Please share your experiences of EC and docetaxel. Which was easier, worse for side effects?
I’m on 2nd of 3 EC cycles, then onto docetaxel. For some reason I’m scared of docetaxel.
Thank you
Just replying to bump it up.
I found docetaxel easier side effect wise and my hair started growing back, which was a nice surprise. The only thing I would say is don’t take any laxido on your first round. If you think you’re constipated, just wait and eat more fibre/drink more water and see if it gets better before reaching for the laxatives.
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Hi @bluesatsuma I had exactly what you’re going to have. On Monday I will be having my 3rd Docetaxel.
Personally I have found the Docetaxel physically easier then the EC. With EC I had quite a lot of tummy problems, dizziness, lightheadedness and slight nausea. I found all bit the lightheadedness improved as the treatments went on. With the Docetaxel- no nausea or lightheadedness, very little tummy problems- hurrah. The main side effects have been aching joints for a few days as if you’ve had a gym session, not that I ever go 
- I took Paracetamol or ibuprofen. - horrible tasting, furry tongue and loss of taste - savoury food tasted metallic, cardboardy or off!! I needed to eat things with a stronger taste, eg chutney in a sandwich etc. I found sweet things taste near normal - hurrah! I wondered if I had oral thrush and was going to go to the pharmacist when i got up on the morning of the 10th day and it was all totally back to normal - mouth normal, taste back, so it’s unpleasant but short lived!
The other thing I have had is peripheral neuropathy in my feet. Tingling and cramp like pains in the toes mostly. I’m at greater risk as I’m diabetic so I found this quite frightening. I had bouts of a couple of hours in the evening. I discussed it worth the Oncologist and they were happy for me to have the full dosage for the second treatment. It has lasted a bit longer this time but as worth the first time it went by about the 10th day.
I have felt much tireder and each treatment i don’t quite get back to ‘normal’. I don’t think that is the Docetaxel though, I think it’s the cumulative effect of 5 chemotherapies.
So overall i have found the Docetaxel ‘easier’ then the EC. It’s not a walk in the park, and not how I’d chose to spend my time, but there we go.
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Thank you @kartoffel. That is reassuring. Hope I find it similar. I will follow your advice about the constipation. Hope you are well now x
Thank you @pat. Lots of helpful advice there. I’m reassured that you found it easier than EC. The neuropathy worries me but not everyone gets it…maybe I’ll be lucky? Hope that your last chemo goes smoothly and that you start to feel better soon. X
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Thank you for putting your experiences on here. I have just had my final EC and move onto docetaxel on 14 October, and like bluesatsuma was anxious to know about how it went.
All 5he best xx
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It doesn’t seem to be everyone who gets the neuropathy. I used compression socks and gloves whilst receiving the infusion. I took the gloves off when I left the hospital and kept the socks on overnight and didn’t get any neuropathy. Who knows what would have happened if I hadn’t used either but I figured there was very little downside in giving it a go.
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Thank you. I have got compression stockings from surgeries…do you think they’d help?
If they’re like the ones I have, they’ll be too light. You’re aiming to find ones with a compression rating of 20-30mmHg. Compression Therapy Versus Cryotherapy for Chemo Neuropathy | Natural Medicine Journal.
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Also, if anyone is interested in trying compression and doesn’t have the funds: Preloved Reloved has a few donated items that are available free of charge: https://www.instagram.com/prelovedrel0ved?igsh=MWdtaGtiOGpqb3pxag==
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I was on TC so Docetaxel & Cyclophosamide (the C in EC)
Docetaxel gave me mouth sores/oral thrush so I chewed ice during infusion & had meds ready after cycle 1 to mitigate
I used Suzi Pads ref neuropathy but compressions socks / gloves are meant to help too
Never was constipated and had to take Loperamide to stop my poonami (sorry if tmi)
I did have an allergic reaction to it cycle 2 and had have it slowed down to 2 hrs vs 1 with more pre meds for cycle 3 & 4 & a severe rash but that was due to it being done via a cannula but the nurses know what to do
Taste was destroyed lol & I had to have strong foods for first 10 days but again it was fine
All the best ! X
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Oh & I took an antihistamine for bone aches
Start a few a days before chemotherapy & throughout the filgristim injections x
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Thank you @idcand49. Some super tips there too. With EC I’ve had pegfilgrastim so i hope they will give me that for docetaxel too as its only one needle per cycle then. But I’ll definitely bear in mind the advice about antihistamines, ice and compression that I’ve learned here. Thank you…hope you are well on the road to recovery now xxx
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Thank you & glad you have the 1 injection vs 5-7 one (most trusts don’t offer it) that felt like the worst part sometimes
All the best x
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