Hello ladies! Oh Dear! Its the 20th May already! Wasnt expecting it this earlyxx
Well done Racerxx
Hello racer, great news! Well done for those blood results! Re the blood on your pillow, I sometimes have very small nose bleeds, and my Onc has said it is the Cape. Worth you getting it checked out, though. Keep an eye out in the meantime.
Hello marli - sorry, I thought that was your daily dose, not your twice daily dose! That is actually quite a high dose then! I'm currently on 1800mg twice daily making it a daily dose of 3600mg. I started on 4000mg per day, though, and then it was reduced after about 7 cycles.
Thanks for the info, Kirky.
My dose is now 2150mg morning and evening ,4300mg a day. I am only 5ft and weigh 11st 7 so think that is normal dose according to Google. So hope that is about it. So far so good. Marli x
Hi Barton, if dose is morning and night that's the max dose for someone of medium build. I was on 2500 (5000 per day) but am 5'10 and 12 stone. Reduced back down to 1500 @ 2 after s/e on the max.
Hello marli, sorry to read about your stents - that sounds nasty! I have not had to self- cathetherise, but I do have to be very careful as my kidneys are a bit "funny", in that I have a generally high (higher than the average) level of bilirubin, and a high Creatinine level - so I have to drink a lot each day. I did have to have an Ultrsound a few weeks ago to make sure my urine was not going back up the tubes to my kidneys (it wasn't, luckily). That was because of an extremely high Creatinine level for that cycles' chemo - I wasn't allowed to have it that cycle. It seems to have been a one-off luckily as it has come down since to what is more or less normal for me.
What I'm (finally!) getting round to is that is there an alternative to the stents for you? Has your Onc told you to try drinking more?
Re your Onc increasing your dose of Cape, I think that is still quite a low dose compared to most people. However, if you are a tiny person with a small frame and very slim, that could easily be right. I was told the dose was based on your weight to height ratio.
Sorry I can't be of much help. I would definitely say it's worth asking your Onc if there are other alternatives, though.
Hello ladies - hope everyone is continuing to stay well. Had to smile at racers comment that Oncs. don't tell us things early only when they cause a problem.
I'm finding that at he moment regarding kidney stents. Was told I need them to keep kidneys healthy to deal with chemo. Wasn't told that they could be uncomfortable and would need replacing every 3-6 months, which involves an op with general anaesthetic. Now been told that I will need to self catheterise to ensure that the bladder is emptied completely. I'm very uneasy about this. Anyone else had this?.
Started 2nd round of cape after seeing onc yesterday and she increased the dose to 2150mg ( from 1650Mg) so I am hoping that it does not cause me too much of a problem with se's. She checked the lumps and bumps that I was worried about and they are OK ( one in tummy is a hernia from laparoscopy for biopsy!!) Kidneys are slightly larger and presumption is urine retention hence problem with stents.
Blimey if its not one thing it is another! Continue to stay well ladies. Marli xxx
Hello George, yes - we have rain too - not for 3 days though!
Glad you are feeling better! Glad you are getting an extended rest from Cape and that Tamoxifen is working for you.
Enjoy your feel good stuff.
Hello George, I hope you had a wonderful time in Valencia?
Well done for doing the Race for Life - wow! I am really impressed, and such a lot of money raised, too!
Fingers crossed for continuing on Tamoxifen! Good luck for the Onc visit - let us know how you get on.
Well done Angela for your 7th cycle of Cape. Re sugary drinks, it also something I am very aware of. I can't bear the taste of plain water these days after having to take all these tablets. I used to love water, but now I only find it bearable if it is ice cold. I do always take my tablets with plain (ice cold) water. However, as I am supposed to drink a lot, I have a three-quarter full glass of water, which I top up with fizzy lemonade - only a very small amount, but it is enough to add some flavour to the water without drinking full glasses of it. I don't actually like fully fizzy drinks - I would rather drink them half flat, so adding them to water helps in that regard too.
Thats very encouraging to hear, racer! Well done! Sorry about the borderline diabetes though - I know it's just one more thing for you to have to think about. Glad your platelets are so good and have stabilised. Also good news that you can continue with Cape and that it is helping you. Glad also to read you haven't suffered vomiting for a week. Good news almost all the way round! It always encourages the rest of us to get good news.
Hugs, and fingers crossed as requested! Barton.x
That is good news racer. Have been following hour posts since I joi ed this thread and it is reassuring to know it is working. Have a lovely weekend. Marli. Xx
Thanks for that info, Carolyn - I didn't know that!
Moijan, I think they do that at our hospital, too, but not sure if it is the actual morning of my appointment - that would be much more useful.
Yes, Sandra, That would have p d me off too...I obviously hadnt realised. Actually, my primary got missed, so now attend elsewhere and i currently get copies of drs letters, but im very happy with my onc..the oncs all have group discussions with the radiols /other specialists on the morning of my appointment....I guess thats what might happen everywhere.. They are closely watching an area for me, which will be reveiwed with a bunch of scans in a few weeks.
Have noted some muddly bits in gp letters written by junior doctors in the oncs absence tho
very best wishes,
Hello Sandra, so sorry to read of your progression - worrying, isn't it? However, I'm glad to hear at least someone seems to be on top of things for you. Well done on completing your 6th cycle. I hope the Vinorelbine/Cape combo works for you.
I hope you have a lovely week away for your birthday. It's my 60th this year, too - it seems quite a lot of us on the boards are hitting that milestone this year!
Hugs and best wishes. Barton.x
Well done, marli! Tiredness is an issue I'm afraid - I think it's the stress that the chemo puts on your body - it is designed to kill cells, although hopefully the cancer cells go first! However, it does kill ordinary cells as well, so the body has to work hard to replace the necessary ones!
Sorry you are also experiencing nausea. Luckily, I haven't had that as an se, but I can see how debilitating it could be.
Hugs, and enjoy your week off! Barton.x
Hi Sandra and a very Happy 60th Birthday today 🎂🎈🎉🎁😊🍾 Shoukd we now call you Sandra60? 😉
Have you anything nice planned? If not it sounds like your short break is just what you need to take your mind off everything. It dies me and my OH wonders when we get away as when you are in dufferent surroundings you do manage to forget about the dreaded SBC! Enjoy.
As to your onc, he is a bit of a liability isn't he? Thank goodness the radiologist did interpret the results - as they should do. Chemo does help with aches and pains with your bones as I've found over the years so it could be worth giving Cape a few more cycles on its own before your onc adds another chemo? Just a thought. And if you really aren't happy with him you can get a second opinion to check you're on the right course of treatment but still get care/treatment at your local hospital, you don't necessarily have to change unless you go onto something involving a trial which tend to be done at the larger cancer centres.
Anyway, get on and enjoy yourself on your special day.
I would, but this is not the first time. I had a bone scan prior to starting cape in January, my Onc told me it was clear and the considerable pain I was in was nothing to do with cancer. I saw the Macmillan Nurse 6 weeks later who looked through all my reports and told me that the radiologist strongly felt that there was metastasis in my hip and ribs. When I next saw my Onc I asked him about it and he was very vague and wouldn't comment.
I hope everyone else is getting on well with cape and managing to enjoy life, I am looking forward to a week away next week and a change of scenery.
Hugs to you all
i think cons Radiologists are the most expert at reading the scan....wonder if hed been away, or maybe behind in his checking of scans, my own onc said last week that the rads cons had picked up on Some progression when mine was reviewed on the morning before my appointment....
So, give your onc the benefit of the doubtxx
hoping all. Is going as well as, Moijanxx
Just finished my 6th cycle of cape and the only side effect I have had had been the complete lack of energy to do anything, I didn't even bother to take my anti sickness tablets during the last cycle as the nurse told me I didn't have to. I had my CT scan after the 4th cycle and results after the 5th, my Onc was happy with the results and told me to carry on with cape as the lymph nodes in my chest have shrunk, as there were no problems, my next appointment was with the oncoligy Nurse last Monday. Everything was fine on Monday and I picked up my next lot of cape. When I got home there was a message on the answer phone from the Onc's secretary saying that he needed to see me before my next appointment. So it was back to the hospital today, 25 miles away, and a wait of 1.5 hrs to be told that the radiologist has reviewed my scan and decided that there is progression of the cancer in my ribs and pelvis, my Onc had previously written to my GP saying that he didn't know why I was in pain with my ribs and the pain in my hip had been put down to arthritis, the pain in both areas has decreased since I have been on chemo. They are going to add vinorelbine to the cape along with bone juice but I am not starting it for 10 days as we are going away for a few days to celebrate my 60th birthday tomorrow, at least I have got an extra week off cape while we are away! I didn't have much confidence in my Oncologist before, I have even less now, but at least someone else reviewed my scan and picked up on the deterioration.
Good morning ladies, a lovely sunny morning here today. Hope everyone is doing well today.
Finished my first 2 weeks of tablets this morning. Things seem to have been OK without any major se's.
The major problem has been fatigue with a little nausea. For the first 11 days I was so tired I could not be bothered to answer message and texts or even to talk to my husband at times. The most activity I did was 20 minutes shopping and then have 2 hours sleep. Looking back over the last 2 weeks I realise that I was feeling somewhat depressed , which really is not me.
However, reading back on this thread I did find it reassuring that this seems to be normal.
Well let's see what my week off brings. Thank you for your support. Marli x
Hi racer and good to hear from you. I'm glad you got away for a couple of days but sounds like it was a bit too much for you overall, I hope you have managed to rest since and feel a bit better.
Helen - great news and good for you planning a few holidays. We have always done that once settled into a new treatment regime so we're hoping to plan something soon after a few months uncertainty about which treatment to move on to.
Hello racer, in answer to a couple of your questions: Yes, my hair has definitely thinned. I think this is mostly due to the Cape, but it was a little thinner before, possibly due to the hormone therapies. Also, no, no sweet cravings, but I tend to crave savoury stuff! I am actually, off (to some extent anyway) chocolate! I know - weird!
That is wonderful news, Helen! Thank you so much for sharing and cheering us all up!
Wow, you have got a busy time ahead, but the best kind of busy - HOLIDAYS!!! I hope you enjoy every second of them - you deserve it.
Hugs and best wishes - long may Stable Mable reign.
Hi cape Crusaders... dropping in to share some happly news..just done cycle 8 on cape and scan results show no progression :-))) Very pleased.
I have felt very fatigued the last 2 cycles so my onc and I have agreed to move to 2 weeks on 2 weeks off. Not had a dose reduction.
Planning many trips over the net few months.. Spain for May half term with the kids, weekend in Cambridge at a humanist conference, Stonehenge Summer Solstice festival, Camp Bestival with the kids and most excitingly 2 weeks with hubby touring Europe in his camper van in July. I love this chemo, apart from my poorly feet!
Hugs to all xxxxxxxx
Hello racer, thanks for retirement info - yes, really looking forward to it, but still feel a bit like I'm on holiday at the moment!
I am sorry you had so many problems on your short break away. I hope you managed to have a good time some of the time. Bourton on the Water is lovely, although it is many years since I have been.
Good luck on Thursday with your next Onc appointment. Please let us know how you get on. Glad you feel good about the Cape.
lovely to hear from you, but so sorry about the surgeon...must have been traumatic to discover this
recently.....we put our trust in people and then get let down...
hopefully you werent diddled, but do check and see if you are eligible for compensation....
As the other ladies have said, he seems to be doing all the right things but I do know that some people seem to suffer more than others. I was prescribed pyridoxine when my feet and hands became a bit sore, its Vit B6 and supposedly helps. I can't say for sure that it did but I didn't have any real problems with either and only took the tablets when it was bad. You/your hubby should be able to get them from your GP or onc and its a high dose tablet taken about 3 times a day if I remember correctly. Good luck.
To all Cape crusaders - how flippin' cold has it been this Bank Holiday? Brrrrrr. Very chilly today so not doing too much but did go out for the day yesterday to Kew Gardens - beautiful azaleas, rhododendrons and blubells - very uplifting.
Hope you have all been able to enjoy yourselves one way or the other.
Thanks, George. Just more crafting as I need to finish that project. Looking forward to it. Hope you have a good one, too.
What an apt quote, George!
Caffy, hello and welcome again. So sorry about hubbys feet - I know exactly how painful that is! However, he seems to be doing everything right, so not sure what to suggest. I know the Vaseline worked wonders when my feet were bad, but you do have to put your feet up as much as possible a. Because walking whilst squelching and slipping in Vaseline is just horrible (and dangerous!), and, b. Because putting stress on the feet makes things worse. I believe it is because the chemo leaks out of all the tiny capilliaries when pressure is put on them, also when put in hot water. Actually, he could try bathing his feet in chilled water then patting them dry and then creaming them gently. Hope things improve for him soon. Wishing you both all the best.
Marli, love that idea! Just what he deserves! Why are all these dreadful things always perpetrated against women?
Hello again lovely ladies. I 'chatted' to you in here last year when my husband started taking Cape for his Bowel cancer mets. I'm a BC survivor, hence being in this forum! I hope you don't mind me gatecrashing again! My poor hubby is really suffering with his feet, he says it feels like walking on hot coals. He's just had an extra week off but should start again today and is not keen. He uses Aveeno cream and Vaseline, and a heel balm. Any other tips on what he can do? I try and be patient but he is pretty fed up and therefore grumpy about it!!! Wishing you all a lovely bank holiday, hope the weathers better than here in Cornwall! Xxxx