"I can also
make and sell
my jewellery
and not feel
completely dependent
on something or someone.
I am
my own woman."
In the second part of our conversation with Marie, she bravely opens up about her personal struggle with Sickle-cell, and retrospectively explains how this has motivated her to become more independent in her career ambitions.
And so the conversation continues …
Starting Again & (Re-)Building Her Independence
When I arrived in London, I was able to manage my Sickle-cell. But I made a mistake. If you get any infections or any colds, you have to go and see your GP. If you forget about that, you're making your life a lot worse. But I said “oh, it's Sickle-cell, I know how to manage it”.
I am also a representative for a renal focus group. When I started to go on dialysis, I didn't understand anything and its impact to my health. And I believe this lack of education about kidney donors and dialysis is very common within the black community. So as a representative, I try to promote awareness about organ donation to black people because successful matches or compatibility really does depend on genetics and race. So the more black people that are aware, then more black people can donate their organs, and therefore more lives of black people can be helped.
Educating Thy Self
We will continue this conversation in our Part 3 post, where Marie provides her own perspective on living as a black person in Europe and her experiences with social integration in France. Leave your comments below to continue to support Yaaya’s vision of providing platforms to voice powerful stories of incredible women like Marie-Maimoona Jeannot.
Image Source | These images do not belong to Yaaya. Images courtesy of Marie-Maimoona Jeannot (Light Of Marie Jewels)