Stone90
3 years agoMember
Young Mum
Hello everyone, I'm so grateful for this online community. It's been an overwhelming time for me. I was diagnosed on the 23/12/22 and had a really tough two weeks as I was unable to access any support just being to the time of year it was.
I was breastfeeding my 20 month year old at the time, and didn't feel a lump, but just a weird sensation in my breast at random times during the day. I'm so grateful that my GP took it seriously enough to send me for an US. I have Grade 2 ER+ve, PR +ve 11mm x 4mm in my left breast. I'm 32 years old, and my Mum also has metastatic breast cancer (diagnosed at age 69, now she's 72). That wasn't a fun conversation telling her on Christmas Day.
Reading through other people's experiences it seems that going public can be quite slow. I'm also finding that. It took about 5 weeks from me first going to the GP to getting my diagnosis, and I just found out today that my surgery has been pushed back from the 30th Jan to the 3rd of Feb. I understand things happen, but I had already organised childcare for my week post surgery and a friend was coming to stay to give me a hand. I do now get to drop off my son for his first day of kindy the day before surgery, so that's a bonus.
I just want to get the treatment started so I can get past this part of life and back to being me.
Does anyone have any advice over caring for 2 kids under 5 whilst on this journey? I'm so worried about not being able to be the Mum I want to be.
I was breastfeeding my 20 month year old at the time, and didn't feel a lump, but just a weird sensation in my breast at random times during the day. I'm so grateful that my GP took it seriously enough to send me for an US. I have Grade 2 ER+ve, PR +ve 11mm x 4mm in my left breast. I'm 32 years old, and my Mum also has metastatic breast cancer (diagnosed at age 69, now she's 72). That wasn't a fun conversation telling her on Christmas Day.
Reading through other people's experiences it seems that going public can be quite slow. I'm also finding that. It took about 5 weeks from me first going to the GP to getting my diagnosis, and I just found out today that my surgery has been pushed back from the 30th Jan to the 3rd of Feb. I understand things happen, but I had already organised childcare for my week post surgery and a friend was coming to stay to give me a hand. I do now get to drop off my son for his first day of kindy the day before surgery, so that's a bonus.
I just want to get the treatment started so I can get past this part of life and back to being me.
Does anyone have any advice over caring for 2 kids under 5 whilst on this journey? I'm so worried about not being able to be the Mum I want to be.