Showing posts with label MIBG Scan. update. Show all posts
Showing posts with label MIBG Scan. update. Show all posts

Friday, 30 May 2014

Update

Hi everyone,

Sorry I haven't updated in a while, but I haven't heard anything either. Finally, being fed up of waiting, I started to consistently call Dr. Nicholas's office and finally heard back from him this afternoon. Apparently, he forgot about me because he never heard anything from Toronto and Toronto forgot about me completely. So Toronto took my file to the rounds meeting this morning. A rounds meeting is where all the oncologists sit together and discuss their patients with all the doctors (especially special cases like mine where they aren't sure what to do). So they discussed me at the rounds meeting today and all the surgeons agreed that I would be worse off after surgery at this point because at this point the tumor is still attached to the spinal cord and some nerves. They need the tumor to be smaller to feel comfortable with surgery.

So this is what they decided on, bear with me because it's hard to explain. They didn't give me the name of the procedure, but I will explain it as Dr. Nicholas explained it to me.
There is a special scan for neuroblastoma patients called an MIBG scan. Before the scan, I get a special radioactive injection (the initials of the chemicals are MIBG). Anyway, the chemicals are attracted to the neuroblastoma cells and light them up for the scan. This procedure which is new to Canada and ony available in Toronto (not Ottawa) is the same kind of chemical but stronger and is given through IV. It's supposed to attack the cancer cells and hopefully drink the tumor. (Wouldn't that be lovely). Therefore, I have to go to Toronto twice this summer. First time is one day for an assessment to make sure I qualify, which I obviously will but the doctors also want to see me in person and explain the procedure better. Second trip, I will get the iv infusion an then have to stay in the hospital for 5 days as I will be highly radioactive and am not allowed out in the general public. I will be in a special room with a special X-ray wall so that visitors won't get radiation from me. It will be hard for me because I hate being away from my family, especially the kids and it will be boring because I can't even go outside for walks etc etc. I will post more when I know more and when the appointments are booked.

In other news, Liam's starting to perk up from his pneumonia and we are moving to Cornwall on July 5th to a beautiful one floor bungalow house with a big yard.  It will be a new and fresh (well-needed) start.

Thanks everyone
Priscilla.

Elizabeth had some fun in the mean-time



Monday, 5 November 2012

Latest News

Hi everyone,

I know this post is long overdue and sorry for making everyone wait..

- After the last Toronto trip, things were supposed to proceed quickly, but unfortunately they didn't. My case has a new person working on it now. A doctor from Sick Kids Hospital in Toronto who is a neuroblastoma expert. I can't remember his name at the moment???  He looked over my images and believed that the tumor may have been dead!!!!!!! I was scheduled to get an MIBG scan. Because of the rarity of this scan it did not get scheduled until the end of October as they need at least 4 people scheduled to do the scan. What a stressful 2 months that was!!!!!!

Got the results of the scan today. The tumor is not dead :( BUT.... It is less alive then it was originally!!!!!!!! To me that is great news, Even though the chemo and radiation did not shrink it, it did diminish the active cancer cells :)  I a not sure where this brings us for next steps, but I am happy that we are going in the right direction.

Now we wait again. Dr. Nicholas will send the results of the scans as well as the images to Toronto and we wait from there. I am planning on enjoying my holidays happily knowing that I am slowly, but surely beating this :)

Hope everyone has great soon to be holidays and I will update when I know more.. Thank you

Priscilla

P.S. The smoking battle has not been won yet.. But I am getting there. Slowly but surely.. It is a hard battle