Anal squamous cell cancer

Is there anyone on here who has had anal squamous cell cancer x

  • Hi Suzmy

    Mumis improving, we are waiting for care package to be put in place then she can come home.

    my joy has been short lived have had vomiting and diarrhoea this afternoon, which I think is the effects of the chemo. All seems to have calmed down now but if it re-occurs will contact acute oncology.

    cant wait to be where you are now.

    Lynne xx

  • Hiya Lynne, Glad to hear your mom will be home soon. Like I said, it's a lovely feeling to think you've got thru the treatment, but my worst time was the first week immediately after treatment finished! I eventually took to my bed and stayed there for about 5 days. Then I started to see improvements. Once my asking started to heal it healed quickly, the tiredness was crippling at times, I've noticed this week (4 weeks after treatment finished) that I'm not as tired and able to do more. My bowels do strange things, I have a day that I seem to spend on the toilet but then I get a few days now that I feel normal. The only pain I feel now is if I'm constantly on the loo. I don't get the runs, it's just a feeling that I need to go, occasionally I have to rush for the loo but not very often. I'm not on any meds now. Sue xx
  • Hi Mandy,

    Can  you remind me?  Was yours caught early?   I think I'm having a hard time because by the time I got a third opinion and treatment started I was already pretty sick and underweight.  I wasn't where I needed to be to tackle the treatment.  Dairy doesn't bother me, but fatty foods make me nauseated and cause tummy aches.  I'm watching the fat content and trying to keep it at 3%.  It's hard to do and it doesn't put weight back on like I need so desperately.  I have a gastro doc appointment next Tuesday to go over what she will be looking for during the colonoscopy.  ugh  I spoke with the surgeon's PA today and she said it takes 2-4 weeks to recover from gallbladder surgery (diarrhea).  That's my biggest concern because I had such a hard time with it the last 2 weeks of treatment.  I've learned how to get it under control, but it apparently comes with the surgery and the body adjusting to it.  I prefer to just go ahead and get it out but the docs think it's better to rule out everything first.  

    It has been much better as far as being able to make it to the potty.  Like Suzy, some days are better than others.  When I do have a lot of gas/wind, it's uncontrollable, super loud and unlike any gas I've experienced prior to this ordeal.  It's like a volcano in my stomach.  Thankfully I do not have that issue every day.  It is still painful to go to the potty.  It must have to do with the location of the ulcerated area.  I do not itch either.  I did during treatment but it wasn't too bad.  A good scratch while in the shower seemed to do the trick.  I think several of us are dealing with acid reflux due to the chemo.  

    None of you ladies experienced hair loss, correct?  I didn't go bald, but I lost most of my hair.  I don't know how to explain it.  I only had a whispy thin layer over the top of everything that had fallen out so I cut it super short.  I think it will look better in a couple of months.  

    Lynn, I'm sorry you are having a rough go of it.   I hope the days fly by for you and that you are feeling much better real soon. 

    You ladies are always in my thoughts.

    Sheri xx

  • Hi Sheri, Its good to hear from you. Although mine was I guess caught before it spread to any other part of the body it was advanced, ulcerated and 6.5cm long. I was although healthy and had no idea or side effects other than experienced what I thought was piles? Not that I had ever had them before. When I went to the Dr I was sent off straight away - diagnosed 10th Jan and treatment started 19th Feb. I finished 29th March and have had a follow up with Dr and will have MRI on 11th June. Like before treatment I feel fine. I went back to work pretty much straight away. I just had 4 days after the Easter hols to get over it. I feel lucky as I had no side effects from the chemo...no sickness (didn't take any sickness tablets given), ulcers in mouth or anything else. The only difference for me is wind. I was never a windy person before but not once I have eaten I know I will want to let rip! sorry for the description ;) I lost no hair - other than down below which is still missing - the odd hair or two but nothing else. I have had no reflux either....my worst experience was the breaking down of the skin week 5 and 6. After treatment wasn't worse for me it just gradually got better and as I said before I finished on 29th March and back into work on Monday 9th April buy finishing an hour earlier so that I could go back home for a rest ......I felt a little tired but now I am back as I was before (other than windy!). I wonder if its the position of the tumour that effects people in different way as mine was very large in comparison with some of the other girls on this site. Most were 2 or 3cm and mine was double this....It was ulcerated and I did have 3 lymph nodes possibly effected.... Sorry to hear about Lynn experiencing a rough time but I am sure within a week things will start to improve for her.... I constantly think of you and all the girls on this site. Its been a journey for all of us......including partners and family. Wishing you the best. Take care of yourself...Mandy x
  • Great news Lynne, well done for getting through it all.

    I'm 3 weeks out of treatment and feel really good and well, just tiredness is the only thing stopping me now!

    Rest up and look after yourself xx

    To all the lovely ladies on here, what an amazing bunch we all are! Hope everyone has a lovely bank holiday xx

  • Hiya Girls, So we are all through our treatments now? Doesn't seem that long ago when we were waiting. Funny how the treatments have affected us all differently. Mandy you seem to have had the biggest tumour but got on better with the treatment than the rest of us. I didn't think mine was too bad especially as I'd had surgery first so my tumour had gone, but got all the chemo side effects you could think of. I'm so glad it's over now, I'm not back at work yet but I'm being told it's super busy there at the moment and I know once I go back I'll be run off my feet. So I'm taking my time, I never usually have time off and I've only got 2 years till I retire so I'm taking my time. We will have to all stay in touch and try to organise a reunion sometime next year. Sue xx
  • Hi Sue and all the other lovely ladies....... Yes we'll have to get together......its been such a pleasure keeping in touch with you all....I feel that I know you all quite intimately now - my little bum buddies :) wishing you all well xx
  • Hi Mandy,  Mercy!  Yours was huge!  You must have been in great condition before starting treatment.  I also wonder if the position of the tumor might make a difference on how fast it heals.  But doesn't all poop end up there and would irritate when passing through?  Such lovely things to think about.  Do you take probiotics?  My doc recommended them.

    I wish I could find a cooking class for people with tummy issues.  Several people on a Facebook website swear by the alkaline diet.  But the American Institute for Cancer Research doesn't agree with it.  Medicare will not pay for a dietician, nutritionist or for psycological counseling.  I have discovered that if I eat what I want (ice cream, cream puffs, whipping cream, Mexican food, anything decadent) I have to go to the bathroom pretty immediately after eating and go often.  So I try to avoid high sugar and high fat foods.  The docs suggested a low fiber diet to avoid the painful exit.  

    Suzy, you earned the time you are taking and you deserve it.  Give your body a chance to heal and have some fun before you go back to work. 

    Lisa, I'm so glad you are doing well!  The worse is over.  

    Gilliebean, whatcha been up to?  

    I think of all of you ladies often.  Looking forward to hearing about Sandy's trip. 

    Hugs to all, Sheri

     

  • Hi Sheri, yes your right it was a big one! I was shocked when told. I don’t know the position but I was extremely healthy and still feel the same. I have always had a good diet. I eat lots of fruit and veg and don’t even have a tablet in the house..I’ve never needed any. I guess I have been lucky and now it’s quite different. Isn’t this type of cancer prone to fair skin, freckly skin or moles...? It would be interesting to know from the other girls if they are in this category. I hope you manage to sort the diet that suits you .....do the other girls watch what they eat? Do they require a low fibre diet? I know the dr at the hospital suggested this when I was on tablets from them for fear of diareah but I never needed to change it. I don’t feel anything has changed for me other than more windy as I said before. I have my MRI on the 11th then the dr appointment the following week. I just hope due to its size it’s shrunk enough! Fingers crossed. Wishing you all well and Sheri I am sure it will settle down soon and you will begin to feel a lot better. Thinking of you always...Mandy x
  • Hi everyone 

    glad you all seem to be doing well and have survived treatment!  I m starting to pick up now at last but the gastric is still a problem ( like Sherri) I have to be so careful what I eat no meat ,dairy or pastries of any kind which really limits the diet but a small price to pay! I can still feel the lump but hope that it's free from the dreaded nasties! Scans on the 15 th June and then a 6 week wait for the results which I m not happy about really but that's the waiting time this end for things to be processed because of the NHS cuts :( just keeping everything crossed that it will be a good result. Think of you all every day what a journey this has been!  I m so glad that there is so much positivity amongst us I suffered terrible nerve pains in my legs and hips for 2 months but they seem to have gone now I m so relieved! Still have to walk slowly as my legs feel like lumps of lead but  I'm sure in time that ll get better too.

    sending lots of love to you all and hope you all get good results from your scans etc. 

    Gilliebean xxx