Friday, February 5, 2010

Nasty Side Effects

So, it has been interesting the last few weeks with the chemo drug. It and I just aren’t seeing eye to eye! It has been giving me lots of side effects and at times they are quite painful. The hands have been red, hot and swollen. The finger tips will feel almost rubbery at times and then at other times they are very cold and will have a pale blue hue! Nausea has been quite nasty, sometimes the meds work and sometimes they don’t. The feet have been picked on the most by the drugs. Very tender heels and the balls of the feet. And blisters – holy crap! Remember when you got new thongs (flip fops for the younger generation) and you always got a blister on your foot. Well one maybe would be ok – but had 4 and 5 on each foot – between the toes! Ouch. And the temptation to break the blister was so there, but I was good and left them alone!

Phoned the nursing line three times – which I have never done, and the nurses are so good and of course they are ones that I have had in the chemo room. Had Trace on Thursday and he said not to take the evening pill and if still felt the same way on Friday, not to take the morning pill and phone into the nursing line. He also said to stay off my feet as much as possible and to not do dishes – now that one I liked!! I did have to call, and got Shelley – she listened to what I had to say, and said she would go and talk to Gary and call me right back. Oh I would say less than 4 minutes before she called me back – Gary had said to go off the drugs and would see me in a week anyways. Gary had said that once the side effects started to affect my daily life, then off the meds. Monday phoned in again and got Phil and he said just take care of the feet and the hands.

Friday was blood work day and a visit to see Dr. P. Brian and Patrick were both with me. The gals in the Medical Day Care are great – funny and caring. Though had one nurse who was from Royal Columbian and I swear she was an older Heidi – hair pulled into two buns on each side of her head!! Gained 1 kilo – I wasn’t too happy with that – most women will agree with that – we like the scale to go down not up! Gary said my numbers were good – within range – though my tumour markers were up to 257 – and he didn’t seem to be overly concerned, but it will get watched for sure. He asked how I had been since going off the meds a week ago. Said it had gotten worse (which I was told by Shelley) and that the feet were very sore as were the hands. He checked out both. I told him that I was not happy with the drug at all. He said I could quit I right now or try and see what it would be like at ¾ strength. I would be taking 6 pills a day rather than 8. He also said I had the CT scan coming up and then we would see if there was any shrinkage in the tumours. If not, then possibly do another drug cocktail. Patrick asked him about my memory loss – lovely child!!! I said chemo brain. And Gary agreed – they don’t know why chemo brain happens. And Brian mentioned my light headiness. Gary asked how often it happened and how long it took for it to go away. Another thing to keep an eye on. I had good heart and lung sounds – I like that. He gave me a new Rx for anti-nauseau and I have had them before.

I am having the bone scan on Tuesday and asked him if I was going to have to wait 3 weeks (that is when I see him next) to get the results. He said that those scan results take a little longer, but I could call him on Friday or Monday and ask to speak with him. He said he would call me back with the results. Which will be just fine, thank you very much! I am a little impatient when it comes to getting results!

Went out to the waiting area as we always do, when one of the chemo nurses, Olivia, came over and sat and talked with me about calling the nursing line, just some tips on handling the hands and feet. Then she went away and then came back again – said that Gary was only giving me 10 days worth of the meds and that someone from the nursing line would be checking up on me – so getting a weekly call from them. Then out comes Gary – this never happens!! Just backing up what Olivia had said. Went and got my meds from the pharmacy and will see Gary on March 1st.

Went to my Women with Metastatic cancers group session on Wednesday. It was pretty upbeat for the most part, had a new gal join us which is nice to see. Some of the other women who hadn’t been for a bit were there and we had a lot of laughs this week and less tears. We may cancel the next meeting as it is during the Olympics and well, it will be chaotic around the cancer clinic!

Had fun working in my garden in the front the other day. Meghan and her kids were over. So Ryan who is 2 ½ helped us too! I moved him to the other side of the garden and gave him a little shovel and he moved dirt around! Managed to plant bulbs in two large planters (with the much needed help of Brian!). Meghan is good at working in the garden – so she cleared out a good amount of the weeds that had sprung up with our spring-like weather. And we planted a bunch more bulbs. These were bulbs that should have been planted in the fall. Oh well, better late than never!! Once I finish this blog, shall go out again – it is a beautiful spring day here – yeah, I know it is still winter, but tell Mother Nature that.

Seeing as Patrick will be leaving soon for basic training, we had a “Mug-Out” for him at one of the local pubs!!! He had a great time, though I think his head hurts just a little today!! Brian presented him with a boson’s whistle – which he will so get used to hearing once he is onboard one of the ships. And of course no one took pictures of this and there were a few cameras around. Everyone had a great time – think there were about 25 people there – we took over the entire patio at one point! Was nice seeing some of the kids he went to school with, his cadets friends, relay friends, family friends and most importantly, family – Shannon and Meghan were both there. His swearing-in ceremony is on the 11th and he flies out on the 20th. Will be quite in the house with him gone.

Think that is about it. No – that is not all! Brian is officially a Commissionaire – looked quite dapper in his uniform when they took his picture for his licence. So may not see much of him during the Olympics – with him working and me volunteering as well.

The Olympics start on Friday and everyone is getting excited – we just want some more snow on the local mountains! And our Canadian athletes are going to do Canada proud and bring home some gold!

That is all for now. Next posting will be March 1st unless there is something thing oddball with the bone scan and don’t think there will be anything. And will tell you about my volunteer stuff that I will be doing during the Olympics – it is going to be fun!!

Go Canada Go!!!!

6 comments:

Anonymous said...

Wow! You are a busy lady, sorry to hear about those side effects, that is very hard. Glad you have a great support group and such a great family, Roni. I can't believe you can garden already, that sounds so nice. My son is going to the Olympics , have a blast volunteering there, congrats to Brian on job. Take care Roni, as always you inspire me. Sandra Erickson.

Anonymous said...

Hi Roni, Glad to hear your numbers are making the doctor happy... (even the weight gain) I am praying the bone scan results are also good. You have stood up well to the side effects and I know it must be awful. I could not imagine blisters between my toes and I have only ever had one at a time on one foot... how you ever resisted popping them is beyond me. Sounds like Patrick;s send off was a good time.. sorry I missed it. I have signed up for the Country Dancing Boobies Relay for Life again, and have started my fund raising efforts. While I am volunteering at the Olympics I am knitting chemo caps, and I hope to have a dozen finished by the end of the games. Would love you to come with me to drop them off at the Cancer clinic. Isn't our weather fantastic? I love that you are getting a head start on your gardening, should mean some more fabulous pictures this year..... Enjoy your olympic festivities, and we will catch up after the games..... Love ya Rae xo

Anonymous said...

Never mind Canada - GO RONI GO!!!

Stay strong Angel friend. I celebrated 5 years cancer free on January 7 and thought of you. Did you enjoy our toast?? LOL It was an extremely smooth glass of my very favorite: Wolf Blass Premium Special Shiraz. Interestingly enough is was a 2005 - Special indeed given that's the year I finished my last treatment.

Getting xrays for pains in my back but am hopeful it will be merely to give me peace of mind. Have a great February but don't run yourself down girl.

Will be down your way for the same conference I went to last May so am hoping we are able to do a repeat of our lovely afternoon coffee date we had last year. :-) Hugs, love, and laughter, Bonnie

Anonymous said...

Hey Mzzzz Veronica!

I hope they figure out a better "Pill" for you soon. You are one hellacious & tough cookie, and I give you all the kudos in the world girlfriend!

About those "thongs!" I remember vividly the blisters new "thongs" would make between my toes. I hurt for days after it popped!:O( By the way, about the word "thongs." Theresa, Margy and I went to a sports pub after Steven's memorial. We were sitting around talking and for whatever the reason was, I mentioned "thongs" as in flip flops and Theresa said, "Yah, tried them once and they were so uncomfortable, especially how they ride up you, I never wore them again," and she made that face like only Theresa can, and Margy and I just about fell out we laughed so hard. It was too funny! They call them flip flops in the states too, which I thought strange when I first moved here, but now...we have to explain what they are unless we are talking to the 50+ club!:O)

Wow...the Olympics are around the corner aren't there! I don't plan to come up since I do not want to deal with the border, nor the traffic. I hope it goes well for Vancouver though. The city is known all over the world right now...which could be good or bad...it has changed so much since we were younger. When I go home at times, I feel like I am in a different city. But then, they don't call it beautiful BC for nothing!

I wish Patrick all the best in his new career. I know you will miss your baby boy, but the good side of it is, he will be stationed near home. That is a good thing!!
I hope you have a great time volunteering at the Olympics...you will be sharing in a part of history..that is very cool!

You must have a lot of faith in the weather planting for spring...I just don't trust our "flip flop" Ha, Ha...weather. Snow in April...why not. My sister/father-in-law live in DC and Maryland and are experiencing the 30 inches of snow right now. The city is pretty much shut down. Better them than us, we had our share last year!

Looking forward to hearing about your experiences during the Olympics. Go CANADA!!!

Love you...Talk soon

Eileen

Roni said...

Sandra - does that mean you get your grandson while Mike is away? We had 14c here today - spring weather - but we want snow!

Rae - we have to get together after the Olympics - we will both be busy during them. I get my orientation for Molson Canadian Hockey House tomorrow and our uniforms. Will be fun!

Bonnie - heard you had a vistor the other day!!! Glad Ardene got to spend time with you. WOW 5 years already - that is great. And that means we have been friends and angels for 5 years too - hope your xray is nothing but a strain or something. And have them take one of you standing up - shows things that laying down doesn't! Found that one out years ago!!

Eileen - I can just see Theresa and the look on her face!!! And I would't try the border till the Olympics - though your Mum will miss having you up for a visit! Patrick will only be based in Esquimalt for a year once he finishes his basic - then he could be posted to Halifax or Esquimalt - either way - still close enough to come home. Think that he and I will have a good time at his graduation - he wants to spend some time in Toronto as well.

Niki G said...

Busy as a bee I see. Thanks for the updates. Hope the side effects dissipate and let the drugs do what they are supposed to do! Have fun with your volunteering. I'm sure you'll have many stories to tell!!