Struggling through Chemo

Hi Gorgys, yes I have the injection 24 hours after. No side effects for me so far and I've had 3. 

Today is my fifth day of the first AC session of the total four. Not bad but feeling very tired. As you all, we just want to go through this journey with all ups and downs like all the amazing women in this network. I hope too that the paclitaxel will be easier on my body. What really helps me is the rest, eating small meals frequently and drinking water.  I also do not want my family to worry, so I am really trying to listen to my body and try to recover for the next chemo infusion. Just wondering if any of you are on Pegfilgrastim PEG) injection, and if so , did you have any side effects? I have not although I was told to expect chills and joint pain. 

Hi, 

First time replying or posting anything here! 

I feel like I could have written your post! I am however  behind you in timeline. Had a mastectomy, node clearance and recon on 14 December and started chemo last week (fortnightly AC x4, then weekly for 12 weeks). 

I just wanted to reach out and say hi and you are not alone.

I coped amazingly with surgery but fear chemo will be a bumpy ride (it already has been). I am also struggling emotionally as well. Before all this happened, I had a trip to Hawaii booked and would have been leaving Sunday. Wow how life has changed. 

I also get having a great support system that can't possibly understand how this all feels,. I can't imagine doing all this without them, but they get to have a break from my hell hole while I have to live with it everyday. I feel guilt that I make them worry too. 

Anyway, I know I have not helped, but what I take comfort from is that many sisters have been in our shoes before and have made it through. I refuse to let this be anything more than a chapter in my otherwise fantastic life book. 

Hello Rona, I've done 3 of 4 AC then on to 12 rounds of paclitaxel, then radiation. I'm lucky too to have a good support group around me, and my side effects have been relatively mild, but the fatigue floors me the first week after treatment. I flop about for about a week, before getting a 'good' week where I feel almost normal, catch up with a few people for hot chocolate (coffee now tastes musty) venture into the supermarket, just to get out of the house. Then into the next round. I'm hoping I might have a bit more energy with the paclitaxel, and maybe work from home a few days a week. Some days it feel like a very long road, but I keep telling myself it's for all for the greater good, and look forward to the beginning of June when the chemo side of things should be done. Katie