Here we go again....: Well after a reoccurrence I... - My Ovacome

My Ovacome

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Here we go again....

8 Replies

Well after a reoccurrence I’m starting my new chemo treatment today, more nervous than I thought I’d be having been through it before and I think it’s because I don’t know how I will react to this specific chemo, caelyx. My good friend Sue is coming with me, my hubby takes us and leaves us to natter away the time Sue also provides the snacks LOL

Got all my moisturisers & mouth washes ready and just hope my side effects aren’t to severe.

Anyway ladies I wish you all the best on your own journeys xxx

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8 Replies
Irisisme profile image
Irisisme

Hello Scotty,

It's good that you'll have your friend with you, we try to be brave but do really need people to lean on, hug us, and to natter with to distract us!

Hope it goes well.

Iris XX

Katmal-UK profile image
Katmal-UK

Good luck Scotty, hope it goes well. Hope the snacks are nice!! xx Kathy xx

Lily-Anne profile image
Lily-Anne

Good luck with your infusion. Caelyx seems to be the drug of the moment.

A friend with snacks, sounds like my kind of friend lol

LA xx

Seasun36-uk profile image
Seasun36-uk

All the best for your new chemo regime....and here’s to no (or very few!) side effects! Lxx

ShropshireJo profile image
ShropshireJo

Sending you my very best wishes and hopes that you cope with the treatment well. Glad you’ve got a good friend to help pass the time. My lovely sister sat with me through the endless hours of carbo/taxol. It made a huge difference. Jo 🌸🌻🌼🌺🌹

Neona profile image
Neona

Wishing you good luck.

HI Scotty. Just would like to wish you all best with Caelyx, I've had quite a bit of experience with this treatment with good results yes the side effect can be hard but all manageable.

I managed to keep my part time job through out the treatment'

Take care Lorraine xx💙💙

Ge0rg1na profile image
Ge0rg1na

Yes, we carry on, that's what we do, isn't it?

Great to have a friend to support you but there are also some benefits from going alone. You're more likely to engage with other fellow sufferers and I've developed a great group at the London hospital I attend but I can't tell you how happy I am that my sister is arriving from Australia tomorrow. She will be staying with me for 5 weeks so a bit of respite for me. She will also relieve me from supporting mother, 88 and needy.

But this is about you, so my advice is to take everything one step at a time. Don't worry about later on, it's an unknown at every stage, so use your energy to deal with today. Enjoy your friend's presence today and get into a treatment routine. Pace yourself!

We're here for you - every day/night. Gina xx

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