me

Hi Toni,  There are two things that have really helped me. The first is the cold cap, which is available at the Mater hospital at Crows Nest in Sydney, I believe it is available in Adelaide as well. I have still retained all of my hair even after two sessions of chemo, I have two sessions  to go.  There is a minor amount of discomfort for a minute or two, when they change the cap,(which is changed every half hour) but that is better than losing your hair. I am in NIB and it is all covered by them.

 The second is a product called Ribraxx. I have been taking it for three months now, I purchased it through a Naturepath. I have hardly noticed the symptoms of  chemo, within a day or two, I feel completely normal again. No nausea, no mouth problems, no nothing.My appetite does'nt change, in fact I was out at a restaurant eating Indian two days after my first chemo.  My friends and family are amazed, when they see me. I feel  Ribraxx has saved me.

I hope this information will help you or anyone else reading this.

Good luck and best wishes.

Judy.

Hi Toni,  There are two things that have really helped me. The first is the cold cap, which is available at the Mater hospital at Crows Nest in Sydney, I believe it is available in Adelaide as well. I have still retained all of my hair even after two sessions of chemo, I have two sessions  to go.  There is a minor amount of discomfort for a minute or two, when they change the cap,(which is changed every half hour) but that is better than losing your hair. I am in NIB and it is all covered by them.

 The second is a product called Ribraxx. I have been taking it for three months now, I purchased it through a Naturepath. I have hardly noticed the symptoms of  chemo, within a day or two, I feel completely normal again. No nausea, no mouth problems, no nothing.My appetite does'nt change, in fact I was out at a restaurant eating Indian two days after my first chemo.  My friends and family are amazed, when they see me. I feel  Ribraxx has saved me.

I hope this information will help you or anyone else reading this.

Good luck and best wishes.

Judy.

Toni.. let me be the first to welcome you to this site... like everyone you will talk to I understand where you are.. been there done that.. and yes, it is very overwhelming when you are just starting out, there is so much to take in, but..believe me it does get better.

I had a lumpectomy and sentional node biopsy in April. I finished Chemo (3 lots of FEC over 12 weeks and 9 weeks of Taxol) last Thursday and start Radium at the end of September.... like you, I'll then go onto the hormone blocking therapy when this is all over.  I lost my hair.. bought a wig which I don't use ( toooo hot!!) and am now a 'Fuzz Nutt'... my hair is growing back... at the moment it is about 1 cm long and baby soft (and grey!!)

It is scary... I still cry and ask 'why me?' But most of the time I'm okay.... as you will be... Chemo is doable, rought but you can and will get through it. There are some scary stories on this site but they are real and unfortunately people are going through them... but you have to remember everyone diagnosis is different.... the positive and helpful stories are inspiring... it's a great place to ask questions and get support... sometimes just blogging helps...

take care and feel free to ask any questions...

Trina

hello toni, l'm still coming to terms with my diagnoses and that was back in march of this year. They say it gets easier with time, but its a hard thing to accept and move on from. For me its a constant reminder as l have needed the breast removed, and the operations are endless- thats how it feels. as for the scars, thats another story.

although l have not needed chemo or radio, l'm afraid, really afraid it will come back in the other breast. l guess we have to learn to live with that constant fear that crops up especially when we are alone. l have to learn to live with the diagnoses and fear as well-even though it's really tough at times.