Hi! My name is Clive, and I have cancer ...

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Hi! My name is Clive, and I have cancer ...

Postby Big C 69 » Fri Nov 28, 2008 2:40 am

I was diagnosed with cancer on 27 November 2007 after I had a 'Bad Mole' excised from the left side of my chest (situated on my 5th rib). My Oncologist staged me as Stage IIIC.
I had had my mole for about seven years, and it had been ulcerated for almost five years.
I immediately underwent a 'wide excision' of the infected area, and had a lymph node biopsy (under my left arm). Five lymph nodes were harvested, of which one was infected.
Four weeks later I had completed lymph node removal in which another eleven lymph nodes were harvested, and five were infected.
My Oncologist urged me to undergo chemotherapy (1 month of high dosage Interferon; then 1 year low dosage Interferon) but I had to decline the treatment because I suffer from Muscular Atrophy (Charcot-Marie Tooth Syndrome) and, although I can still walk (barely), I know for a fact that my body would not handle the side affects of the potent drug.
About two months ago I had some CT scans done of my head, neck, chest, abdomen and pelvis. The CT scans showed no visible tumors, but they did reveal that I had emphysema in my lungs, and Hydrocephalus (water on the brain) which is why I insisted on having CT scans of my brain because of excruiciating headaches.
I was referred to a Neurosurgeon who told me that my Hydrocephalus was already at a dangerous level and that I could suffer a stroke or even brain damage. But he said that there was no evidence of a tumor causing the blockage. I will only have a shunt inserted if my headaches last for longer than two days, or if I vomit while I have a headache. Thanfully this has not yet happened!
I am already feeling excruiciating pain in my kidneys and have problems passing wind (flatulance). Two weeks ago I found a lot of blood in my stool ('shit') which was a terrifying experience. It was the second time I've discoverede this, the first time was on 7 April 2008 and had no recurrence until two weeks ago. Now I am terrified of going to the toilet in case I see this again. (I somehow know that the cancer has infectede my colon.) I have not told anyone about this, not even my Oncologist. I am not married but I do have a wonderful loving family and the best friends a lifetime can buy. I have decided to keep my 'blood in stool' discovery silent for now, as I don't want to worry them more than they already are.
My medication includes; Doxyfene S5 (for pain); DF118 S6 (for pain); 500ml of Morphine Syrup (10mg) S7 (for pain) and Propranolol 40mg (to control my shaking caused by Muscular Atrophy).
It has been a rollercoaster ride into hell, but I am determined to see my 40th birthday next year. If I can achieve this, then I will have one of the most memorable birthday parties ever because my birthay is on 31 December.

If anyone would like to contact me, my Email address is: clivegasco@live.co.za
Big C 69
 
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Postby Pip » Fri Nov 28, 2008 9:26 am

Dear Clive.
I am stunned and unable to write anything here but will email you when I can.
My God.....You poor man. To be writing at some unearthly hour you must be feeling very low.You must get help and the people on this forum are better than I for 'words' of advice on this.
best of luck.
I am shellshocked.
Pip
 
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Joined: Sun Nov 16, 2008 5:07 pm

Hi Clive

Postby seanty » Fri Nov 28, 2008 12:35 pm

Hi Clive,

you have posted on the member's polls section, where not everyone looks. You will have more responses on the general info on melanoma section here: http://www.scansol.co.uk/forum/viewforum.php?f=1

It sounds like you have been in the wars.

S
Seánty
--------------------------------------
www.mymalignantmelanoma.com
seanty
 
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Location: Derbyshire

Postby tewy72 » Fri Nov 28, 2008 12:56 pm

Clive,
Just wanted to let you know that I've read your post - really sorry to hear your news.
As Seanty said a lot of people will be along to offer support when they read your post.
It sounds like you have come through so much - please try and mention the blood in your stool to someone, it may be unrelated and you could be stressing unnessecarily. Get all the help and advice you can :(
Thinking of you
Kathy
tewy72
 
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Location: Melton Mowbray, Leicestershire

Re: Hi! My name is Clive, and I have cancer ...

Postby MaryOf » Wed Jan 13, 2010 10:47 am

Clive, I am so sorry to hear what a terrible time you are having and as I was reading through your post, I assumed you were much older than you are. I am in no position to give you advice, as I can only comprehend what you are going through....Having said that, don't you think you are in a place where you should be putting your needs first without having to take on the responsibility of how other people will worry. I would bet they would be very upset to think you were carrying this alone. I will certainly be thinking about you on your 40th birthday.
MaryOf
 
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