Kkbbth
7 years agoMember
Discussion & tips
hello fellow peeps,
I am a kick ass 34 yo woman who was diagnosed June 7th with stage 2 BC in my left breast & lyphnodes. I’ve had a double mastectomy June 18th and now I’m awaiting to have IVF then Chemo, hormone and radiation therapy.
Im healing well, had my first infill into my expanders and basically feel like things are moving fasting than me currently.
My biggest concern to date is navigating the system. I self funded my surgery in the private system and now seeing the same surgeon in the public system but I’m yet to meet with or been given the information about my next stage... chemo and hormone treatment. I find that I am very proactive in my journey however it’s hard what to ask, research when you do not yet know what you need to know.
I have sourced a fabulous practitioner that specialised in Lymphoedema & prevention - this was something I found was not mentioned at all during my surgery or hospital after surgery.
What are people’s thoughts about prevention, protective garments and asking for blood tests in the feet rather than the arms now lyphnodes have been removed?
Any tips are welcomed... so glad to have this site & peeps to support and be supported.
Kharj
I am a kick ass 34 yo woman who was diagnosed June 7th with stage 2 BC in my left breast & lyphnodes. I’ve had a double mastectomy June 18th and now I’m awaiting to have IVF then Chemo, hormone and radiation therapy.
Im healing well, had my first infill into my expanders and basically feel like things are moving fasting than me currently.
My biggest concern to date is navigating the system. I self funded my surgery in the private system and now seeing the same surgeon in the public system but I’m yet to meet with or been given the information about my next stage... chemo and hormone treatment. I find that I am very proactive in my journey however it’s hard what to ask, research when you do not yet know what you need to know.
I have sourced a fabulous practitioner that specialised in Lymphoedema & prevention - this was something I found was not mentioned at all during my surgery or hospital after surgery.
What are people’s thoughts about prevention, protective garments and asking for blood tests in the feet rather than the arms now lyphnodes have been removed?
Any tips are welcomed... so glad to have this site & peeps to support and be supported.
Kharj