Advice: Hi, just wondered if anyone has... - My Ovacome

My Ovacome

18,349 members20,425 posts

Advice

positive profile image
9 Replies

Hi, just wondered if anyone has experience of Liposomal Doxorubicin for PPC. I am to start it in 3 weeks for 3rd line treatment. Only had 5-6months respite between others. My scan is unclear, hazy and I have just had nearly 4 litres drained from my abdomen. I am beginning to not feel as positive as I once was and wondered if The Carboplatin & Carbopltin & Taxol haven't worked very well is this going to be any better.

Thanks

Sue x

Written by
positive profile image
positive
To view profiles and participate in discussions please or .
Read more about...
9 Replies
jennybutler profile image
jennybutler

I only had a short remission and on my 3rd line now, can not tell how long what ever chemo. We are given some get longer on ones that not so long on others wishing you the best results and stay positive,

Love Jenny xx

positive profile image
positive in reply tojennybutler

Thanks a lot for your reply, I do tell myself exactly what you have said but just sometimes wish so much that someone soon will find the right drug to help us all.

All the best for a longer remission

Love Sue

sharonforce profile image
sharonforce

Hi Sue

I had it four years ago along with carboplatin for the spread of my ovarian cancer. I found the side effects a lot more tolerable than carbo/taxol and it did give me 10 months remission.

Good luck with your treatment.

Best wishes

Sharon

positive profile image
positive in reply tosharonforce

Thankyou Sharon for your kind reply. I will keep my fingers crossed it gives me a bit longer.

Love Sue

Jorja profile image
Jorja

I have just had 6 rounds of this drug, last one was 2nd July, had carbo and Taxol in 2008 and 2010, they told me this drug stays in the body longer, did not lose my hair this time, did find first 2 rounds made me feel a bit anxious and not in control of my emotions which I never had with carbo and Taxol, but when had the third round I was waiting for these feelings to kick in and they never did, I felt ok, tired but ok, they told me to watch out for my hands and feet, because this drug can cause what they call hand and foot syndrome, where some people experience reddening, pain, peeling and blisters, I did get a couple of small blisters on my fingers and one on one of my toes, had to be careful with hot water because skin slightly more sensitive to heat, tell your Dr if this happens, but other than the tiredness I sailed through the last 3 rounds, I made sure I put plenty of moisturiser on my hands so they wouldn't dry out, also made sure I took some bowel softener before chemo because after first one was very constipated, took it night before chemo and on morning of chemo, made a big difference second time around I'm not saying this is what you may experience but just giving you heads up, I still had the carbo with it though. Had my post check up Wednesday and they said scans showed cancer had shrunk and was stable, they are just giving me 3 monthly check ups again unless I get any symptoms they need to know about, I hope all goes well for you, stay positive and do what you want or can do, good luck. Jorja. P.S this drug is a red colour, they gave it to me after the carbo on the day not before which seemed to make a difference to the anxiety feeling of the first 2 months where they had given it to me before the carbo.

positive profile image
positive in reply toJorja

Thanks Jorja, will keep all your points in mind. I regularly take movicol as the bowel has always been troublesome and it seems to do the trick. Also take flaxseed which is good.

All the best.

Sue

Snoopy01 profile image
Snoopy01

Hi I was on it for a short while earlier this year - one thing to really watch is reduction in white blood count level with doxy . On the plus side i did not lose my hair again which was great. Good luck and all best wishes for your treatment

Big hugs

Fiona

positive profile image
positive in reply toSnoopy01

Thanks for your advice & would be nice not to loose my hair again so will keep fingers crossed.

All the best.

Love Sue

Suzy profile image
Suzy

I shall be watching replies to your post as I am more or less in the same boat as you (5th line of treatment in my case over 4 years 8 months ) Sue

Not what you're looking for?

You may also like...

New to site, advice please.

Hi......I recently discovered this site and wanted to say how pleased I have. It is so useful to...
Jo-Jo1-UK profile image

Any advice please?

Hello, I am new to this friendly site although I have been diagnosed with stage3 oc since Feb 2007....
Georgesgirl profile image

Newly diagnosed seeks advice

Hi. I joined this site on Friday after just receiving my diagnosis of serous adeno carcinoma. It...
Susie_50-s profile image

Advice

Hi there, I'm new to this site so hi everyone. I was diagnosed with low grade serous ovarian cancer...
RosieDott profile image

Advice re cough/2mo post surgery/strain

Ladies, have had a rotten cold/sore throat/cough for past 2 weeks. I'm 2 months post surgery, but...

Moderation team

See all

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.