This is so so unfair. I just spent a long time writing and then editing my post and I hit publish and it disappeared!! Agh!!!! Why didn't I save!!!!!! I thought this thing had autosave.
Okay so I will try again from memory. Luckily I read it through a lot....but it just won't be the same.
Yes it is finally cool again and I am actually cold but I loathe to close the windows until the house cools down completely.
So long time no write. I was waiting to feel inspired (and didn't want to write the same stuff, treatment okay, hair still hanging in there etc) but subconsciously I was possibly avoiding it a bit because thinking and writing about chemo actually makes me feel a bit nauseous. There is a name for this: "anticipatory nausea" and I have it. I get it thinking about the chemo suite or the hospital and it hits me and I have to turn my brain off. The chemo nurse suggested a prescription for Ativan to help with it...she actually said I might want to take it if I am having a weepy day! Sounds addictive.....I haven't had any weepy days and if I get it I think I will stick to using it for chemo days only.
This last chemo day was definitely the worst yet. Had my appointment with the Onc too. Everything was a bit behind because of the holiday Monday. I was told that getting there early for my blood draw would not have helped as the early birds (read seniors) were there by 7:30am even though GRRCC doesn't open until 8am. I of course was late. So I had the blood draw (and felt nauseous starting then) and then my appointment with the oncologist. They have officially put me as a Stage III (above and below the diaphragm). The radiologist that reviewed my CTscan decided that the questionable nodes in my back were likely involved as was my Thymus gland (it was too large for someone my age...it shrinks as you age and is largest when you are 7yrs old..didn't know anything about the thymus...fascinating really). This does not change anything. The plan is still to go ahead with 6 cycles (12 treatments) which is what my oncologist had decided due to the
bulkiness of my disease (i.e. swollen face which is now mostly gone).
I had a visitor for this treatment. My friend Andrea who recently decided to quit her engineering job and go back to school for psychology, came to hang out with me and analyze my personality. We got part way through a personality test but I didn't quite make it though all 144 questions. (
Thanks Andrea for keeping me company and we have to finish so you can see if your hunches about my personality are correct!). It sure took my mind off stuff while there! I actually asked for a bucket during chemo this time (and Andrea discretely moved her brand new MAC laptop far away from me...she was showing me Vietnam photos!). Luckily I didn't need the bucket but man was it was so much more intense this time. (
BTW I have MAC envy thanks to you Andrea!). So when I got home I was starving and maybe ate a bit too much....that afternoon and evening was rougher than it has ever been (without getting into the gory details!). The next few days weren't too, too bad though. I actually made it to Avery's class trip to Yee-Haw Adventure farm on Friday and got to see climbing goats, a crazy border collie and made Avery very happy to have me there! YEE-HAW! It was a hot day and I was whooped when I got home.
So my hair.....as I said it's still hangin in there but I officially (in my opinion) need to cover my head when I go out. I have hair to cover my head and bangs (which I created a few weeks ago) and a rat-tail. Really....if I braided the long hair that is left it would look exactly like a rat-tail...not quite the look I was going for. I went to a MOE training session in Toronto for work on Monday and tried a scarf for the day. It kept slipping back a bit and I had to keep tugging and adjusting. My colleague Katherine suggested a hair band under the scarf to keep it in place...what a great idea I think it will work perfectly!! So for now I am making do with what I've got and haven't gone down the wig route yet! I feel pretty lucky to have made it almost halfway with this much hair. Next week at this time I will be half way done!
So right now I am radioactive. I had my gallium (isotope) injection yesterday and then I have the scan on Friday (2-3 hrs on my back listening to my ipod..not bad). I also have a CTscan on Monday (I just now remembered the awful stuff I have to drink for that...hope I can handle it this time). This is the progress check to see how things are doing. I should have all the results by the next time I have my appointment with the Onc on June 21st. They will do all this again after the last treatment along with a PET scan. From there they will decide whether to do radiation treatments too.
So other than that not too much happening here. We are getting busy with the girls' soccer on Saturday mornings so won't be traveling much until August. I'm planning Avery's b-day party for the end of June. She wants to have it at Bingeman's Funworx....so it's pretty easy...no room for much creativity at all though! I guess this is a good year to keep it simple :) The girls have their end of year dance show on Monday...Beauty and the Beast.
A huge thank you to Granny and Grampa Allen for making this past week possible. (
The girls miss you more, the more time they get to spend with you!!). My mum comes next week for my next treatment. The girls are certainly getting lots of grandparent attention...very nice...it's the silver lining of all this as Granny Ann has pointed out :)