18 Replies Last post: 03-Apr-2010 07:34 by carold   Go to original post 1 2 Previous Next
Click to view boobyprize's profile
hey, i am into my 4th year of havin b/cancer, i remember havin chemo, an i was knackered, hated the procces, but soon found mr hickman, an that was a godsend, its not talked about much, but really should be, but all in all, we all get through it, you just have to,.
Click to view Poshspice's profile

Hi everyone

Chemotherapy, well it has certainly slowed me down. I am on carboplatin / taxol in 3 weekly infusions and have just had # 5 with one more to go. I have to sit in the chemo clinic for 6 - 10 hours (depending on how quickly the pharmacy makes it up) with a cannula in the back of my hand. I have really prominant veins but for some strange reason the nurses often have problems inserting the cannula. I had a leakage with a bit of thr chemo leaking under the skin and also get bruises afterward.

The effects of the chemo on me are pure fatigue. Each one has been acculatative (think I spelt that wrong!!) so the fatigue and tired gets worse. In fact it is a week since my last treatment & I am still in bed. I have decided to give into the fatigue (can't fight it to be sure) and just REST and REST. The following 2 weeks will be much better and I will be back to normal.

I do find the steriods a problem - particularly with sleeping as they keep me so alert. I have weakened and my GP has given me sleeping tables as I used to lie awake until 4.00am most nights. Taste - yes for the first week after chemo everything tastes awful. But the knowledge that this is go in week 2 & 3 makes it bearable. I have only JUST noticed a slight tingle in my feet - like "pins and needles" but because I know it is a side effect - I can deal with it. I do also feel slightly nauseous but eating normally deals with that. Oh yes i have put on ABOUT A STONE in weight which bothers me - but hey just one minor inconvience. And finally I have lost ALL of my hair on my body! The lost of my eye brows and eye lashes are the hardest to come to terms with because it makes your face look so strange & add to making you look ill.

Sorry if this has been long winded but hope it helps someone who is feeling afraid of chemo - its not that bad!!

Tina

Click to view canasta's profile

It is really interesting as a daughter of cancer patient to read how you all coped during your treatment. I am finding it difficult to understand what mum is coping with as she won't tell anyone how she feels, just says she is feeling rough!

As I live 170 miles away and contact is by email as she can't talk on the phone due to her cough, I worry all the time about how she really is coping especially on her own- her choice.

She says she hasn't lost her hair but we think she may have a wig on- hair used to be short and curly , now longer and straighter and higher on forehead.

She looks so grey and thin in the face, has a distinct hospital smell around her. she is on gemcarbo for lung cancer. gemcitabine and carboplatin.

Has anyone any experience of this type to share with me so that I can understand more as Mum tells me nothing!

Click to view carold's profile
Hi PearlB

Im so glad you posted that I have exactly the same cancer as you and was told on thursday im to have the same treatment as you too, so its really helpful to me to know what to expect. I know we all react differently but to speak to someone who has already been there is great. I have to have the scan to give me my tattoo blue dots and when having that done they will give me my treatment timetable. Somehow after reading everything on this thread I dont feel quite so scared, cheers all lol xxx

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