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MRI - CAT SCAN - BONE SCAN do you need to have these

mj_weis
Posts: 28
Joined: Sep 2013

I am a bit concerned as I have completed my whole treatment, Chemo and radiation, and have never had an MRI, CAT SCAN, or BONE SCAN.  Does this seem odd?

MJ

Rague
Posts: 3255
Joined: Aug 2009

I had a CAT, MRI, bone scan and a PET (had a biopsy for a place along jaw that lit up on the PET - negative) before TX.  Had an EKG too.  Also had a new CAT on last day of Taxol as rads Dr wanted a new one before I started Rads the next week.

Winyan - The Power Within

 Susan

Lynn Smith
Posts: 1265
Joined: Mar 2011

I didn't have chemo or radiaiton and I've never had a MRI or any other tests soon after my dx. BUT my sister had 4 rounds of chemo(no radiation) and then she had a MRI.Doctor told her she was cancer free.It hadn't spread.She was Stage 2 in one breast and Stage 3 in the other breast.Double mascetomy.

I thought she would have much more treatment than she had.I mean more chemo and also radiaion.But this was her treatment.She was dx July,2012.

Lynn Smith

Double Whammy's picture
Double Whammy
Posts: 2259
Joined: Jun 2010

I used to wonder why.  I think the reason I didn't have them was because I had clear nodes, clear margins, no lymphovascular involvement,  and a relatively small tumor (9 mm).  There was no in your face reason to suspect anything that would be big enough to show up on a CT or bone scan and I had no symptoms to suggest it.  I did have a breast MRI about a year after treatments because my pcp ordered it (not oncology).  I had a palpable lump in my other breast and both mammogram and ultrasounds were clear and she said she just would not forgive herself if she didn't go one step more and order an MRI.  It was fine.  My oncologist has continued the breast MRIs on a yearly basis because now for some reason she thinks it's a good idea.  So I have mammograms in June and MRIs in December.  If I have a local recurrence, it should be caught early.  I have only blood work (CBC and comprehensive lab panel) done every 6 months and I'm not sure that any organ dysfunction caused by mets would show up until it was pretty advanced so I'm not really sure why I have them done.  Maybe they do them because of potential organ dysfunction from AIs or Tamoxifen?  Just guessing.

I used to worry why "they" weren't checking everywhere and everything on me.  I'm at peace with all that now, 3 years later because I guess I just don't want to go looking for trouble.   I feel great again but would report anything out of the ordinary no matter how trivial it seems.  I guess Im one of the folks where the risks of the scans would be greater than the risks of recurrence of the disease - and that's a good place to be.

Suzanne

 

camul's picture
camul
Posts: 2003
Joined: Dec 2010

with or right after my initial treatment. I had my first bone and pet a year after I finished in 2003. It was because I had so many side effects from the Tamoxifen. Then it was a pet or bone only when pain increased. However I did see onco ever 3 months for the first 5 years then every 6 months, and did have blood work with each of them. Iwt was about 7 1/2 years when the ct scans started and pet and bone, the pain had increased to the point where we knew something was happening, but it took another year before it showed anything, although it was suspected much sooner.
Onco didnt do routine scans, only if there were symptoms.

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