Today’s post is from one of our younger beneficiaries who has kindly agreed to share her story. Josephine, 26, from London suffered awful reactions to nearly all the treatments she underwent but has since found many complementary approaches to support her recovery.
I was diagnosed at 24 years old in the spring of 2014, May to be exact, following an operation to remove what they thought was something called an “Intraductal Papilloma”.
I initially found the lump on Valentine’s Day, or rather my partner did. It was a very small pea-size lump under my nipple. I made a GP appointment soon after and got referred to the breast unit at The Royal Free Hospital. They did a mammogram, ultrasound and biopsy and told me that I didn't have cancer but they wanted to remove the lump.
They told me I should celebrate! How wrong they were… and how sad it was, because I did celebrate and thought that would be the end of it.
On the surgery day I was then told they needed to “re-check the tissue”. Low and behold, two weeks later I was called in early and told that it was cancer; grade 2, invasive lobular carcinoma, highly oestrogen and progesterone positive.
I was diagnosed at 24 years old in the spring of 2014, May to be exact, following an operation to remove what they thought was something called an “Intraductal Papilloma”.
I initially found the lump on Valentine’s Day, or rather my partner did. It was a very small pea-size lump under my nipple. I made a GP appointment soon after and got referred to the breast unit at The Royal Free Hospital. They did a mammogram, ultrasound and biopsy and told me that I didn't have cancer but they wanted to remove the lump.
They told me I should celebrate! How wrong they were… and how sad it was, because I did celebrate and thought that would be the end of it.
On the surgery day I was then told they needed to “re-check the tissue”. Low and behold, two weeks later I was called in early and told that it was cancer; grade 2, invasive lobular carcinoma, highly oestrogen and progesterone positive.