Paying for Avastin: Hi there. The Parp isn’t... - My Ovacome

My Ovacome

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Paying for Avastin

dramaredgerbil profile image
10 Replies

Hi there. The Parp isn’t working and it’s sadly chemo time again so soon. I will be given weekly taxol and I plan to pay privately for Avastin. Can anyone advice me on this?

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dramaredgerbil profile image
dramaredgerbil
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10 Replies
vipervictoria profile image
vipervictoria

Hi, I don't know the treatment you've had already, but there was a study in this week's Oncology Practice Update that showed good results from a combination of Gemcitabine & Pazopanib, especially in women who are platinum resistant. Here's a link: practiceupdate.com/c/98700/....

Hope it's worth a read. Good luck, VV

Neona profile image
Neona in reply to vipervictoria

Thanks this is interesting!

dramaredgerbil profile image
dramaredgerbil in reply to vipervictoria

Thank you. I’ll have a look. Are you in the UK?

Queta profile image
Queta

Hi I am living in Orlando and i am qualified for the laboratory paid for the treatmnet i don't know if you can contac to them and you can qualified for this help too

Good luck and many blessings

Eiram63 profile image
Eiram63

Hi. I received weekly paclitaxol along with three weekly carboplatin and avastin for a total of 18 weeks. There was a break in the middle for surgery. Now I just receive Avastin every three weeks for 13 cycles. I am now nearing the end and have just one more to go in two weeks time.

Blood results show that when I started 15 month ago my CA125 was in 1000's. Now it is as low as 12 12 and has remained so for months

I feel so apprehensive finishing Avastin. I felt so comforted to know that every three weeks anything horrid rearing it's ugly head would be zapped. I think I am going to be paranoid now with every twinge ache etc.

I am not sure if Avastin has given me side effects as I can't decipher myself whether what I experience is still side effects from chemo, from the cancer ir from surgery.

I have been back at work full time since October. I am not at full speed still, however energy is improving. Brain improving too. Lol. I do suffer badly with painful neuropathy in my feet which has worsened. This i don't know if it is Avastin causing or as I said still late chemo effects.

Have your doctors recommended avastin for you? Is it expensive? I would certainly have more if I had the option. My last chemo was last July and so far bloods and scans are all good. For me, Avastin seems to have worked and mentally I will do miss it

Hope my experience so helps you

Eiram63 profile image
Eiram63

Hi again. Is there not a trial available that could help.? I am on icon8b, however it was my first illness. I was stage 3 high grade serous. I just read your profile and you seem truly amazing in all that you have done. So sad there was a recurrence. I know that is what we always face with this disease. I didn't realise that there is an option to pay for avastin. Have you had it before?

dramaredgerbil profile image
dramaredgerbil in reply to Eiram63

When first diagnosed, I was on the Icon 8b trial. Had a remission of two years. I’m going for private Avastin to add to Taxol which is the NHS standardised treatment. I read about a trial that improved prognosis. It will cost me in the region of £2500/3000 a month. Using my pension pot and savings. What good is money if im not hear to spend it. I’ve found a company called Healthcare at Home and will go with that but still waiting for more information. I think it’s the taxol that gives you neuropathy. Where do you live?

Eiram63 profile image
Eiram63 in reply to dramaredgerbil

Hi. I live in Coventry. I finished taxol 8 month ago now and feet are certainly no better. Getting worse if anything. Will NHS not provide Avastin again then?

dramaredgerbil profile image
dramaredgerbil in reply to Eiram63

No. Unless you can get on a trial. Has Taxol shrunk your tumors?

ZenaJ profile image
ZenaJ

Sorry I can't help as I was never offered Avastin but I believe it's something you do after chemo. Best wishes, Zena x

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