease after disease is what they tell me
Fibromyalgia oh woe can it be
Chronic Pain for life shall stay
What a way to spend my day





Tuesday, January 31, 2012

Dear IBS

January 31st


Dear Irritable Bowel Syndrome,


You and I have been having this tug of war battle for a while now and I feel like I'm losing my footing. I no longer have days where I'm not chained to the bathroom. I never know from one moment to the next how much pain I'll have or if I can actually eat and keep the food down. 


I understand that you are a problem that hits world wide. I totally get that you don't have a cure and that treatment doesn't always help. My concern is that you are now taking over my life. I struggle to eat because I don't want the hassle of vomiting into the nearest toilet. 


You were not invited into my life nor were you ever really desired. You showed up, took over my body and gave me this shallow frail identity in lieu of my original strong frame. Thank you but you can take it back. 


I've sought advice from Doctors, seen countless Specialists, unending hospital visits and nights in emergency. X-rays, CT Scans, MRI`s, Blood work, you have demanded it all, yet you give nothing but grief and sorrow in return. 


Why did you choose me? What heinous crime did I commit to deserve this harsh sentence? 


I beg for mercy and reprieve.  Leave me to enjoy the rest of my years. Although, I know this request is falling on deaf ears. You are what you are: A painful, irritating disease. 


Signed in disgust 


Stomach.

Monday, October 03, 2011

Brave Face

Putting on a Brave Face

Living with Chronic Pain has presented several challenges without many rewards but the hardest challenge by far for me has been answering the dreaded question: "How are you feeling today?" I can put on a brave face and say, 'not bad'. That is the answer that can cover a lot of things without getting into many details. The problem is, 'not bad' isn't good enough for some people and they need to know more. We rate our pain on a scale 1-10 but sometimes that just doesn't work. I can be at the lower end of the scale (for me that is a 5) and feel worse then when I'm at a 10. It is all contingent on where the pain is for that time frame or if it is from a Fibromyalgia flare up.

Flare ups are the worst to quantify into a statement because no two are the same. So, I'll smile and say 'I'm okay', but really I feel like I'm going to die. Sure it's lying to a degree but I don't want the pity party that comes along with 'I'm sorry you are in so much pain'. That isn't what I need. What I need are answers as to why I am subjected to this god forsaken disease? Why isn't there a cure? Why do I need to take all this medication when all it's doing is rotting the rest of my body that was functioning properly.  Why can't I stop crying and not sleeping because the pain is so horrific that I can't get comfortable? There are so many more questions without answers that it causes so much depression as well. 

I think for me, personally, hiding the depression is the hardest thing to do. I can put on the brave face for the pain but not so much when it comes to the depression. That unfortunately, you can see in my eyes. That is something you just cannot hide. People can see the sorrow in my eyes, the tears that have been shed repeatedly because of not being able to stand the pain. I was never really a 'winter' season athlete, so the winter is not as depressing activity wise. During the summer, however, the depression is much worse. I was very active. I loved to dance, swim, play tennis, play baseball or just to walk on the beach for hours. That is the hardest for me. I live so close to the ocean that it pretty much kills me inside knowing that I can't walk the 'Seawall' like everyone else in Vancouver. Hell it pains me that most days I can't even walk to get the mail (which is in a box 2 houses over). 

One of most frequent places I put on a brave face is in the kitchen. I love to cook and bake. Being able to roll dough, fondant or even just stand to peel veggies or prepare a meal is virtually impossible without having to take several breaks now. I loved throwing dinner parties and preparing elaborate meals for special occasions and holidays, now it's a trial just to make a daily meal. But I'll smile and not say a word to anyone except my husband. I've given up trying to really hide my pain from him. As he knows me better than anyone how much pain I'm really in from day-to-day. Sometimes, that is even minute-to-minute.  After multiple visits to the hospital because the pain has been unbearable, I'm fairly certain he can read through the facade and see my soul slowly dying inside. 

I guess what it boils down to is that I really dislike being asked how I am feeling and would rather have someone ask 'What can I do to make your day go a little easier?' or better still 'How would you like to cry on my shoulder for a while?'. A good cry is sometimes better than a doctor visit. It doesn't help the pain but it does ease the sorrow off my chest even if it is only temporary.

My brave face will be there right until they bury me or so I hope.