Thursday, January 04, 2007

Thursday Night NOW and THEN Friday................. AGAIN?

TREATMENT:
1 Injection Weekly;
7 Tablets a Day;
6 other medications to try and control side effects.

Blood tests every 3 weeks

The exact way in which it works is not fully understood. It is thought to have a wide range of biological effects. It may do one or more of the following:
slow down or stop cancer cells dividing reduce the ability of cancer cells to protect themselves from the immune system
strengthen the body’s immune system.


Possible side effects

People react to drugs in different ways, so it is not possible to predict who is going to have side effects or which they will have. The most common side effects are listed below:

Flu-like symptoms These include a high temperature, chills and severe muscle and joint pains.

Neck and back pain along with Migraines are frequent but manageable. (with more drugs)
They may start two to three hours after the drug is given, but may or may not last long.
Your doctor may prescribe medicine to reduce these side effects. After the first injection these symptoms may be quite severe, but they usually become much less of a problem with further injections.
Fatigue (a feeling of tiredness and having no energy)
Fatigue can be a problem and sometimes it worsens over the course of injections. It is important to allow yourself plenty of time to rest.
Feeling sick, vomiting, covulsions and loss of appetite
.
Skin irritation may occur at the injection site.(and does) This can be reduced by giving the injections in different places. Sometimes a more widespread rash can occur as a result of an allergic reaction.

Dizziness Depression and emotional changes are difficult to handle for most patients. If you feel very low while you are taking it, let your doctor know, as help is available. (more drugs)
Pins and needles in the hands and toes tremors and spasms.

Hair loss Occasionally hair may be lost. Hair loss is temporary and the hair will regrow once the treatment has finished.
Temporary reduction in the production of white blood cells by the bone marrow This reduces the number of cells in the blood and can make you more
vulnerable to infection, bleeding or bruising. It can also lead to anaemia (a lack of red blood cells). It is important to report any signs of bleeding, bruising or infection to your doctor. The bone marrow will return to normal when the treatment is stopped.
Shortness of breath and chest pain are also common.
Effects on circulation may alter the rhythm of the heart or affect your blood pressure, but this will go back to normal when the drugs are stopped.

Treatment is long and 35% of patients stop before finishing as it is difficult to follow through to the end because of the severity of side effects in most people.

Well I have had a few people ask about the side effects of my treatment this is a medical overview of what I go through. I actually have most, if not all of these effects (lucky ME)
I knew it was long,
I knew it was hard,
But..................... knowing and doing are two different things and I do get a little emotional tired and disheartened.
I do sometimes just want to stop.
But My Family and Friends make me want to continue out of LOVE.

Friday, jeez it comes round so quickly but I am here and I am ready. (Here We Go Again)


Take Care Friends. Peace and Health to all xxxxx

8 Comments:

At 11:29 pm , Anonymous Anonymous said...

i can't be bothered to sign in but you know where to find me. i'll be thinking about you ALL DAY today and sending you lots of love and hugs to get you through. i guess, if you have all the side effects, distraction is impossible...but i'll sing through the universe to you anyway.

 
At 12:39 am , Blogger Deb R said...

Sending good thoughts your way, Shaz~~~~~~

 
At 7:13 am , Anonymous Anonymous said...

Oh honey, to say that this does not sound nice...well that just does NOT do it justice. The only thing you can do is focus on the rainbow at the end of this long journey, and the health that will be returned to you. I am holding your hand from afar...picturing it now. I am also wishing for a lessoning of said very nasty side affects.

Love to you,
Jen
xoxoxo

 
At 10:41 am , Blogger Vanessa said...

This all sounds so tough but, look at you, you're enduring it so well, ready to go again... for as long as it takes.
Thank you so much for posting the links here... I just know that they will be helpful to others.
You shine like a start, Shaz.
Vxxx

 
At 1:13 pm , Blogger sandy said...

wow, Shaz...what a load of side effects to endure..but sounds like you are staying the course even when it gets hard. All the blessings in the universe to you.

love, sandy
xoxox

 
At 8:58 pm , Blogger angela said...

Oh Shaz, it sounds so awful!
But you're dealing with it with your usual grace, humour and endurance.
As Jen said keep focussed on the rainbow.
Big hugs,
Angela

 
At 11:46 pm , Anonymous Anonymous said...

sending loads of prayers and strength as you journey through all of this. hugs from poet.

 
At 1:03 pm , Blogger JP (mom) said...

Dear Sweet Shaz,

It so saddens me that you have to go through this love, but be your strong, wonderful self and stay on course. You're a fighter, even though I know some days it doesn't feel like it. But I know you'll do what you can to fight disease because you have FOUR very precious reason to be around for a long, long time! (Okay, 5 counting Ben ... and 6 counting me! cause you know we're going to be old nanas together someday!) Lots of love and healing hugs to you my sweet sista.
xoxoxoxoxo, deb

 

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