myth and stigma about sickle cell kano
TRANSCRIPT
The Myth, Stigma & TruthAbout
Sickle CellBy
Murtala Lawal KazaureConvener
Sickle Cell Survivors Forum08030584263, [email protected]
© Sickle Cell Survivors Forum 2015
Presentation Outline• Personal Introduction• Presentation Goal• About SCSForum• The Myth• The Stigma • The Truth• My Story• Q and A
© Sickle Cell Survivors Forum 2015
Personal Introduction
• Name: Murtala Lawal Kazaure• Age: 36 years• Marital Status: Married (Father of 2 Muhammads)• Hobby: Reading, Writing and Struggle• Professions: I.T and Farming• Education:
B.Sc Computer Science (U.D.U Sokoto)M.M e-Learning Tech and Knowledge Mgt (Multimedia University Malaysia)Cisco Certified Network Associate (Cisco Systems USA)C-Tech Certified Instructor (C-Tech Inc USA)
© Sickle Cell Survivors Forum 2015
Presentation Goal
To Clear the General Misconceptions about
Sickle Cell
© Sickle Cell Survivors Forum 2015
About SCSForum• What? SCSForum stands for: Sickle Cell Survivors Forum• Where? The Headquarters of SCSForum is located @ Kazaure• When? SCSForum was initiated in the year 2015• Why? The aims of the Forum are:• To have an avenue where Sickle Cell Patients and their Family and Friends
meet to share experiences and exchange ideas• To help and encourage affected individuals through Advises, Mentoring and
Inspirations• To reduce the harmful misconceptions about the disease• To promote unity and fellowship among Sickle Cell Patients • To educate general public about the significance of testing their Genotype
before marriage © Sickle Cell Survivors Forum 2015
The Myth• I cannot have children with Sickle Cell because I do not
have Sickle Cell and no one in my family does either• We are both carriers, so if we have 4 children only 1 of
them will be Sick• SCD is a Communicable Disease• SCD Patients are drug addicts• SCD Patients do not grow to adulthood• SCD Patients are mentally challenged• THERE IS NO CURE FOR SCD !!!
© Sickle Cell Survivors Forum 2015
Myth is an idea or storythat is believed by many peopleBUT THAT IS NOT TRUE
The StigmaThe general misperceptions of patients with SCD are;• They are victims and cannot do the things that most
people do• They are going to die younger, so no need to struggle
for life• Nobody is going to marry them (both males and
females)
© Sickle Cell Survivors Forum 2015
Stigma is a mark of disgrace associatedwith a particular circumstance,quality or person
The Truth• Sickle Cell Patients are WARRIORS when they decides to be• They can ACHIEVE whatever they want if they develop the
mindset• Sickle Cell is not a COMMUNICABLE Disease• People with Sickle Cell can LIVE UP TO 60 and beyond• Mostly Sickle Cell Patients are very intelligent and have virtuous
mental capabilities• THERE ARE SEVERAL CURES FOR SICKLE CELL(Bone-Marrow Transplant, Stem-Cell Transplant, Genetic Cloning…………)
© Sickle Cell Survivors Forum 2015
My Story 1
Kazaure 1979 Rano 1983
Magwan SPS Kano 1985-1991
Science Collage Lautai Gumel 1994-1997GSS Kazaure 1991-1994
U.D.U Sokoto 1999-2005
Delta State 2007
Info
rmat
ics In
stitu
te 2
006
CCNA 2010
Working with both IIITKzr and HAFEDPOLY 2006-2010
Malaysia 2013-2014 Cyberjaya Malaysia
My Story 2
My Family, My Backbone, My Pillars, My Strength
As a WARRIOR I do unusual things that are not common among SICKLERS
COMING SOON………. Ga ta nan a cikin jini na,
ta nakasta Varaguzai na,
ta kasarta bagauniya na,
ta dusashe kazarniya na,
da ruwan Vargon jiki na
Raxaxi a cikin qashi na,
Xingishi tafiya a guna,
Bani bacci don na kwana,
Da'iman zogi da quna,
Wa ya sanya wuta jiki naaaaa!
Q and A