Archive for the 'Quality Of Life' Category

Nov 06 2008

Prostate cancer treatment options

prostate cancer treatment options

4 clearly explained prostate cancer options to understand Darla’s cancer story better.

 

Since prostate cancer treatment options are getting more, the survival rate for prostate cancer also improves. This is true for prostate cancer treatments in all stages except a metastasised prostate cancer.

 

Advanced prostate cancer treatments however have no high survival rate outcome, which is sad if you have metastatic liver cancer with prostate cancer as your primary.

 

Spread is bad

 

Darla’s father however was diagnosed for primary prostate cancer in early Feb. 2008. He underwent radiation treatment for prostate cancer and except for suffering side-effects, Darla’s father is now cancer free.

 

Which only shows that you don’t want to hear that the cancer has spread or metastasised.

 

Please share all your experience and information on prostate cancer at prostate cancer symptoms. Please Darla, share your uncle’s "complete" prostate cancer story so others that will go the same path can learn from you.

 

Prostate cancer radiation treatment options

 

We add this information because it is specific for prostate cancer and helps understanding Darla’s cancer story.

 

Option 1: No prostate cancer treatment

 

An 80-year old man has the option not to treat his prostate cancer and live "happily ever after".

 

Since prostate cancer is slow-growing, especially in older men, the costs and side-effects of treating prostate cancer could be much higher than living with the cancer.

 

In this case you can hear doctors say: "he won’t die because of cancer" although he has cancer.

 

‘Quality of life’ in this case means real ‘quality’ in stead of a concept you need to try and fill in yourself.

 

Option 2: Hormone treatment prostate cancer

 

The only prostate cancer chemotherapy treatment available is a prostate cancer hormone therapy that stops testosterone production.

 

cytomid

 

These oral medicines are the so called anti-androgen drugs that will block the action of testosterone on the prostate gland like:

 

  • Bicalutamide (marketed as Casodex ®, Cosudex ®, Calutide ®, Kalumid ®)
     
  • Flutamide (marketed as Eulexin ®, Cytomid ®)
     
  • Nilutamide (marketed as Nilandron ®)

 

Young men "high on testosterone" won’t be eager to opt for this solution.

 

Option 3: Radiation treatment for prostate cancer

 

There are 2 radiation treatments for prostate cancer : internal and external.

 

  • Internal radiation therapy (brachytherapy) with radiation seeds or pellets as Darla calls them. treatment for prostate cancer
    In this one-time prostate cancer treatment pellets of radioactive material are implanted directly into the cancerous tissue.

    These seeds will kill the cancerous cells in the immediate vicinity as well as normal body cells.

    Side-effects include urinary leakage and/or penile dysfunction.

    Brachytherapy is very expensive so your doctor will only recommend this treatment when your cancer hasn’t spread yet…

     

  • External radiation therapy is the older form of radiation treatment.
    radiation therapy for prostate cancer
    You will have to go several times to hospital to undergo radiation therapy.

    Since the radiation beams penetrate through your skin, muscle and fat before reaching the cancerous tissue of the prostate, more normal body cells will be damaged compared to brachytherapy.

 

Darla’s uncle opted for the brachytherapy prostate cancer treatment where the pellets inside his body gave off radiation for the next 2 weeks after implant.

 

Darla’s aunt has stage 4 liver cancer

 

Read Darla’s family’s cancer story:

 

My uncle had prostate cancer in Feb 08 this year.

 

He went to a doctor that performed radiation therapy with some form of pellets. They were placed inside him accordingly to the size of the tumors size which was about 120 pellets.

 

After the insertions, they gave off radiation for 2 weeks.

 

Yes it was painful. He urinated a lot and got two infections that required antibiotics.

 

Then the next visit he was cancer free.

 

I hope and wish the best for all who are going through any of this. God bless you all!

 

My aunt on the other hand has stage four liver cancer.

 

I am praying for the best for her and all others going through this.

 

Darla left her comment at Metastatic liver cancer facts : secondary liver cancer

Technorati Tags: cancer story, darla, primary cancer, prostate cancer, prostate cancer options, prostate cancer treatment options

One response so far

Nov 04 2008

Stage iv colon cancer

stage iv colon cancer

Stage iv colon cancer actually means Lisa’s father is dying…

 

Please give all your hugs, love, experience and support to Lisa.

 

Stage iv colon cancer story summarized

 

Lisa’s father underwent chemotherapy for colon cancer. The colon cancer metastized to his liver and the doctors stopped administering the chemotherapy drug Erbitux.

 

Immediately the chemotherapy effects subsided and all looked well again at first.

 

Now reality struck again as the pain in his abdomen begins to worsen.

 

Read Lisa’s father’s complete colon cancer story below.

 

I need someone to help me with some words of advice.

 

Please leave a comment if you have advice for Lisa.

 

First and foremost Lisa says:

 

I am so scared as to what I’ve read online about
what lies ahead for my mother, brother and I.

 

I am sure our website doesn’t paint a pretty picture about metastatic liver cancer either. But you have to look at the whole picture: you father is leaving this planet and most likely soon after your baby will step down on this planet… Life is like it has always been: some people die and others get born…

 

Now that’s easier to say 2 years after my father died. But similar like in your life, father’s grandchild (the only one he never saw) was conceived when he was very sick (knowing the age and life situation of father’s children, that’s already a miracle on its own…).

 

So life goes on, you loose a loved one and another loved one comes back into your life.

 

Secondly:

 

Read our post: What do you say to man who is going to die .

 

Thirdly:

 

Once father was diagnosed with metastatic liver cancer, reality struck:

 

  • that life is not endless
     
  • that the end was now clearly in sight
     
  • that the end won’t be as pretty as we had dreamt about.

 

We are a family "scattered" in different countries overseas, but each year we made it a point to go back home and wished we could do that more often.

 

Well, if you have a wish, make sure you work on it in stead of just saying " I wish " .

 

Of course at this moment of your life Lisa, I am sure the pain you feel is overwhelming, and the fear of what would come is even worse.

 

But what are you afraid of exactly?

 

Fear is something that makes us not going the path we are going. I mean: if a dog suddenly get’s afraid, he would most likely run, hoping never ever to face the same scary situation again.

 

And if this is the first loved one you know with cancer, you are now like the dog. But the difference is: you have no place to run nor to hide: it’s your father and you have to get through it.

 

At last: anger!

 

Know that anger is an emotion that will show up due to the whole situation. Make sure you know it and tell others that once you get angry "for no apparent reason", it’s because your father has metastatic liver cancer.

 

Look for people who experienced cancer already

 

Others have little or no clue what happens when you or your loved one has cancer…

 

Vice versa: suddenly people that have experienced cancer will approach you and speak out.

 

I did notice that my older brother who already lost his mother in law seemed to have a much "easier" way in dealing with the entire situation.

 

For me it was the first time I had heard of metastatic liver cancer. I spend nights surfing the Internet doing cancer research about colon cleansing and liver cleansing, new cancer treatments… where my brother already told me: no need to do all that, we need to work on "quality of life".

 

Needless to say I then spend even more time on the Internet trying to define what "quality of life" really meant.

 

Quality of life

 

Finally I and my mother defined "quality of life" for father as follows:

 

  • being around
     
  • ideally no pain
     
  • live life as usual, doing the things we loved doing

 

So far for having an ideal, and then we ‘just’ needed to "make it work".

 

I read Lisa that every second of every day you want to be with your dad but can’t.

 

This is actually the hardest reality of all…

 

You just cannot spend 24h next to your father like you would love. Or so it seems…

 

This is a choice you have to make. And it doesn’t have to be 24/24…

 

Living 10.000 miles away from my father, my boss didn’t grant me an absence of leave (some countries do have understanding laws - being able to take leave in order to take care of dying family members - , my country hasn’t such laws…).

 

  • Since I have no small kids
     
  • not all our income depends on my job,
     
  • time was no more a luxury but a highly precious commodity

 

I quit my job and took a plane home.

 

We went through some tough times financially, but in the end, these are all material things and we solved them.

 

In my opinion, nothing beats the toughness father and mother went through and I am happy I could help them like they helped me the first so many years of my life.

 

Blessings in disguise

 

Good things come to those who do good…

 

Some blessings in disguise showed up after father died like:

 

  • I am now doing a job I love even more than before :-)
     
  • I am aware about cancer more than ever.
     
  • I am aware about health much more than before. I do believe that polluted air and food with pesticides weakens your body, hence make it easier for any cancer to take over.

I do admit: the price we had to pay to learn these simple facts of life was way too high.

 

But in the end, you need to try to find the good inside the bad in order to keep sane…

 

How to care for a metastatic liver cancer patient

 

Practically you need to know your strength, possibilities and weaknesses. Mom "forgot" she only has one good arm and she overused it in helping carrying father around that she torn her ligament almost completely.

 

You have to find a balance in what you can do, knowing that you can do more than you think but also knowing that you have limits.

 

Most important:

 

you need to find people to help you!

 

  • go to your health insurance and ask what they can do for you (hubby had some very aggressive arguments with the social workers of the health insurance, so be prepared to be assertive)
     
  • ask all your friends and family to help a hand and be specific in what that "help" can be:
     
    • it’s great to have somebody sleep-over for one night so you can have a ‘peaceful’ sleep for a change
       
    • if somebody does the shopping for you, you have more time to spend with your father
       
    • if somebody makes a huge pot of healthy soup, bring it over, share and eat together
       
    • if somebody has bigger feet than your father, ask a pair of their slippers, as father’s feet will most likely swell
       
  • look on the Internet for people that have been there and done that, like here. Sharing experiences does help a lot in coping or focusing, because you only get one chance here and you were all but prepared for it :-(
     
  • ask professional help and insist it’s "now or never": no point to be on a waiting list. In our case we found:
     
    • 2 visits a day from health care nurses to help with anything that normally would be done by a nurse in hospital. Washing father was surely part of it in the later stage of his metastatic liver cancer.
       
    • palliative care providing telephonic help when you call them (looks like little help, but it’s better than nothing and they did drop by twice: emotional support is priceless)
       
    • GP comes by every week and at any time of the day or night when you call him. Since father was under palliative care, the GP visits were all covered by the health insurance
       
    • "family helper" : 2 times a week 4 hours a day helping out in any work that needs to be done in and around the house and taking care of the people in the family

 

In an ideal world: you should have one person that’s 24h available for father and this person doesn’t have to do anything else than that.

 

Lisa, please leave a comment and say what you feel like saying: there is no censorship here, just that we can be late in answering.

 

Lisa’s colon cancer story

 

Commented at: One caregiver is never enough! Patrick’s father has metastatic liver cancer

 

My Dearest Friends,

 

I am going through the same as you with my father. We have been fighting the cancer for a little over two years now.

 

It was first discovered in his colon and then popped up in his liver.

 

They stopped him with his Erbitux Chemo’s over 5 months ago and since then he’s had more energy and has seemed healthy and happy and we were able to “pretend” that everything was going to be ok but still knowing in the back of our minds what was going to happen.

 

I feel as though the beginning of the end has started to happen. He’s having severe pain in his right abdomen area and is not eating as much. I am currently 6 1/2 months pregnant and am trying to be so strong for the health of my baby but am finding it to me more and more difficult as his health depreciates.

 

I am so scared as to what I’ve read online about what lies ahead for my mother, brother and I.

 

I want him to be ok again. It’s so unfair that we know what is happening to him that he is dying.

 

I’m trying to continue living my life, I have a 3 yr old, pregnant, work a full time job, have a husband and now every second of every day want to be with my dad but can’t.

 

I need someone to help me with some words of advice. Thank you.

Technorati Tags: Anger, Colon Cancer, erbitux, fear, hospice, life, Metastatic Liver Cancer, Palliative care, quality of life, stage iv colon cancer

3 responses so far

Aug 26 2008

More metastatic liver cancer minds out of control

cancer mind control

We are getting lots of cancer stories reacties sharing how the mind of a metastatic liver cancer patient runs out of control as well as his body is. Read how we were not prepared for this and read Donna’s metastatic liver cancer story of her husband "seeing things".

 

Not prepared for the mind playing tricks on father

 

We were not warned by our doctors that father would see huge spiders crawling at the end of his bed… All our GP told us was that:

 

  • we could call our GP for anything anytime it was needed
     
  • father’s pain would increase and it should be stabilized by giving more pain medicine. The side effect of these pain medicines: constipation should be monitored closely and laxatives should be given accordingly

 

The latter was already not as easy as it sounds.

 

Even given pain medication was not straight forward: what worked today most likely wouldn’t work the next day, so we had to adjust to father’s pain every new day.

 

Being prepared for all this, we were not at all prepared that father’s brain would slowly but surely start playing tricks on him.

 

Metastatic liver cancer brain deterioration symptoms

 

The first father’s mind played tricks on him was when father blogged that his liver scan should be looked at as if you were looking from top to bottom.

But in reality you should look from bottom to top (thanks to one of our readers to point this out in where is the liver located). This was 1 and a half month after he was diagnosed with metastatic liver cancer.

 

Another 1 and a half months later it was all clear for everybody that father’s mind was deteriorating. He could start cheering people up by telling a joke but halfway he couldn’t remember the end of the joke anymore.

 

One day he was rushed to hospital because he got overly scared about seeing things that were not there and he was completely disoriented. The doctor in the hospital managed to "stabilize" (as they call it) father again and he could spend the rest of his weeks at home. But even in the hospital he didn’t recognize people who came to visit him…

 

Read Donna’s metastatic liver cancer story

 

Hi, I truly feel what you are feeling.

 

My husband was told he had metastatic liver just 3 weeks ago and it has been a nightmare ever since.

 

The 3 weeks seems like 1 long day without end.

 

He has lost SO much weight!

 

I agree with the post that said it is like watching a snowman melt away in the sun (read more at Metastatic Liver Cancer Snowman Story : Start, Middle, End).

 

There have already been times when nothing he says makes any sense and he is also at times, “seeing things” that are not there.

 

The Dr basically gave him morphine and sent us home.

 

He is in good spirits and has high hopes for a full recovery…..

 

So far everything I have read and researched gives me no hope of that.

 

Liver cancer is truly a monster that sneaks up on a person. He has good days as well as bad days. He has even gone to work on a few days!

 

We have a meeting with the Dr on Wednesday to discuss chemotherapy.

 

It will be his decision whether to go this route or not. From everything I have read, it is really hopeless and will only put him in misery & make him extremely ill, with no real prolonging of his life.

 

So he will have to decide longevity OR quality?

 

This is the worst thing we have ever had to deal with. Keep praying & hoping! I wish you & your family a lot of luck & send my love.

 

Liver cancer patients are truly in God’s hands.

 

Thanks for sharing Donna, all our hugs and prayers for you and your family.

Technorati Tags: cancer mind control, cancer patient, CANCER STORIES, Liver Cancer, liver cancer story, Metastatic Liver Cancer, seconday liver cancer

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