Sorry to hear that you are having a hard time on Tamofoxen - have you spoken to your doctors about it? I am on Letrozole which is a pain, but manageable at the moment - hoping that some of the side effects will calm down after a few months - been taking it since the end of August. I went to a Moving Forward session at the hospital with a couple of nurses and they said to get in touch if we didn't cope with some of the side effects - they have different things they can give you, or might ask for you to be changed to another drug.
Sorry to hear about your sister Aussie - it's tough watching someone else - I watched my brother go through cancer treatment, and lots of drugs - it's difficult - it's good that you spent time with her - that's what counts.
I'm back at work doing my normal hours (22) which is good - being back in my normal routine, with people I know and get on well with - they've been very supportive. It is still difficult though when people ask if I'm feeling better - I am of course, but don't know if I will ever feel completely better - it changes your life and how you feel about things - plus of course the aches and pains that I know have as part of the letrozole, my nails are still not good, and my hair is growing back, but I'm still wearing hats and scarves. Maybe in 6 months things will be more normal - but who knows - still get constantly reminded which is very frustrating when a lot of the time I feel fine.
Anyway - that's my rant over. Hope everyone else is doing ok. I had a cocktail a couple of weeks ago - fabulous!, and also had some wine and proscecco since then - and planning more when I head of to Lanzarote for a week soon.
Good to hear how you are going ,and some good news stories, After I finished chemo in July had my surgery or first part and now i am half way through radiotherapy which is okay so far , I am a bit pink and my tissue expander is getting quite firm but I half to have that out anyway at some stage.
I went to the UK just now too to see my sister who also has BC however sadly hers was stage 4 at diagnosis and is now in her brain just 18months later so it is so awful. It is being treated by whole brain radiotherapy , we had a cruise booked for us all to go but she was advised not too which was a real shame however I went and it was a nice break
I will pop over to the rads thread too
take care everyone
Good to hear you have finished radiotherapy too. I think you are right to make sure you have given yourself time to get over the ordeal before returning to work. I don't feel too bad because I only ended up having two lots of chemo and that was back in April so my body has had more time to recover in between the various stages of treatment which has helped. My hair has started to come back and is a silver/grey pixie crop at the moment- not what I am used to but actually doesn't look too bad! It has come back very soft. My eyebrows are still patchy so I am getting used to using wunderbrow on those. I didn't lose my eyelashes thankfully.
I like the sound of a break in the New Year. I hope you enjoy Venice.
Take care and all the best to you and all the other March starters out there.
Hi Helen, Ruth & any other March ladies out there,
Lovely to hear your news, so nice to hear of positive things like weddings and holidays....Helen - Barbados how lovely! Ruth I'm so glad to hear you were well enough to enjoy your daughters wedding.
I finished radiotherapy last week. Due to my sensitive skin issues I had 30 RT treatments over 6 weeks. RT went well until this week when the skin has broken done a bit under the breast. So recovering from the treatment at the moment and feeling a bit tired but very happy that treatment is over. I'll probably get back to work after Christmas as I feel I need the rest. Treatment is over but you're left a bit knackered. I've still got achy legs, especially at night. I'm having Herceptin (3 weekly til next May) for a full year so my treatment is sort of ongoing but side effects seem to be minimal.
Hows everyone's hair situation? Hellesbelles I recall you cold capped so kept most of your hair? Mine is 'action man' style but even coverage and quite thick. Growing slowly - can't see a first hair cut/trim being needed for a while. And I have eyelashes growing, what a joy to see them. Never thought I would say that happiness is......eyelashes! Brows are patchy but definitely back too. It's such a relief to see yourself emerging again.
Just booking a trip to Venice for the new year.
Love & best wishes to all.
Hi. Sounds like you have had something good to look forward to and enjoy after all the treatments. You must have been so ready for a good holiday so hope Barbados did the trick! Congratulations on your 50th. I am sure you hadn't imagined being in the midst of a cancer diagnosis for that but glad you could celebrate. My daughter's wedding was a lovely day and I felt well enough to enjoy it to the full. It was really nice to have a happy occasion to celebrate between my op and the radiotherapy starting. I finished my treatment on Tuesday so am going to rest up and take it easy for a bit before I return to work in a few weeks. My cancer was triple negative so I can't take any hormone tablets - I just have to trust that the treatment has done the trick! All the best for a healthy and happy future. Ruth x
Hi Helllesbelles. I moved to the September radiotherapy thread but this popped up as a notification- how are you doing? Ruth
Hello all! Suuny here in London, hope it is with you too. I am so relieved chemo is over. Must admit, a week after my last chemo I was very tearful and low. I think the reality of what I'd been through in the last five months hit me.
Leyla, that sounds awful about your thumb nail. I hope it is not too painful and recovers soon. Must be really awkward to manage with. I'd agree withRuthElisabeth's advice about your lumpectomy. Mine was back in January, before chemo, and I had no trouble at all with either of the surgery sites (boob and armpit) although my boob did swell up afterwards - I must have gone up a couple of cup sizes on one side and could hardly put my arm against my side! But the fluid soon dispersed, and I do the lymphodema exercises to get my lymph system working well.
I wear a M&S camisole with a hidden shelf to bed every night still, just stops anything pulling on my boob and scars.
RuthElizabeth I'm so pleased to hear about your daugther's wedding, how special for you and your family.
Really good to hear that lots of us are progressing through radiotherapy too. Mine starts on Monday (your last day I think, Moonstruck) I have 23 days, so will finish on 6th September. Honestly not worried about RT at all. The team at the hospital were super when I went for my scan and tattoos (my first ever!). A good friend who went through breast cancer three years ago has given me some organic aloe vera gel, which she has advised I keep in the fridge so it is super cooling on hot skin.
Anyone else taking tamoxifen? I started on Monday, so far so good, just hot flushes, which I was getting with chemo anyway.
Next step is waiting for my head hair, eyebrows and eyelashes to grow back. My eyes water like crazy too. I'm happy if all the other body hairs don't bother to come back! Apparently facial hair is a side effect of tamoxifen - now that is ironic after the trauma of losing hair through chemo 😉
And best news of all, this morning I had a cup of tea for the first time in months! My last docetaxol was 11th July and it seems my tatse buds are nearly recovered. Simple pleasures mean so much.
Hope you're all doing well. I'm halfway through radiotherapy now, I was just starting to feel more like mysellf again and now I have a sore pink chest. Oh well! I think generally, now it's over, I was lucky with the taxol. I kept my hair and nails, although my eyelashes look wierd still my brows are back. Neuropathy more or less gone. I've started working out once a week with a trainer and am going on holiday after my final radiotherapy session, trying to keep looking forwards to good things rather than brooding.
Anyone on any of the radiotherapy boards on here?
Hello all. It is good to catch up with you all on here. It feels like we are old friends even though we haven't met! It's good to hear that most of you are well on the way to the end of treatment - what an adventure this year has been! We all need to pamper ourselves when all this is over - a relaxing holiday and meals that we can actually taste when our taste buds return. Give ourselves time to rest and recuperate because we have been through a lot! I was pleased that I felt well enough to enjoy my daughter's wedding at the weekend - together with painted on wunderbrow eyebrows and wig! My surgeon and oncologist were both very pleased with the results of my treatment and I am in the process of being referred on for radiotherapy- possibly starting at the end of August for 3 weeks.
Leyla - hope your op goes well on the 10th. I had a lumpectomy and it wasn't too sore afterwards. The bit that was worse was the sentinel node biopsy as the wound under my arm meant I couldn't move my arm much. I would suggest taking in pjs and tops with buttons down the front - nothing that needs to go over your head! Don't try stretching it too much or lifting anything heavy for a while. Also my surgeon gave me a frontfastening sports bra to wear post surgery which really helped and I even slept in it. It kept the wound still so that it didn't pull on the scar.
Well, all the best to everyone- wishing everyone good results and good outcomes and a healthy future xx
I finished my chemo 3 July such a relief then had surgery on 21 July masectomy with tissue expander in as have radio next, Although Chemo is not fun it did its job as my tumour was 95% gone so surgeon was very happy and I am getting used to the tissue expander which does feel like a brick on my chest but gradually settling down and then I can think about next bit
I have a little bit of hair too but no eyebrows or lashes so eyes water non stop but on the whole I feel so much better than a month ago mostly I think its the relief of the surgery and chemo bit over with
Now I am pleased I did the chemo first as it gave me time to look at surgery options
anyway I hope everyone is okay and feeling okay its such a surreal time and many days I cant still beleive it but I am going out more often for walks and feeling more normal so I take great comfort from that
All the best to all with whatever stage you are up to
Hello ladies, great to hear your updates. Well done to those who have completed chemo, and all not long now for the others. I had my final treatment (FEC) on 30th June so have 4 more days until end of cycle and end of chemo! I had the usual tiredness and nausea but have been feeling strong for about a week now. I went to ladies day and Newmarket races on Thursday it was lovely yo leave the house for somewhere other than the hospital! I was still on antibiotics and antifungal so didn't drink but had the best time with 25 other mums from my village. Today I went to Cambridge to watch my sister and 6 of my lovely friends complete Race for Life. They did it as Team Leyla. I was so touched that they wanted to do it. They were all so awesome and they raised nearly £1800!!!!!!!
I saw my surgeon last week and have my lumpectomy booked for 10th August. My final MRI I had just before my last chemo showed the lump had shrunk some more and was less dense. So pleased! Any pre or post surgery advice would be most appreciated.
Take care ladies, we are all awesome 😃👊🏻💪🏻 Lxx
Well done on finishing your last chemo. I had my last Dox on Monday so unfortunately are going through the horrible data at the moment, I keep telling myself I haven't got to endure this again!! I think this last one has been harder on the bones, just like cartwheel said the pain could be new cells. It's my shins and ankles that aches. My taste buds seem to be worse this time around. I have been sat here today thinking that we are normally on holiday now every year!! Well just think ladies thus time next year we will be having our fantastic holidays and getting on with our life's again. I just can wait to get back to normal, start the diet!!?i am 50 on Wednesday, so I feel I have double celebration due to getting through to the end of chemo and 50!!!I have asked my family fir a treadmill so I can get rid of my chemo belly and thighs!! I would love to be normal again now. Not long!! Keep up the good work ladies and stay strong xxx
Well done on finishing your last chemo. I had my last Dox on Monday so unfortunately are going through the horrible data at the moment, I keep telling myself I haven't got to endure this again!! I think this last one has been harder on the bones, just like cartwheel said the pain could be new cells. It's my shins and ankles that aches. My taste buds seem to be worse this time around. I have been sat here today thinking that we are normally on holiday now every year!! Well just think ladies thus time next year we will be having our fantastic holidays and getting on with our life's again. I just can wait to get back to normal, start the diet!!?i am 50 on Wednesday, I have asked my family fir a treadmill so I can get rid of my chemo belly and thighs!! I would love to be normal again now. Not long!! Keep up the good work ladies and stay strong xxx
I've just had my last docetaxol. I found it much more tolerable than FEC.
Water retention hasn't been an issue for me. The main side effects are pain, so I alternate ibuprofen and paracetomel to manage the pain, my mouth feeling slimy, and fatigue.
I have a couple of baths a day, epsom salts are great for easing the leg pain and tense shoulders which I also get.
Thanks Mojan, I'll look up the cream you mention. I've just got a bit of new drug anxiety but looking forward to getting another treatment out of the way.
Hi ladies and well done to all of you as you near the chemo finish line. 💪🏼 🏅
Im from the May starters thread and have reached half way after 4 X FEC! I start my Docetaxol next Thursday (all being well, since I was hospitalised for 4 days last week wth neutropenia - until then I'd been doing really well). Do you have any tips? I have all of the constipation & sore mouth treatments on the planet and I'm told Loratadine is good for bone pain. I try and eat mushrooms and cantaloupe melon daily to reduce side effects and boost immune system. I notice you've had sore eyes so I've bought some goldeneye drops in anticipation. Does anyone have difficulty with fluid retention on Docetaxol? Xx
I know the taste buds thing is one of the worst side effects and i did not expect that ,
even drinking water is hard going , for me I cant eat chocolate at th moment it tastes so slimy so its mostly toast and jacket potatoes lots of carbs but as I am not doing a great deal they are not the best thing to eat but I couldnt face a salad at the moment !
Meash67mosh, the pain in my pelvis is at the front and down the front of my upper thighs (apparently it's the bone marrow in the pelvic bone making new blood cells). I feel like I want to stretch out my hips when the pain comes.
Moonstruck, good luck with radiotherapy today. Agree with you about tatse buds - I haven't enjoyed a cup of tea in months!
Good to read all of your updates. My first radiotherapy session is this afternoon - they put some markers on me with a red dye that I can't see. Hoping I won't get too tired - I'm fed up being tired - but however it goes it can't be as bad as chemotherapy!
Eliza sorry to hear that your chemo was delayed. Hope it went OK yesterday. Aussiegonewrong good luck with mastectomy and that it's not too long till you get a holiday.
I agree with folk who say they are feeling fat and ugly - I've put on weight too - lack of exercise and comfort eating. My eyes are still dry in the morning and then streaming during the day - very annoying! However I do feel more normal with a clearer head most of the time - looking forward to being able to taste food properly again - the simple things in life.
We've all been through so much and I agree that radiotherapy should be straightforward after chemo - getting near to the finish line and having a normal boring life again!
Take care everyone - looking forward as always to a relaxing holiday somewhere!
Nice to hear you are all coming to an end.
I hope your chemo has gone as well as expected for your last, just think yes 5 days of feeling sh@t but you don't have to go back for more!!! Well done you are a survivor, up to cancer ladies👍👍🍾🍾🎈🎉🎈🎊.
I have very dry eyes in a morning where they have ran during the night too, my legs start to ache about now so have just had a nice bath, feeling very hot!! Think I am also having hot flushes starting. I have radiotherapy measure up next Monday, think it will start about 1st August for 4 weeks, everyone keeps telling me very tiring due to going every day but a walk in the park compared with chemo. Has any put much weight on, I seem to have put a stone on!!! Cartwheels is your pain in the pelvis at the front or back?
Moonstruck how how are you finding radiotherapy is it tiring, do you have tattoos on?
keep going ladies and share all our near end stories as they are very helpful as usual. Love to all you brave, caurasious ladies xx
So near to the finish line now!
Aussiegonewrong, hope you feel better soon. My eyes water too, I often have to wear sunglasses even on non-sunny days because of any grit in the air. At least the sunnies also cover up my very sparse eye lashes. Good luck with your surgery next week.
Meash67mosh, hope your last docetaxol went ok. Your pattern of rough days is exactly the same as mine. Have my last round tomorrow so Thursday evening to Tuesday will be a write off. But at least it's the last time!
Eliza, you're right it's my last chemo tomorrow - we can think of each other! My eyelashes are sparse but I still have a few. But I don't bother with mascara as my eyes water so much I end up looking like Alice Cooper. My once thick eyebrows are now sparse, but I have enough to be able to draw them in (I love Wunderbrow). Despite cold cap, my hair has continued to fall out on docetaxol. I now have a bald patch on the top of my head so I look like Friar Tuck! I feel really self conscious in my wig, so I have mastered the art of tying headscarves. I really don't want to burn my lily white scalp in the blazing sunshine.
Moonstruck, hope radiotherapy is going well.
I think I'm having hot flushes, but it's hard to tell with this heatwave we've been having. The filgastrim injections make me quite feverish for a couple of days. I've woken up at night with sweat dripping off my face and chin. Yuck! I'm so glad this will be the last lot of the injections and the accompanying pelvis pain.
I see my doctor about radiotherpay on Wednesday, but that should start in 4 weeks from now. My oncologist wants to start me on tamoxifen at the same time. A whole new set of side effects to navigate! But at least no more chemo - hallelujah.
Well done all, we're amazing. Thanks for continuing to share your stories.
I too can relate I handled the Fec alot easier than the the Docetaxal , I had my last one a week ago such a good feeling walking out of the chemo unit but now a week later feel awful , mouth slimey face puce and watery eyes and no energy , I know it will end but I wish it would hurry up , I have in the past managed to go to work but I look so awful and its all too hard to try and fix as watery eyes mean no make up stays on so I am taking time off and I agree its hard not to feel sorry for yourself sometimes even though hopefully the worse bit is over. When I go out for a walk I have to stop to catch my breath too
I have my surgery 21st masectomy with expander and then radio and then will do the remaining bit of the reconstruction after that
Good luck to all with last chemo and radio , I too would love a holiday i havent had any alcohol since diagnosis couldnt face it and probably at the moment would taste awful but a nice glass of champers in the sunshine would be magic
I can relate to all your symptoms and SE. I have been very, very tired this last week too, I'm so knackered and my legs ache so bloody much. I have my last chemo tomorrow of doc can't bloody wait to get it out of the way. I no I will feel fine Tuesday but crap on Wednesday, Thursday, Friday, sat, sun. But I no in my heart now that thus is the last time I am going to feel crap. Eliza I feel for you as we all no what you are going through. I feel ugly, fat and just don't want to go far, I can't anyway as I'm knackered out of breath and legs ache. We are all fantastic strong ladies, we can overcome anything now we have gone through chemo!!!!
i will try to post on here this week Eliza if I feel up to it, please stay in touch let me know how you are feeling. Keep telling yourselves ladies nearly there!! I also have radio appointment next week 17th for measurements.
Love to you all, we are nearly there 👍👍👍👍👍😀😀😀xx
Eliza here. Great to hear your updates, I've not posted for a bit as I've found Docetaxol a bit more challenging after a relatively easy ride on EC.
Congratulations to those who have had their final treatment or are heading that way. The shared experiences on here have been a great comfort to me personally. I've had a 5 day delay due to a persistent dry cough, Consultant wanted to check lungs and heart which were fine thank goodness. So my final chemotherapy is this Tuesday 11/07. I am relieved to be having it but also not looking forward to it, I'm sure you all know what I mean. Radiotherapy is booked, the first set up scan is August 1st then treatment starts a week later. I'm having a lower dose over a longer period (6 weeks- yikes) but this is because I have had so many skin reactions during chemotherapy they think it'll be kinder. Had a lovely bout of acne during No 5 and major stomach rash they thought was shingles....
I have tried so hard to remain positive and 'up' during this process - I have to admit I'm now struggling - I feel knackered, ugly and rather anti social. Listen to me! I need to give myself a good kick up the backside....! Ironically the great weather does not help, sunlight feels wrong. My eyes water, my face goes puce.... longing for a holiday where I'm back to normal and can stick my flip flopped feet in a sparky pool......
Just out of interest, how are you all getting on with the eyelash/brow situation? I started off as with mega werewolf brows so mine are just hanging on in there, weirdly the left is so much thinner than the right. Lovely. Same with eyelashes left almost zero, right a fair few. Got a bit of head hair growth, can't see much but feels a bit action man velvety.
HellesBelles congrats on getting through radiotherapy. You've done so well. Wish I could've met up in Bath but definitely in a few months if you're up for it. RuthElizabeth hope you're recovered from both ops and your radiotherapy can start soon. Meash and Cartwheels are you joining me in your final chemo this week?
Hope all you ladies are ok and getting through it or if you've finished hope you're enjoying increased wellbeing as you recover from treatment.
Love to all,
Hi Hellesbelles - congratulations on reaching the end of your treatment- it must feel so good! Glad your hair has come back and you can start dying it. My hair has started to come back now - very soft at the moment. I had my second op this week and will hopefully be starting radiotherapy in a few weeks time if my biopsy comes back clear. I have heard from others too that it is tiring - I will have an hour journey to get there but I am hoping my husband will be able to take me so I don't have to do all the driving. I finally got to a Look Good Feel Better session this week which was a great pick-me-up just before my op. Got lots of tips ready for the wedding in a few weeks. I couldn't believe the products in the goody bag too - so much better than the usual brands I use! Best wishes and hugs to all of you lovely ladies who have been sharing this journey xx
Hope that you are all doing well. I'm now on day 8 after my last chemo and getting frustrated that I still feel tired and dizzy so every time I do something I have to sit down after 30 minutes. I went out yesterday for a walk around the block as I was getting stir crazy and was exhausted when I got home - just being impatient I suppose to put the chemo all behind me.
Good to know that some folk have started radiotherapy - mine starts in 2 weeks. I was told that the main side effect was tiredness and that it is cumulative as Hellesbelles has said - I am hoping that it won't be too bad as I would really like to get away for a few days at some point - need a change of scene and be somewhere where I feel like I am on holiday - even if it is only an hour away from home. I was also told that the targeted area will get red and sore, possible with a rash - has anyone had that yet? The Doctor I spoke to also said that it can take a few weeks to recover after the end of the treatment - but everyone is different as they always say.
My hair has started to grow back too - bits are white and others are darker, but I suspect it will mainly be grey - no point expecting miracles! - how long does hair have to be before you can have it dyed?
Meash67mosh - I have been having aches in my arm where I had surgery too - and numbness too like you.
I feel that the worst is over, but radiotherapy is still a bit of an unknown - but if we can cope with chemo then we can cope with anything.
Hope you have sunshine where you are and that it's warmer than it is here is Scotland - only 13 degrees at the moment xx
I haven't been on for a while either, not had a good first week of chemo but feel better now. It is so nice to hear that all of us are coming to an end of our chemo and we have come through it. It has been hard in some way or another for all of us but I think by being positive and exchanging notes, thoughts, remedies we have stayed positive and focused. I have my last chemo on 10th July, I have been told I will have 4 weeks radiotherapy, I am just wondering when it will start now. I have had one good thing happen! My hair has started to grow, it is 3 colours by the looks of it!!!! I am normally dark brown so it might be grey, brown, white or blonde. But it's mine and that's all that matters. Does anyone else have aches where there surgery was at all from time to time. I had lymph nodes clearance to and that area is still numb.
good luck ladies with remaining chemo or radiotherapy we are nearly there. 👍👍xxx
Just wanted to thank you all for your support and advice on here. I'm now at nearly 3 weeks PFC and am amazed at how much better i feel. I did 12 weeks taxol. I had shooting pains and mild neuropathy all the way through but they have almost gone. I did walk every day. My hair did not fall out (I cold capped and used Daniel Field products) and my nails are also fine (i used Hydrogel gloves and slippers). I lost some eyebrows and eyelashes. Taxol is of course less severe than a lot of other treatments.
My main worry has been pain and swelling on my side and arm where the surgery on my armpit took place. I found a lymphoedema physiotherapist who massages my side and shoulder and the pain seems to have almost gone. I still don't know if it is or isn't LE but I am very pleased that the pain is lessening.
I hope this will encourage you if you're near the end of treatment. It's amazing how a cloud lifts once you've finished chemo. I still get tired quite easily but feel so much better than I did during it.
WE CAN DO THIS!
It has been quiet online , some other threads very active I noticed however we are getting there, I too have final chemo on Monday cant wait
I am not too bad on the Docetaxal mostly taste buds gone and fatigue but last couple of days my eyes very watery so that is annoying , saw my surgeon last week and I think i am going to have masectomy with expander initally as I have to do radiotherapy and then I may do a diep flap in a few months not sure yet if too have both done but as you can only use your stomach once have to think about that a bit more as big operation so will see the plastic surgeon too so before I decide, Sometimes its so overwhelming can only think about whats happening this week , my hair is also coming back so I will use the cold cap one last time but last week my eyelasehes and brows more or less went , I have been practising drawing them on but not great at that so hope they grow back quickly
Hope everyone doing okay its such a relief to think no more chemo !
It's much quieter here, sounds like many of are coming to the end of our chemo - hooray! Really lovely to hear about some of your plans, it's so good to have events to look forward to. Once I get through chemo I hope to plan a short break to the seaside. I've felt a strong need to stay near my hopsital through chemo.
I had 5th round on Tuedsay (FEC-T), and my last will be 11th July - that day can not come soon enough. I have been so lucky on docetaxol, found the side effects much easier than FEC. The fatigue is cumulative, and my taste buds have desserted me for weeks now, but overall I feel like I've been so lucky. My main ambitions now are for my hair to grow back and to be able to enjoy tea again.
Still waiting to hear when my radiotherapy starts, but by end July I think.
Good luck to all with the next stage in treatment, be it surgery, radiotherapy, hormone therapy or all of them! It's been great to have this forum, even if on many days I've felt more of a **bleep** than participant. Great to know us ladies were all out there getting through this togther.
We're not alone and we're amazing.
That's pain about them having to do more surgery - but hopefully under local anaesthetic it will be quick and straightforward - basis error though. Good news that the cells so far have come back non cancerous.
Good that you have the wedding to look forward to and get excited about - that'll keep you distracted.
Hi Moonstruck - Good to hear from you and great news that you have got to the end of your chemo! Hope the side effects wear off quickly for you. It is quite a while since I had my last chemo and my hair has started to grow back - it is just a short fuzz at the moment. I am just recovering from my surgery and went for my check up on Tuesday and he was happy with now it was all healing up. Problem is that they somehow missed the little coil marker that was put in the lump and an ultrasound shows it is still there. This means I will have to go back for more surgery to remove it! They will put in a wire to mark where it is under local anaesthetic and then go back in to retrieve it! The biopsy they have done doesn't show any signs of cancerous cells remaining but until they check the coil marker I don't feel that I am quite cancer free. I am hoping they will do the radiotherapy after my daughter's wedding so that will be end of August. Each step is a step nearer the end. Best wishes everyone - keep going 😀
I hope that you are all doing okay - it has been very quiet online recently. I was quite down the last time I posted - a low point for me, but I'm okay now - I feel able to look forward now - although it is still frustrating at times - and I am sure you are all the same.
I had my last chemo yesterday and it went quickly for a change - and I was all prepared for the usual delays..
Feels good to not do that again - although still got to get through the side effects though so not done yet.
I start my radiotherapy in 3 weeks which seems quick but the oncologist says that it's fine - so 19 sessions over 4 weeks. Has anyone started that yet - they say it can made you tired and it is cumulative - but everyone is different as ever.
Has anyone's hair started growing back? Mine's is like a white fluff, and my eyebrows have started to come back too - although very light - but it's a start. Went to LGFB last week which was very good -the makeup folk were all lovely and very helpful and got lots of freebies - although I don't wear much makeup it was good to get tips on technique.
Hope you are all enjoying the sunshine (covered up of course) - it's a bit cooler now in Scotland, but supposed to be 18 degrees today - that's hot enough for me.
Take care - Moonxtruck xx