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Everyday people on chemo

posted Monday, 16 November 2009

Slowly up from sleeplessness

The day started quite slowly for me, I did not sleep that much overnight, so it was dawn before the winks really set in.

But then, one wanted to wait up for the 07:00AM drug intake but slept past that time to just after 09:00AM. Naughty!

Soon afterwards the neighbourhood nurse arrive just before eleven to dress my foot which he now felt was looking a lot better, even I was not feeling as much pain, partly due to the absence of most of that necrotic tissue and the new pain medication.

When I finally got out of bed, I had enough time for breakfast then decided to take my own flask of Smoky Earl Grey tea, sugar, milk and my own mug – sometimes, what you want to be just so has to be made so by what you do yourself rather than rely on others to do.

A full house it seems

My friend had offered to escort me to hospital, which gave a very welcome feeling, especially if one were to feel a bit weary after treatment.

We took the public transport route and we were there in just 17 minutes and were 5 minutes in time for the 14:00 appointment.

Gosh! The out-patient chemotherapy room was a full house, all seats were occupied such that I was asked to wait about 5 minutes – I pretended to swoon which made everyone laugh or giggle at my antics – a pleasant way to say hello to everyone.

I took an ordinary seat and waited, browsing through my Economist magazine without much concern for whatever else was going on.

In just about 10 minutes a seat was vacated, cleaned up and available for me to use, I got in and before I had the needles stuck in, I had poured myself a cup of tea and had sipped half the cup.

Needles in everyday people

Looking around everyone in the room, they were everyday people, not many that much older than I was and hardly anyone looked sickly or incapacitated – we had all come from some place for this treatment that lasts probably an hour or two and then we would return to our abodes like ordinary people. Nobody had an “I am on chemo” sign stuck on them; they would have had to say so to be identified.

I usually like to have the needles stuck in my left arm and I look away towards to the right, since I am right-handed, it is good to have the right hand free for a pen on Sudoku. However, when I was in for the bloods last week the nurse insisted on using my right arm when I offered my left, so this time, much as I preferred the left arm, I allowed it to go in my right arm.

The saline drip was first attached then after confirming my date of birth which I hesitated to recall the Caelyx medication was attached, apparently, I am the only one with my kind of treatment, wrapped up in aluminium foil and timed to finish in an hour.

Infusing or extracting

In fact, not everyone was being fed intravenously, there were others having fluids drained out of them from either the chest or the abdomen, I did not find out if that was a kind of venesection, but the lady beside me gave up a good 6 litres of fluid which immediately went into the special bin, so none of that was for analysis.

As the hour passed, I had downed 3 cups of tea and had a wafer donated by one of the out-patients then the intravenous drip system beeped that it was running out of Caelyx, the system was then adjusted to flush the rest of Caelyx through the tubes into my system – that was easy to observe because Caelyx has a reddish colour.

Metal access but plastic endures

When it was all clear, the needle was removed and I was surprised to see that the insertion process was with a metal needle but that was retracted at the start to leave a plastic needle in the vein, then I understood why it looked flexible towards the end of the treatment – I must say there is a lot of ergonomical development on medicine delivery systems.

Soon, we were ready to leave, I felt strong enough to brave the public transport system and it was interesting to see this young man literally run into me trying to get on the tram first without due consideration of someone with crutches – when I remonstrated with a loud, “Excuse me” he caught himself and said sorry.

Getting home was without much event and that was my third course of chemotherapy completed.

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1. Uzo left...
Friday, 20 November 2009 9:02 am

Akin, I pray you get better soon. God be with you always.


2. Akin Akintayo left...
Friday, 20 November 2009 12:01 pm :: http://akin.blog-city.com/

Hello Uzo,

Thanks and God bless you,

Akin


3. Ate left...
Wednesday, 25 November 2009 8:31 pm

Akin, i wish you a swift recovery, and my offer for help is still valid of course ;)


4. Akin Akintayo left...
Friday, 27 November 2009 12:11 am :: http://akin.blog-city.com/

Hello Ate,

Thank you very much, I would invite you over soon. I am very grateful for your offer.

With the kindest regards,

Akin


5. Olaoluwatomi left...
Monday, 30 November 2009 5:39 am :: http://www.olaoluwatomi.blogspot.com

All the very best!


6. Akin Akintayo left...
Wednesday, 2 December 2009 9:48 am :: http://akin.blog-city.com/

Hello Oluwatomiwa,

Thank you very much.

Thanks!

Akin


Tag Related Posts

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Friday, 5 February 2010
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Wednesday, 20 January 2010
Not being afraid or embarrassed to tell my doctor everything about how I feel has meant my medication being adapted for my feeling better.

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Monday, 18 January 2010
Attending my 6th chemotherapy session and my confusion between left and right.

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Friday, 15 January 2010
The Friday before my 6th chemotherapy session, I was out to see the oncologist, the nurse and the priest.

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Wednesday, 30 December 2009
Emetics, emesis, anti-emetics and the feelings best left unspoken.

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Monday, 28 December 2009
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Saturday, 26 December 2009
The logic was since I tolerated the chemotherapy I could have more, not less. I suppose that means another 4 sessions of chemical infusion.

He walks the earth in our shoes

Wednesday, 16 December 2009
My third visit to hospital this December brings medically sanctioned good news about the condition of my foot and what next to do.

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Looking at my foot today, we came to the conclusion that it had healed in a relatively short time it could be classed as a miracle of healing.

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Monday, 7 December 2009
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Nigeria: A motion to pray is rejected

Wednesday, 2 December 2009
A Nigerian senator had his motion to pray for the health of the President rejected. The issue is no so much the rejection but issues of health, healthcare, understanding prayer, public office, public service and the shame of not having hospitals.

Nigeria: Yar'adua's health, a truth but not the whole truth

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What we learnt of President Yar'adua's health this week is a new truth but it is hardly the whole truth about his health and what we have been made to believe all this time.

He could have dispelled those rumours but chose to put out a decoy.

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Wednesday, 25 November 2009
I have had 4 different kinds of dressings applied to wounds as medical treatment has dictated what is suitable for each stage of healing.

Everyday people on chemo

Monday, 16 November 2009
My third course of chemotherapy reveals much about people and the comforting thoughts that go into medicine delivery systems.

Stronger medicine and another course of chemo

Monday, 16 November 2009
My visit to the hospital in Friday brought on a few more things, stronger medicine for the pain, another course of chemotherapy, the snipping away of necrotic skin at surgery and another X-ray of my foot.

My left foot

Thursday, 12 November 2009
I was in hospital today to give blood for tests and collect my much maligned orthopaedic which now turns out to be a bespoke work of beautiful workmanship.

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Friday, 6 November 2009
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To live in one shoe

Wednesday, 4 November 2009
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A primer on cancer and chemotherapy

Monday, 26 October 2009
A basic primer on cancer and chemotherapy to help understand what it is and how it is treated.

A second course of chemotherapy

Monday, 26 October 2009
Took a second course of chemotherapy and had the wounds nurse check the lesions.

It's more chemo on Monday

Friday, 23 October 2009
My hospital appointment with oncology today signified I needed to take another course of chemotherapy on Monday. Bit disappointed but I would do well. My toes however attracted much interest from many departments.

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Wednesday, 21 October 2009
From getting around with crutches and a bicycle to bloods for analysis, another time to thank the nurses and the priest to using laughter to kill the pain. Another day of useful lessons.

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Saturday, 17 October 2009
Within my professional comfort zone, I viewed bedpans in derogatory language bordering on disgust until I found out through experience in hospital that doing bedpans was essential to my recovery.

The nurses @ OLVG have my deepest gratitude.

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The commandment to Love Thy Neighbour as Thyself is a safety regulation regardless of belief for you, not an exhausting drill

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Thursday, 15 October 2009
Other observations of hospital hierarchies and deep knowledge of your situation.

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Thursday, 15 October 2009
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After my 1st day back

Saturday, 10 October 2009
My first day back home went very well, I'm happy.

Home - At last

Friday, 9 October 2009
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One more night

Thursday, 8 October 2009
I hope to leave hospital on Friday subject to a few home help arrangements.

I'm alive after my autopsy

Tuesday, 6 October 2009
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Monday, 5 October 2009
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Monday, 5 October 2009
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A slumbering machine operator

Saturday, 3 October 2009
Sleep and food with introductions to others.

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Saturday, 3 October 2009
Nausea is brought under control with suppositories but the day passes by with me under most of the time.