Hey,

 I hope you are having a lovely blessed day. Well, I'm Mimie, Volunteer Online Fundraising Manager at the Sickle Cell UK Society.

I live in London, UK. I love meeting new people and friends from all over the world.

She needs to help by supporting the FIGHT AGAINST SICKLE CELL DISEASE/ FALCIFORMS ANEMIA to give back to both my African and British communities.

This cause has always burned in my heart, she has lost 4 family members (SS sickle cell) and herself, a healthy carrier sickle cell (AS), which is why she is standing up and raising awareness of sickle cell disease/sickle cell anaemia, to the millennium generation specifically.

Her mission as a VOLUNTEER is to RAISE AWARENESS in order to encourage the younger generation to do the genetic screening test (electrophoresis) before marriage to stop the birth of babies born with sickle cell disease in the 21st century.

To all, who aspire to marriage, no one is safe and don't be ignorant, do your *red hemoglobin electrophoresis test to protect your offspring!!!
Better safe than sorry! Saying.

Sickle cell disease or sickle cell anaemia is the first incurable genetic and hereditary disease in the world; but which can be STOPPED, so that no more children with sickle cell anaemia are born, by a simple intelligent and responsible decision of the two spouses/partners to have their screening test done before contracting the marriage.

Let's FIGHT against sickle cell disease, the first genetic and hereditary disease.

Together let's STOP sickle cell babies from being born.

Together we will defeat sickle cell disease and find a CURE.

This is our way to make this world a better place to live in.

Together we can, together we’re STRONGER.

 

Join and be part of our volunteering team. Visit our web site to fill out the volunteer application form 

https://www.fautinengalulamukinayicommunity.co.uk/

Salut!

Luttons contre la drépanocytose, première maladie génétique et héréditaire.
Ensemble, empêchons les bébés drépanocytaires de naître.

Ensemble, nous vaincrons la drépanocytose et trouverons un remède. C'est notre façon de faire de ce monde un endroit où il fait bon vivre.

Ensemble, nous pouvons, ensemble, nous sommes PLUS FORTS. 

Rejoignez et faites partie de notre équipe de bénévoles. Visitez notre site web pour remplir le formulaire de demande de bénévolat.

https://www.fautinengalulamukinayicommunity.co.uk/