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Member Since: May 24, 2006
Last Login: November 20, 2008
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Biography

50 years old, had mast 14 years ago, now have mets

Diagnosis

Recent Posts by lazeechic

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 20, 2008 09:51 am

Lets start a Roll Call

HI

I was dx with dcis when I was 36 in 1993.  I had a mast but surgeon did not think I needed any treatment and never saw an onc.

In 2004 I became extremely sick to my stomach, went to the hospital thinking they would say it was food poisoning only to find out I had mets in several bone sites and lung.  They told me I had 6 months to live.

- had port inserted and started on zoladex in July 2004, thing stabilized by spring 2005

- had a car accident in May 2005, broke my neck in so many places told me it would never heal because of the cancer.  Had radiation to my neck and spent 5 months laying on the floor mostly because I couldn't stand up for the pain.

-started on zoladex shots every 3 months

-saw neurologist in August said I would still never heal, had xray in November 2005 and my neck had healed.

-fall 2006 told I had cracked discs in my upper back

-Christmas 2007 told their was a large lump near my original site. Had radiation for this and the cracked discs.

-had extreme pain right from the moment I was on the table, told me it was a pain flare.

-spring 2008, constant pain still,  nurse told me my bp was very high

-went to family doc who sent me for heart tests, gave me bp meds, nitro and told me I had angina

-pain stayed, was sent to cardiologist this fall and told I had had a heart attack sometime between Dec 2007 and Spring 2008

-had xrays and have cracked hip bones

bad pain in my hips, lower back and upper back.  Had radiation fall 2008.  Very sick for a month with nausea and digestive problems from rads

having heart tests, cardiologist wants me to have an angiogram, but I don't want to do that until after xmas

last app't with onc, thinks i have maxed out on my meds and should change them.  Tumour count is about the same but pain levels are high

I think that is it, hard to remember all the darn stuff they give you lol. 

Posted in: Site News and Announcements + Comments, Suggestions, Feature Requests, Created: Oct 6, 2008 04:25 pm

Casting for Recovery Retreat

HI

I went on a casting for recovery 2 years ago in Ontario, Canada.  It was great, since then I have become an avid fly fisher, got new equipment for my birthday and have been enjoying it ever since. 

I endorse this program for anyone to attend even if you don't normally like to fish, was a wonderful experience for me

lazeechic

Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Aug 18, 2008 08:56 am

Who here is from Ontario??

HI

I live about 45 minutes north of Kingston and attend the cancer clinic there.  Does anyone on here go to Kingston?

I am stage 4, have mets to bones and lung.  I have been mostly stable (mentally well.....???? lol) for 5 years. 

Hope everyone is having a great summer

lazeechic

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Jun 5, 2008 08:51 am

Bone mets

Hi

I have had bone mets for 6 years now, do the treatments each month and have been doing fine.  I actually broke my neck (which had mets) in a car accident and it healed.  This is something the neurologists said would never happen.

The cancer leaches calcium from your bones causing hypercalcemia, this could kill you if you were not taking the treatments.  However it is very manageable for the most part.

 As well recent cat scans show many areas that have scar tissue that were once areas that had mets to them. 

No one wants to have mets, however bone ones are very treatable.

lazeechic

Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Jun 5, 2008 08:41 am

Zoladex (Goserelin), good or not?

HI I have been taking Zoladex shots for 3 years, but I get them once every 3 months.  It is a little capsule that they inject near you belly button under the skin.  There are little or no side effects with it.

They are fully covered by my insurance from work, but am not sure if they are under other plans.  They have been very effective in my case.  I have mets and have been static and a little better in some areas.

Hope this helps

lazeechic

Posted in: Support & Community Connections + Chat Room Friends, Created: Jan 21, 2008 10:32 am

CTG- messages for Scott and family

Dear Scott and family:

We grieve with you now and know you and your families love for her will remain always.

Laura's generous spirit leaves a beautiful echo in time that will resonate in our hearts forever.

Lazeechic

Angela

Posted in: Support & Community Connections + Chat Room Friends, Created: Jan 16, 2008 01:52 pm

CTG updates

Hi CTG, how are you and your family doing with all of this?  I think of you everyday and add my hopes for a positive resolution to all of your difficulties.

We have only ever met on chat and until recently I didn't know your name was Laura.  I am thinking you will always be CTG to me.

Love Lazeechic

aka Angela (so we both know our real names lol)

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Jan 8, 2008 09:10 am

November rad girls check in here!!

Re:cough

The rad doc I have told me I would develop a small cough, have a sore esophagos (spelling) with rads, which I did. He also told me that I could have a pain burst for a few days.  As well he only wants me to use baby powder on the area, no creams etc.

Reading the above posts apparently there is quite a difference between difference docs.  Makes it a bit hard for us to know what is correct.

hugs lazee

Posted in: Recovery, Renewal, & Hope + Prayers and Spiritual Inspiration, Created: Jan 7, 2008 03:30 pm

Please Pray For Ctg

Ctg, I am sorry I missed you in chat last night because I have missed you for these many weeks.  You have seldom been far my thoughts.

You have demonstrated that days are precious between those we hold close. I know your family surrounds you and you them with the circle of love .

The lovely spirit that you are will always be near to the many people you have touched.  It will float on the wave of caring that you have so generously given to us.

Love Lazee

Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Nov 29, 2007 09:33 am

My Onc would not let me do any follow up scans (ONTARIO)

One reason that oncs are starting not requesting as many scans is because data is starting to seep through about how much radiation you receive each time.  It is a lot more than x-rays. 

However Lesley if you are not comfortable with your onc I would be looking for a new one.  It is important to have faith in the people trying to help you and if you don't have that you won't be comfortable with many of their suggestions. 

I personally had a lovely chat (or arguement, depending on how you saw it) with my onc about what level of treatment, my expectations etc.  It was a very good thing because now we have an understanding of each other and it has worked very well these past 4 years.

Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Nov 29, 2007 09:24 am

we should organize a canadian get together?

HI Maybe we could organize some regional get together's, after all it is a few thousand kilometres from coast to coast. I would be happy to go to either coast but understand that it is far and expensive for most of us.

I see some ladies from south eastern ontario, would anyone be interested in getting together from this area?

Lazeechic

Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Nov 17, 2007 09:04 am

November rad girls check in here!!

HI

I found I too will be having rads this month, my left breast, left top lung and middle back.  Apparently it is growing under my reconstructed breast just over the heart.  I asked about my heart, he said he would put a"bolis" under my breast which would make sure the radiation did not affect my heart.  After reading some of these posts I now have a lot more questions to ask.  I was a bit tired the day I met him and a bit stunned as  I had not expected quite so much.  Will be thinking of all you ladies in the next weeks.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 9, 2007 09:51 am

Having a hard time with my diagnosis/ life sentence

Hi Sunny

I am now in my 4th year with mets and the 15th year with this little life lesson.

I learned  at a young age, there are no guarantees in life.  My father went to work one morning and came out of a coma 3 months later unable to walk or see.  Each day was a challenge, yet he always had a smile and a joke and a zest 4 life.

The best thing you can do is get up each day and live your life to the best of your ability.  Talk to those who can help you, stay away from the negative thinkers and don't read the stats.

Angela 

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 9, 2007 09:36 am

Metster seeking advise about a bone met

HI Wendy

I have bone mets to many areas.  I have found some relief from pain taking "taheebo tea".  You can buy it in any herbal store and it is not expensive.  I take about a quarter of cup each morning.  My fingers were getting a gnarly from the mets but it has lessened as has the pain. 

Tc Angela

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 2, 2007 02:49 pm

Scan Results In.....I'm NED

That is just wonderful news!  I cannot imagine  how happy you and your family are.  I hope you have had a huge celebration with all the good stuff like chocolate and hugs.

Angela

Posted in: Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Sep 26, 2007 09:03 am

Quitting Chemo

HI Methusala

I refused to have chemo as well but for different reasons. 

It is a very tough decision to make.  What type of symptoms were you having? 

Lazee

Aka Angela

Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Aug 16, 2007 06:40 am

Any Canadians on disability because of stage 4 bc?

HI
I am on disability with Sun lIfe, have stage 4 bc. I have had no problems. I had to apply for cpp and that offsets what I receive from Sun Life.
If you are having a problem with the carrier, then call a good lawyer, my best advice. They usually smarten up quickly
Angela
Posted in: Support & Community Connections + Chat Room Friends, Created: Aug 15, 2007 09:52 am

Sad, Sad News

Dear Olive
Such sadness for you and your family. You are in my thoughts and in my heart.

I know you have a strong faith, let it be your anchor.

Angela
Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Aug 15, 2007 09:45 am

Mone to Canada?

P.S. Misha
Just to reiterate Jeannette's point about quality of life.

Canada is not perfect, but it has a very high quality of life. We have a large middle class, apparently one of the largest and fastest growing in the world.

I would suggest you come for a visit and start reading our newspapers (globe and mail is our largest national daily), listen to cbc radio (it is broadcast internationally), these will give you some flavour of the life style.

I wish you well on this life journey.
Angela
Posted in: Support & Community Connections + Canadian Breast Cancer Survivors, Created: Aug 15, 2007 09:40 am

Mone to Canada?

HI Misha
First of all I think it would be great if you moved to Canada as you seem to be a very nice lady.

I live in Ontario and have had excellent care. The doctors would do far more scans etc. if I let them lol. Truly, when you need urgent care here you seldom wait.

You will still need to have some drug coverage though. Not all drugs are covered under the system, so if your husband has a drug plan with his work you would be in great shape.

Best of luck
Angela

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