Who knew that your hair falling out would hurt? I had been told that my hair would begin to fall out approx. 14 days after my first chemo. Oddly enough, when I woke up in the morning, I didn't have a bunch of hair on my pillow like so many other people describe. When I brushed my hair though, that's when I saw it...all of my beautiful hair stuck to the brush and on the floor. My social worker at the hospital advised that I should cut my hair shorter to get used to that look before it all fell out. My feeling was, what is the point in cutting half of it off if it's just going to fall out anyways?
I lasted exactly 18 days after my first chemo which I guess is longer than most. At that point, when I washed and dried my hair, it was coming out pretty fast and furious so I went to get it chopped off. The place where I got my wig was able to tie my hair into small pony tails and cut those so I could keep the majority of it either to donate or for extensions later on. At first as the hairdresser started cutting, I wondered if I could have waited another few days but it turned out this was the right time as when tying one of the pony tails, she pulled it right off my head!
The social worker explained that for many people, loosing their hair is the worst part. You have to mourn the loss of it before you are able to move on. I cried as each pony tail was being cut but found that after the shock of looking in the mirror, I put on my wig and was myself again. A lot of people say that you will not want to wear your wig at home because it is uncomfortable but I wear it from when I wake up in the morning to when I go to bed at night. Everyone is different and my recommendation is to do whatever you are comfortable with.
I am 30 years old and was diagnosed with breast cancer, specifically invasive ductal carcinoma. Before my diagnosis, I didn't even know what that meant. Now I have been forced into a reality where I not only know what it means but my doctors appointments and daily thoughts are filled with other previously unfamiliar words like neoadjuvant therapy, metastases, HER2 and triple negative.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
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