Positives of Treatment (chemo , radiation and hormone therapy )

I will pass on cold caps will embrace the bald and beautiful look with hoop earings .

@chipo Cold caps are supposed to shut down the blood flow to your scalp while you are having your chemo infusion. The technology for the high end caps is very expensive and few regional centres can afford it. There are mid range products that you can rent (or some hospitals can only afford those options) The equipment is often funded through donations or available in hospitals that have surplus funding. It is not life saving and is not federally funded.

As kez can tell you, they certainly work for some people. But, and this is the catch, they do not work for others. No one knows why. Some chemo regimens have some good results, others do not. there are no guarantees
.
Cold caps significantly increase the amount of time you spend in the chair and some people report that it is a painful experience. All that is probably worth it if you keep your hair (or in most cases,some of it)

When the caps fail many people have real mental crash. They are invested in an idea that means they can avoid that most telling sign of being in chemo treatment, baldness, and keep what most of us highly value, our hair. Yet another disappointment which I could personally do without.

Hey, given what you are already managing, you will cope with bald. It's a weird right of passage, but it does pass. Marg xx

@Chipo, the positive thing I held on to was knowing I had thrown everything at this disease to prevent recurrence and metastasis. Yes it's hard doing chemo but I know you can do it cos I did. I found the halfway point I was pretty rough and depressed but I held onto the words my onc gave me at that point -" you will get through this, you will look back on this as just a chapter in your life". I trusted her 100% and clung onto those words although at the time I didn't think there was life without cancer. 
Well, here I am getting close to one year anniversary - lumpectomy and nodes done , tick chemo done tick, mastectomies tick, going to the gym feeling stronger back to work soon. Tick tick tick!!! You can do this!!!! We've got you!!! Xxxx

I'm going to give them a go. Apparently, you know by the second treatment if they're going to work or not.

It's a device that chills the scalp and may prevent hair loss. I haven't used it but there is a whole thread on this site. Worth checking if your day oncology offers this option.

&sister l am going to see the chemo doctor on the 8th . What are cold caps ? 

When do you start chemo @Chipo?  Have you been given the option of cold caps?

Hi @Chipo,


Considering all the yuk things your brain conjures up at the mention of chemo, some of us get through quite ok (much to our surprise I think).

I had 6mths chemo.  AC was a little rugged but a hell of a lot better than I thought it would be.  Occasional nausea throughout.  Heaps of energy on day 2 and 3 from the steroids.  Kept my hair with cold cap, worked, think I only took 4 days off work the whole time, did all my usual stuff and managed to renovate my dining room along the way. I found having little projects going gave me time to focus on something else other than treatment.  Worst part was the bland taste of everything and hot flushes. Luckily wine still tasted the same LOL

Taxol was a lot easier, had minimal issues with that one.   Drove there and back mysef on this one. (Not on the AC, though) Just sensitive to sunlight and a wierd skin rash, but my skin is weird anyway.  Worst part, again hot flushes.

Had 30 rounds of radiation.  Skin held up until about number 24 I think but recovered really quickly as soon as I finished. No fatigue.  The worst part was having to drive there everyday.  

I took lots of photos along the way of everything we did while I was having treatment, then made a video when I was close to finishing to reflect on how much good stuff happened in amongst it.  

For me , the hormone therapy has been the worst, we have not agreed at all.    I did take a few weeks off it and have been back on for 4 weeks.  The side effects have settled somewhat this time around.  Just needed that break to let every rebalance I think. I'll just see how it goes. 

Just remember that the list of side effects they give you is a list of everything that can happen,  doesn't mean it will.

Keep in touch.
XOXOXO

Chipo just adding to what @Afraser
has said above. 
keep asking questions and you can always ask in here 
Postives of Chemo .... no shaving/ or waxing of hair, quicker in shower as no hair wash/conditioning etc  IT doesn't last forever there is normally a time frame of  chemo then rads then hormone therapy. 

It does save us from Breast cancer in the majority of cases. 

I cant give you any idea on hormone therapy as I didnt need it. 

hugs 
Soldiercrab

Hi Chipo
good that you have taken the hair in hand ( so to speak!). Being prepared helps a bit. I haven't had radiation so can't talk about that.
I had no nausea or fatigue (or chemo brain) during chemo and worked throughout. I assumed I would be really sick and I wasn't at all. Yes, I did get a couple of other side effects, but one is probably a mixture of things not just treatment, and the other is comparatively rare. Hormone therapy can have side effects, depending on how you tolerate it but they can also vary a lot. In general terms I would say that chemo is still the best therapy we have to get rid of cancer cells, it's for a fixed period and if you can keep that in mind, and keep looking forward, it's a little bit easier even if you have unpleasant side effects. A lot of people say they find radiation easier than chemo. With hormone therapy, ask for information about the side effects of whichever therapy is recommended, and the benefits. If you have side effects, from anything, don't suffer in silence!! Take it all bit by bit and don't worry too much about what's months ahead, things may change. If you can, and it's not easy, keep as connected as possible to the good things in the world, and the things you look forward to. It's all too easy to let cancer and treatment take over your life. This isn't your life, it's just a part of it, and with any luck, it's a part you will finish and walk away from. Best wishes.