in celebration of the World Sickle Day,Sickle Cell Advocacy & Management Initiative
Please Join Us for an
Awareness Walk
Walk for Change: Be Sickle Smart
Take off Point: National Stadium End Point: NIMR Hall, Edmund Close, Yaba
Take off time: 8.00am
FOR YOUR BRANDED TSHIRTS and/or CAPS TEXT 0809 800 7264 WITH YOUR NAME NOS & SIZE. Cost: T Shirts 3000, Cap 200 ( this is limited in qty)
and a
Symposium
In Celebration of the World Sickle cell Awareness Day
Under the distinguished chairmanship of Dr Jide Idris, the Lagos State Honourable Commissioner of Health
Theme: 100 YEARS OF SICKLE CELL DISORDER – STILL SEEKING A SOLUTION”
Date Saturday 19th June, 2010.
Venue : NIMR Hall, Nigerian institute of medical research, Edmund Street, behind Presbyterian Church, Yaba, Lagos.
Time: 12noon.
Free Genotype Testing Available
Refreshment follows
Join us in creating more awareness on Sickle Cell Disorder. Its a walk for change. Come in your Jeans and Tshirt.
Tuesday, June 15, 2010
Tuesday, May 25, 2010
Monday, May 24, 2010
JEANS FOR GENES 2... still more pictures
Moyo of IMAGINE CLOTHING with some of the models wearing her designs for the show!
Toni Payne, Designer, with cross section of models with her designs for the show
Toyin, Charles, Zara, Toni, Buki
Emem and Kunle Bello
Eva gets shown some love!
mODE nINE, one of the performers speaking about THESE GENES
Ada, Zaeynab, Ebere and Abiola! All Rocking THESE GENES and these smiles!
All FOR THESE GENES
UnRulies!
Jibola Olubiyi and Bolu
happy Facez!
Cross Section of the designs!
Toni Payne, Designer, with cross section of models with her designs for the show
Toyin, Charles, Zara, Toni, Buki
Emem and Kunle Bello
Eva gets shown some love!
mODE nINE, one of the performers speaking about THESE GENES
Ada, Zaeynab, Ebere and Abiola! All Rocking THESE GENES and these smiles!
All FOR THESE GENES
UnRulies!
Jibola Olubiyi and Bolu
happy Facez!
Cross Section of the designs!
Tuesday, April 20, 2010
Jeans for Genes in more Pictures
Model working the runway in a Polo by OUCH!
(not seen in this picture, but she is wearing sandals by T.T. Dalk Accessories)
Mo Cheddah lenu at Jeans for Genes! Guess she still can't be censored!
Gbemi Olateru-Olagbegi, Tosin Oni, Maynezee, and more faces at the event
Models at the event
zara
POPE na enjoyment!
Media presence at the event
mODEL models Toni Payne
tUNde Aladese models a Happy Facez teeshirt as Baby of Happy Facez explains the teeshirt design!
the Amazing DIPP being interviewed on the Red Carpet
At the exhibition stand!
Tosyn Bucknor and Kunle Bello
(ALL PICTURES ON THIS PAGE COURTESY SEYI CHARLES GEORGE PHOTOGRAPHY)
(not seen in this picture, but she is wearing sandals by T.T. Dalk Accessories)
Mo Cheddah lenu at Jeans for Genes! Guess she still can't be censored!
Gbemi Olateru-Olagbegi, Tosin Oni, Maynezee, and more faces at the event
Models at the event
zara
POPE na enjoyment!
Media presence at the event
mODEL models Toni Payne
tUNde Aladese models a Happy Facez teeshirt as Baby of Happy Facez explains the teeshirt design!
the Amazing DIPP being interviewed on the Red Carpet
At the exhibition stand!
Tosyn Bucknor and Kunle Bello
(ALL PICTURES ON THIS PAGE COURTESY SEYI CHARLES GEORGE PHOTOGRAPHY)
Monday, April 19, 2010
Jeans for Genes in Pictures!
Kunle Snatcha Rooftop (what a mouthful) registers for Jeans for Genes!
Zara the Flyest!
Tosyn Bucknor( These Genes), Kunle Bello and Emem Ema (the M.Cs)
More Accessories, including BUCKSTONE Flip-Flops on display!
Accessories by My Dazzle on display
Toyin Adesola of S.A.M.I.
Kunle (Snatcha of the Rooftop MCs, Ohimai and Mode Nine at the event)
They call him Willy Bang!
EVA
SKALES heads for a grammy at Jeans for Genes 2
FEX at Jeans for Genes 2
(ALL PICTURES ON THIS PAGE COURTESY SEYI CHARLES GEORGE PHOTOGRAPHY)
Zara the Flyest!
Tosyn Bucknor( These Genes), Kunle Bello and Emem Ema (the M.Cs)
More Accessories, including BUCKSTONE Flip-Flops on display!
Accessories by My Dazzle on display
Toyin Adesola of S.A.M.I.
Kunle (Snatcha of the Rooftop MCs, Ohimai and Mode Nine at the event)
They call him Willy Bang!
EVA
SKALES heads for a grammy at Jeans for Genes 2
FEX at Jeans for Genes 2
(ALL PICTURES ON THIS PAGE COURTESY SEYI CHARLES GEORGE PHOTOGRAPHY)
Tuesday, April 6, 2010
Jeans for Genes, the Morning After!
well... maybe several morning afters!
Sorry for the radio silence, but dont worry, we are not planning to pack this blog up and pretend sickle cell never happen
Even though this blog was utilised effectively for the dissemination of information about Jeans for Genes, it was primarily set up to give constant information about sickle cell in general, and one persons journey with sickle cell in particular!
We will have news items for you from time to time, plus interesting fictional and non-fictional posts so please check our blog as often as you can
Heres an idea... Why not subscribe?
yes boss!
So Jeans for Genes 2 finally held after all the pre-show publicity and hype!
It held at Swe and yes, it started right on time (3pm) with the Red Carpet and Market
We had cameras from MTV covering the initial proceedings for our event exhibitor, YAT, i.e, Youth Are Talking. Youth Are Talking focuses on HIV /AIDS awareness
We also had initial backstage craziness, and networking!
That was fun!
The show started proper at about five with a runway mash-up (a mix of tees from various designers, including the YAT and THESE GENES tees!)
And then, music, fashion, music, fashion, music, fashion....
Our thank-yous come soon, and of course, pictures and more details from the show, but just to let you know that we were able to raise some money for SAMI (Sickle-Cell Advocacy and Management Initiative).
We will present them with the money next week, and hopefully, the lady who needs treatment can thank you guys at some point!
Sorry for the radio silence, but dont worry, we are not planning to pack this blog up and pretend sickle cell never happen
Even though this blog was utilised effectively for the dissemination of information about Jeans for Genes, it was primarily set up to give constant information about sickle cell in general, and one persons journey with sickle cell in particular!
We will have news items for you from time to time, plus interesting fictional and non-fictional posts so please check our blog as often as you can
Heres an idea... Why not subscribe?
yes boss!
So Jeans for Genes 2 finally held after all the pre-show publicity and hype!
It held at Swe and yes, it started right on time (3pm) with the Red Carpet and Market
We had cameras from MTV covering the initial proceedings for our event exhibitor, YAT, i.e, Youth Are Talking. Youth Are Talking focuses on HIV /AIDS awareness
We also had initial backstage craziness, and networking!
That was fun!
The show started proper at about five with a runway mash-up (a mix of tees from various designers, including the YAT and THESE GENES tees!)
And then, music, fashion, music, fashion, music, fashion....
Our thank-yous come soon, and of course, pictures and more details from the show, but just to let you know that we were able to raise some money for SAMI (Sickle-Cell Advocacy and Management Initiative).
We will present them with the money next week, and hopefully, the lady who needs treatment can thank you guys at some point!
Tuesday, March 23, 2010
Rocking THESE GENES of mine... a personal story
When i am asked to write about my journey as a person living with sickle-cell, the challenge for me is finding the right balance. I do want to share my experiences and let you know how it felt, and feels, but i also do not want to come across as self-pitying or whining. Then there is the delicate balance between hope and reality. Yes, you can live with these genes, but it is a painful journey no matter how much i try to coat it!
The best thing?
I just write and hope that if one person reads it and feels better, then God's purpose for me continues to be fufilled.
Yes, i have learnt to see my genes as part of my purpose. For any other option would drive me insane. How do you explain to a child that they are living with a disorder that is incurable and was inherited at birth, and came about simply because two people loved each other and brought forth life? How do you, as that child, wrap your head around it?
For me, there were transitions, but the most memorable are the angry, and the happy.Angry was at my mother (oddly, never my father. But i am a fierce daddy's girl), and more importantly, at God. You see, it was impossible for me to understand how God could love me and punish me at the same time. I had wild discussions with Him, i even urged Him to kill me, Once, i was so ill that even the generator got on my nerves and moving a muscle spelt pain. That was my most fun moment because after i spent all my time asking God to take me home, i felt at peace and was no longer angry again! I do not always share this story as it sounds 'spiri koko' (spiritual) but since that day, i knew i had to either wrap my head around this disorder, or let it consume me!
I chose the former.
First, even though i could not remove the cells, i could remove my attitude to them. Instead of hating them, i loved them. Yes oh, even when i would have to be rubbed all over by my mother (sweet mother for real) with transvasin, and sleep with a hot water bottle, all because it was my birthday and i just had to dance. I mean, what is a mother to do; not allow her child a birthday party because she would be in pain later? I loved those cells even when it meant my mother would find some other concoction for me to try next. I mean, i was luckier than most; they never tried to beat the evil out of me abi? I loved my genes oh, even when it meant my father spent more money on hospital bills than school fees when i was growing up, and even though it meant my sister got a little less attention than i did (and i love her for never making me feel bad about that!).
The more i loved the genes, the less they seemed to bother me. And the more i spoke about the genes, the more i found coping strategies. The more i understood the genes, the more i worked around them.
Yes oh, i was the girl in the hospital who would never flinch as they stuck a needle in her arm (I once took fourty eight injections in one famous week), and i was the girl determined to make people laugh because the more they laughed, the less they focused on me and why i was so thin, or why my eyes were yellow!
But as i grew up, i realised that loving but ignoring the cells was not enough. I had to speak up about them. I had to let my friends know that i could hang out with them, but only for this long! And i had to find out from other people living with sickle-cell, what their journey was like! The more i did this, the less it became about me, and the more it became about a nation and a thinking!
Why is sickle-cell practically stigmatised? We should talk about it, and noone should be ashamed to either live with it, or have a family member or friend that lives with it. And why should we deal with it alone when by asking and sharing, we can find more ways of coping with ours? I mean, people have asked me to speak with their friends or family members that live with the disorder but are ashamed or afraid of it, and even though i am not a medical expert, i do enjoy encouraging people!
You can live with sickle-cell. I do. Tope does. Toyin does. Subi does. Jacob does. Tunji does.
Some days, i do not hear from Subomi so i know he has been ill, and i call and we say hello. And vice versa! We are not hiding, and we are not letting our genes stop us from living.
We may not express it the same way, but i think somewhere along the line, we all realised that it really was not how long we lived that mattered, but how well.
The best thing?
I just write and hope that if one person reads it and feels better, then God's purpose for me continues to be fufilled.
Yes, i have learnt to see my genes as part of my purpose. For any other option would drive me insane. How do you explain to a child that they are living with a disorder that is incurable and was inherited at birth, and came about simply because two people loved each other and brought forth life? How do you, as that child, wrap your head around it?
For me, there were transitions, but the most memorable are the angry, and the happy.Angry was at my mother (oddly, never my father. But i am a fierce daddy's girl), and more importantly, at God. You see, it was impossible for me to understand how God could love me and punish me at the same time. I had wild discussions with Him, i even urged Him to kill me, Once, i was so ill that even the generator got on my nerves and moving a muscle spelt pain. That was my most fun moment because after i spent all my time asking God to take me home, i felt at peace and was no longer angry again! I do not always share this story as it sounds 'spiri koko' (spiritual) but since that day, i knew i had to either wrap my head around this disorder, or let it consume me!
I chose the former.
First, even though i could not remove the cells, i could remove my attitude to them. Instead of hating them, i loved them. Yes oh, even when i would have to be rubbed all over by my mother (sweet mother for real) with transvasin, and sleep with a hot water bottle, all because it was my birthday and i just had to dance. I mean, what is a mother to do; not allow her child a birthday party because she would be in pain later? I loved those cells even when it meant my mother would find some other concoction for me to try next. I mean, i was luckier than most; they never tried to beat the evil out of me abi? I loved my genes oh, even when it meant my father spent more money on hospital bills than school fees when i was growing up, and even though it meant my sister got a little less attention than i did (and i love her for never making me feel bad about that!).
The more i loved the genes, the less they seemed to bother me. And the more i spoke about the genes, the more i found coping strategies. The more i understood the genes, the more i worked around them.
Yes oh, i was the girl in the hospital who would never flinch as they stuck a needle in her arm (I once took fourty eight injections in one famous week), and i was the girl determined to make people laugh because the more they laughed, the less they focused on me and why i was so thin, or why my eyes were yellow!
But as i grew up, i realised that loving but ignoring the cells was not enough. I had to speak up about them. I had to let my friends know that i could hang out with them, but only for this long! And i had to find out from other people living with sickle-cell, what their journey was like! The more i did this, the less it became about me, and the more it became about a nation and a thinking!
Why is sickle-cell practically stigmatised? We should talk about it, and noone should be ashamed to either live with it, or have a family member or friend that lives with it. And why should we deal with it alone when by asking and sharing, we can find more ways of coping with ours? I mean, people have asked me to speak with their friends or family members that live with the disorder but are ashamed or afraid of it, and even though i am not a medical expert, i do enjoy encouraging people!
You can live with sickle-cell. I do. Tope does. Toyin does. Subi does. Jacob does. Tunji does.
Some days, i do not hear from Subomi so i know he has been ill, and i call and we say hello. And vice versa! We are not hiding, and we are not letting our genes stop us from living.
We may not express it the same way, but i think somewhere along the line, we all realised that it really was not how long we lived that mattered, but how well.
Thursday, March 18, 2010
Ten Things to Know about JEANS FOR GENES!
Hi guys!
Here are ten things to note about JEANS FOR GENES, the upcoming fashion party market!
- Jeans for Genes is a fashion show/party and market! IT is scheduled to hold on Sat March 27th, at the swanky SWE BAR, City Mall, Onikan, 3pm.
Jeans for Genes is brought to you by THESE GENES, a sickle cell project run by Tosyn Bucknor. These Genes aims to create awareness-based social programmes, for people to be able to hang out, have some fun, and ultimately, speak and learn about sickle cell disorder.
- The first edition of JEANS FOR GENES held in 2008 and featured lovely designs by Byge, Beampeh and My Q, with music performances by Bez, M.I, Etcetera and so on. (Notice how big they’ve become now?! We saw something back then!)
- This year, JEANS FOR GENES is all about TEESHIRTS! Nigerians love teeshirts, which truly are multi-purpose when you think about it. Teeshirts are used for awareness campaigns, as fashion apparels, and to create a bond. JEANS FOR GENES 2 would like to show what Nigerian designers are now doing with teeshirts on their mind!
- Jeans for Genes is three things in one- an awareness fashion show, which will feature sickle-cell awareness and a fashion show, a teeshirt party with music, drinks (bought by you o), and networking, and a market! Yes o! There will be teeshirts, accessories and more on sale on that day, and the prices will be so good, you’d wish Jeans for Genes was a monthly event!
- It’s JUST a teeshirt right? Not when you see what TONI PAYNE, STRICTLY NAIJA CLOTHING, OUCH! HAPPY FACEZ and IMAGINE CLOTHING do with it! These are five of some of the proudly Nigerian companies whose designs you will see on the runway come Sat Mar 27th! Each of these companies brings something unique to the table, and we are very pleased and excited to have them on board! They have also promised to donate items to the cause, so that proceeds from the sale of same, will go into the final pot at the end of the day!
- The models that will walk the runway will be beautifully made up by LABELLE’s TOUCH. So expect them to look glam! They will also exhibit accessories designed by BUCKSTONE VENTURES, T.T DALK FOOTWEAR, AKIN BEADS, and MY DAZZLE. And everything they model, will be available for sale! (We emphasise that. Forgive us!)
- It’s not just fashion though! We have to have music! And when we say music! We mean an OVERDOSE of music! We mean SKUKI and LOOSE KAYNON, WIZKID and LAMI, ZARA and HAKYM THE DREAM, MODE NINE and SKALES, DIPP and MO CHEDDAH... And the very pretty DOOSHIMA DABO’ADZUANA as the m.c on the day!
- Jeans for Genes is a teeshirt party so OF COURSE, the dress code is TEES AND THESE GENES! The question is... how creative will YOU get with this dress code?! Tees can be dressed up or down, they can be sexy, cute or classic, they can be zany or simple... So which direction are you thinking of going? NIGEZIE, SOUNDCITY,MTV, HIP ON TV, QUEST TV, STV, BELLA NAIJA, GUARDIAN, and more, will be on the Red Carpet, hoping to capture sexy and creative interpretations of the dress code. Remember, its TEES AND THESE GENES!
- But we couldn’t have put this event together without support from s.h.a.r.e, Zapphaire Events, X3M Music, YAT, and our lovely volunteers like Bolaji Ajayi! Youth Are Talking (YAT) will tell us a bit about H.I.V/AIDS so please watch out for their stand, and runway!
- So we do hope we will see you on SAT March 27th at Swe for 3pm, armed with enough cash to bargain shop and your phones to network?! Wait though! Is your name on the guest list yet? Not sure? Well, let me break it down! To get an invite to the Jeans for Genes fashion party/market/show, please get a specially designed THESE GENES teeshirt! There are two style, ‘THESE GENES CELEB’ and ‘ROCK THESE GENES’. The tees are available now and cost N4000! Please call or text 08023066252 to get your name on the Guest List o o o o o o o
So that’s ten things you need to know! Hope to see you there!
Friday, March 12, 2010
Wait A Minute; What is Sickle Cell Disorder?
What is sickle cell disease?
Sickle cell disorder (SCD) is a family of inherited disorders,
of which the most severe and common is sickle cell anaemia
(HbSS). SCD affects how red blood cells carry oxygen around
the body, is a lifelong condition that affects both males and
females, and is the most common genetic disorder in England.
Sickle cell disease can cause fluctuating symptoms ranging
from pain and infection to anaemia and fatigue.
What do sickle cells look like?
Normal red blood cells (see above picture) are disc-shaped,
flexible and can squeeze easily through small blood vessels.
These cells contain haemoglobin which delivers oxygen to where
the body needs it and give the blood cells their red colour.
People with SCD have abnormal haemoglobin. When this
haemoglobin gives away oxygen it sticks together to form long
rods in the red blood cell. These rods become rigid and can
change the red cell from round and flexible to a shape like
a sickle. It is because of this shape that sickled red blood cells
cannot flow easily through small blood vessels. This means the small blood vessels
can get blocked and stop oxygen from flowing.
Who does sickle cell disease affect?
SCD affects mainly people of African and Caribbean descent,
but people from Mediterranean and Asian backgrounds can also
be affected by it.
How many people have it?
There are about 12,500 people with SCD in the UK. It is thought
that the number will increase in the next 10 years.
Why do I need to know about stroke?
Children with SCD are more likely to have strokes than those
without the disease. Of all people with SCD, the risk of stroke is
highest in the most commonly detected type of sickle cell
disease – sickle cell anaemia (HbSS).
The risk of stroke in children with SCD is greatest between
the ages of 2 and 16. About 10% of all children with SCD
will have a stroke by the time they are 20 years old. Stroke
recurrence is also a major concern for children and their families.
Stroke recurs in over 60% of children with SCD.
If you have a child with SCD, make sure you speak to their
doctor about the risk of stroke.
Tips for parents
• If your child has SCD, make sure you speak to their
doctor to find out more about reducing the risks
of stroke and other complications.
• Make sure that the school is aware of your child’s
condition and has drawn up a care plan.
• Provide the school with booklets to explain
what SCD is.
• Make sure family members and teachers are aware
of the signs of stroke and the possible indications
of ‘silent’ stroke.
Tips for teachers
• Be aware of children with SCD in your school and
draw up a care plan.
• Listen to the needs of children with sickle cell, especially
regarding fatigue, dehydration and toilet needs.
• Make sure you are in regular dialogue with parents
of children with SCD.
• Learn the signs of stroke and ‘silent’ stroke. Look out for
changes in behaviour or attention as these may be signs
that a child has had a ‘silent’ stroke
Sickle cell disorder (SCD) is a family of inherited disorders,
of which the most severe and common is sickle cell anaemia
(HbSS). SCD affects how red blood cells carry oxygen around
the body, is a lifelong condition that affects both males and
females, and is the most common genetic disorder in England.
Sickle cell disease can cause fluctuating symptoms ranging
from pain and infection to anaemia and fatigue.
What do sickle cells look like?
Normal red blood cells (see above picture) are disc-shaped,
flexible and can squeeze easily through small blood vessels.
These cells contain haemoglobin which delivers oxygen to where
the body needs it and give the blood cells their red colour.
People with SCD have abnormal haemoglobin. When this
haemoglobin gives away oxygen it sticks together to form long
rods in the red blood cell. These rods become rigid and can
change the red cell from round and flexible to a shape like
a sickle. It is because of this shape that sickled red blood cells
cannot flow easily through small blood vessels. This means the small blood vessels
can get blocked and stop oxygen from flowing.
Who does sickle cell disease affect?
SCD affects mainly people of African and Caribbean descent,
but people from Mediterranean and Asian backgrounds can also
be affected by it.
How many people have it?
There are about 12,500 people with SCD in the UK. It is thought
that the number will increase in the next 10 years.
Why do I need to know about stroke?
Children with SCD are more likely to have strokes than those
without the disease. Of all people with SCD, the risk of stroke is
highest in the most commonly detected type of sickle cell
disease – sickle cell anaemia (HbSS).
The risk of stroke in children with SCD is greatest between
the ages of 2 and 16. About 10% of all children with SCD
will have a stroke by the time they are 20 years old. Stroke
recurrence is also a major concern for children and their families.
Stroke recurs in over 60% of children with SCD.
If you have a child with SCD, make sure you speak to their
doctor about the risk of stroke.
Tips for parents
• If your child has SCD, make sure you speak to their
doctor to find out more about reducing the risks
of stroke and other complications.
• Make sure that the school is aware of your child’s
condition and has drawn up a care plan.
• Provide the school with booklets to explain
what SCD is.
• Make sure family members and teachers are aware
of the signs of stroke and the possible indications
of ‘silent’ stroke.
Tips for teachers
• Be aware of children with SCD in your school and
draw up a care plan.
• Listen to the needs of children with sickle cell, especially
regarding fatigue, dehydration and toilet needs.
• Make sure you are in regular dialogue with parents
of children with SCD.
• Learn the signs of stroke and ‘silent’ stroke. Look out for
changes in behaviour or attention as these may be signs
that a child has had a ‘silent’ stroke
Thursday, March 11, 2010
The TEES are here! YAY!
Great news!
The tee shirts are here!
We would like to thank IMAGINE CLOTHING for working on these tees tirelessly and delivering them on time and on point
We love you!
So!
Remember that these tees serve two purposes
- raise funds for SAMI, our partnered sickle-cell charity
- act as the invite for the event, JEANS FOR GENES!
Jeans for Genes is of course, our fashion show which holds in a few days time. Sat Mar 27th!
Check here http://thesegenes.blogspot.com/2010/03/so-guys-here-is-update-but-first-lets.html for more!
We have two sets of designs!
A} ROCK THESE GENES!
If you would like to declare that you rock your genes, then this teeshirt is for YOU!
black: male (MEDIUM and LARGE), female (MEDIUM)
blue: male (MEDIUM and LARGE)
red: male (MEDIUM and LARGE)
lemon: female (SMALL and MEDIUM)
pink: female (SMALL and MEDIUM)
B} THESE GENES CELEB
This one is for all our every day celebrities! These Genes make you a celeb!
black: female (MEDIUM)
brown: male (MEDIUM and LARGE)
pink: female (SMALL)
red: male (MEDIUM and LARGE), female (small)
And how much do these beautiful teeshirts cost?
( i am glad you asked!)
N4000 (pere!)
N7500 if you buy two at once
N35000 if you buy ten at once
N60000 if you buy twenty at once
and more discounts available!
So now that you are ready to buy and know how much they cost, WHERE do you pick them up from?
We are glad you asked!
(You didnt ask? Sure? Ah well!)
You can purchase a THESE GENES tee in one of three ways!
1. BOOK! PAY! COLLECT!
Book a teeshirt buy paying the amount into an account. Then pick one up!
(pls send a TEXT to 08023066252 to get the account number....)
2. COME! PAY! COLLECT!
Come to any of the collection centres, pay and pick it up!
3. Buy at the gate at the event
THIS IS NOT RECOMMENDED for the ff reasons
- teeshirts would have been sold out by then (we fast and pray)
- teeshirts will cost more then. (hmmn, maybe you should!)
COLLECTION CENTRES
- yaba
- ikeja
- swe (every friday)
for the addresses for yaba and ikeja, pls send text to 08023066252. You see, this IS the internet!
With these few points of ours, we hope we have been able to convince you and not confuse you...
Wednesday, March 3, 2010
So what will you be doing on Sat Mar 27th?
So guys, here is an update!
But first, let's say, its March already?
ALREADY?
This means there are only a few days left to go!
Yes o!
The biggest fashion show/party/market is going down on Sat Mar 27th at the swanky SWE BAR, in Onikan!
Our designers are ready:
TONI PAYNE, STRICTLY NAIJA CLOTHING, OUCH! HAPPYFACEZ and IMAGINE CLOTHING!
See what their designs are like, and buy these tees ON THE SPOT!
Some other designers will also have their gear on sale that day!
Tu Anny
NGUK
And our models will be made up beautifully by LABELLE'S TOUCH!
Recently nominated for a Future Award, this make-up house currently handles on-the-set make up for TINSEL, and also made the models up during the MNET FACE OF AFRICA finale in Lagos!
But what would clothes look like with no accessories?
Well, thanks to BUCKSTONE VENTURES, T.T.DALK FOOTWEAR AND ACCESSORIES, AKIN BEADS and MY DAZZLE, our models will show interesting and cutting edge Nigerian accessories!!!
We. Cant. Wait!
Can you?
(we will all have to wait till the 27th sha)
Just remember to hold enough money on that day to shop!
Clothes! Shoes! Bags! Pictures!
Pictures?
yes o!
Apart from the Red Carpet which is proudly supported by SOUNDCITY, QUEST TV, HIP ON TV, NIGEZIE and more, there will be fashion photogs around to take arty pictures of your friends and yourself!
Imagine coming for the JEANS FOR GENES sickle-cell party and leaving with MORE...especially images to last a lifetime!
All this while being entertained by:
Dipp, Skuki, Lami, S.K.A.L.E.S, Hakym the Dream, Zara, Overdose, Willy Bang, Loose Kaynon, Mo Cheddah and MODE NINE!
YUP!
And this big, wonderful event for purpose, will be hosted by DOOSHIMA DABO'ADZUANA!
Jeans for Genes creates awareness about sicklecell, and this time, will also raise funds to pay some hospital bills!
Jeans for Genes is proudly supported by:
ZAPPHAIRE EVENTS
s.h.a.r.e
X3M Music
SWE
MULTIKRAFT MEDIA
This event is STRICTLY BY INVITATION.
For INVITES, and more information about the event, please check out the blog
www.thesegenes.blogspot.com
join the facebook event page,
http://www.facebook.com/event.php?eid=302889754167
or call
08023066252
07039268846
JEANS FOR GENES 2....
Music! Fashion! Sickle-Cell!
Wednesday, February 24, 2010
Jeans for Genes 2! LETS GO!
On Mar 27th, These Genes will throw the JEANS FOR GENES Music... Fashion...Sickle Cell party!
Featuring designers like
Toni Payne
Strictly Naija
OUCH!
HappyFacez
Imagine Clothing
with music by
Dipp
Skuki
Lami
S.K.A.L.E.S
Hakym the Dream
Zara
Overdose
Willy Bang
Loose Kaynon
Mo Cheddah
There will be teeshirts, accessories and more on sale, plus a runway and photo shoots!
Jeans for Genes creates awareness about sicklecell, and this time, will also try to help a lady living with sickle cell with her hospital bills!
For more information, please check www.thesegenes.blogspot.com
And to book, please send texts to
08023066252
or leave a message here as constant information will be passed on!
You can also join the event page and please check it from time to time
http://www.facebook.com/event.php?eid=302889754167
Monday, February 22, 2010
Fill in the blank space...
and add 'Genes, Jeans and/or Tee shirt' where appropriate
So it's a few weeks to the next 'These Genes' gig and I'm already excited. Overtly so if I may add. Yeah, I'm also asking myself inwardly if everything is alright with me. Guess I'll blame it on my experience at the first gig. They go as follows
1. It remains one of my best networking experience. Even the usually stuck up Lagosians acted normal that day. (might have been the air condition though) Well, most of them are good friends now. (with ME o !!!)
2. (I forgot to add that this list comes in no particular order) The male topless models for Ouch. Hopefully there'll be a repeat perfomance. There's just too much emphasis on females on the runway these days. #Whathappenedtogenderequality?
3. The team . I really can't remember everyone but I do remember there was chemistry . and fun. and positive team work. and patience. at least till I called the wrong set of models for the wrong designer or models when an artiste was on stage . What can I say ? we are human after all. Especially me ;)
4. The models. Almost all of whom were volunteers . I loved the eagerness in their eyes . Their passion. and their determination to conquer the runway (ok, whatever that is !) But honestly, they rocked. Both the amateurs and the pros. and they really conquered the runway !
5. The artistes . If you love to party and have lived in lagos for a second, then you'll know quality gigs don't come cheap. or free for that matter. Except you are a celeb. and after factoring logistics and the cost of trying to look good, it still comes to a stupor. Well, except you are stinking rich. (and in the first place, I was refering to the nobodies like me and not you guys anyways so...)
Back to the gist, the best of the best performed. and I watched them all. FOR FREE . Take this from a wannabe groupie. (I think I'll still write about them later sef ) You never can tell,I might just get more free invites.
6. The sales. For someone who feels window shopping is a balm for the broke, imagine my reaction when I found out that so many prices (of tees, accessories, jeans and other fun stuff) had been crashed for These Genes. Yeah, stoic cheapskate till death !
7. City Mall. I'll state my reasons later
8. ( Once again, remember this list comes in no particular order ) The cause. I feel it is good to help when we can. and I probably would have loved to help more. But seriously, nothing beats fun help. That's my term for helping and having fun at the same time. or on another note, These Genes Volunteering :)
In the past, I have had to volunteer in the sun and under worse conditions. ( This is not me trying to brag or whine o, I am just trying to convince you to volunteer for These Genes o) Especially if you have never volunteered before. Trust me, it's a one in a lifetime offer. (lifetime being 2010)The chances of getting a volunteering job that encourages you to do what you love to do, with people that rock ( I almost said make sense) and in an airconditioned environment is quite slim. Very slim.
and lastly, I lost a little and very bright friend some years ago. We all used to joke that she was way beyond her age, and loved when she asked us grown up questions or acted like an adult. Her energy was overwhelming. She was just five years old, yet you could see the world in her eyes when she spoke. She lit up any room she occupied. and she was an only child . Her first attack did her in.
She was a friend to my little cousins. A daughter to my aunt's and uncle's really close friends.
But her death touched us all and left a scar. and this is just one of many tales. (I'll try to write more soon)
Sickle cell affects everybody one way or the other. Try to make a difference .Do something positive about it.
( say like, buy a These Genes Tee shirt, make a donation , Tell a friend about it or just get involved)
1
So it's a few weeks to the next 'These Genes' gig and I'm already excited. Overtly so if I may add. Yeah, I'm also asking myself inwardly if everything is alright with me. Guess I'll blame it on my experience at the first gig. They go as follows
1. It remains one of my best networking experience. Even the usually stuck up Lagosians acted normal that day. (might have been the air condition though) Well, most of them are good friends now. (with ME o !!!)
2. (I forgot to add that this list comes in no particular order) The male topless models for Ouch. Hopefully there'll be a repeat perfomance. There's just too much emphasis on females on the runway these days. #Whathappenedtogenderequality?
3. The team . I really can't remember everyone but I do remember there was chemistry . and fun. and positive team work. and patience. at least till I called the wrong set of models for the wrong designer or models when an artiste was on stage . What can I say ? we are human after all. Especially me ;)
4. The models. Almost all of whom were volunteers . I loved the eagerness in their eyes . Their passion. and their determination to conquer the runway (ok, whatever that is !) But honestly, they rocked. Both the amateurs and the pros. and they really conquered the runway !
5. The artistes . If you love to party and have lived in lagos for a second, then you'll know quality gigs don't come cheap. or free for that matter. Except you are a celeb. and after factoring logistics and the cost of trying to look good, it still comes to a stupor. Well, except you are stinking rich. (and in the first place, I was refering to the nobodies like me and not you guys anyways so...)
Back to the gist, the best of the best performed. and I watched them all. FOR FREE . Take this from a wannabe groupie. (I think I'll still write about them later sef ) You never can tell,I might just get more free invites.
6. The sales. For someone who feels window shopping is a balm for the broke, imagine my reaction when I found out that so many prices (of tees, accessories, jeans and other fun stuff) had been crashed for These Genes. Yeah, stoic cheapskate till death !
7. City Mall. I'll state my reasons later
8. ( Once again, remember this list comes in no particular order ) The cause. I feel it is good to help when we can. and I probably would have loved to help more. But seriously, nothing beats fun help. That's my term for helping and having fun at the same time. or on another note, These Genes Volunteering :)
In the past, I have had to volunteer in the sun and under worse conditions. ( This is not me trying to brag or whine o, I am just trying to convince you to volunteer for These Genes o) Especially if you have never volunteered before. Trust me, it's a one in a lifetime offer. (lifetime being 2010)The chances of getting a volunteering job that encourages you to do what you love to do, with people that rock ( I almost said make sense) and in an airconditioned environment is quite slim. Very slim.
and lastly, I lost a little and very bright friend some years ago. We all used to joke that she was way beyond her age, and loved when she asked us grown up questions or acted like an adult. Her energy was overwhelming. She was just five years old, yet you could see the world in her eyes when she spoke. She lit up any room she occupied. and she was an only child . Her first attack did her in.
She was a friend to my little cousins. A daughter to my aunt's and uncle's really close friends.
But her death touched us all and left a scar. and this is just one of many tales. (I'll try to write more soon)
Sickle cell affects everybody one way or the other. Try to make a difference .Do something positive about it.
( say like, buy a These Genes Tee shirt, make a donation , Tell a friend about it or just get involved)
1
Labels:
City Mall,
sicklecell,
Swe Bar,
These Genes,
tosyn
Wednesday, February 17, 2010
JEANS FOR GENES needs YOU!!!
JEANS FOR GENES 2... where fashion meets music!
It is a teeshirt and jeans party this time around, and how creative can YOU get?
Inspiration comes from Toni Payne, OUCH and 5ve, with music by Lami, Loose Kaynon, Skuki, S.K.A.L.E.S and Hakym the Dream
More houses to come, more artistes to perform
there will be teeshirts on sale before and on the day, and we are trying to raise money for someones hospital bills!
so lets have a drink, dress our jeans up, take pictures, laugh, and give back!
sickle cell affects everyone directly or indirectly, but some of us still look good in these genes!
By the way, JEANS FOR GENES needs YOU O... if you are
- a photographer
- a videographer
- an accessories designer
- a make-up house
- into pr/promotions/marleting/publicity
- in the media
- a designer
Please send TOSYN BUCKNOR (she wrote this note) a message!
It is a teeshirt and jeans party this time around, and how creative can YOU get?
Inspiration comes from Toni Payne, OUCH and 5ve, with music by Lami, Loose Kaynon, Skuki, S.K.A.L.E.S and Hakym the Dream
More houses to come, more artistes to perform
there will be teeshirts on sale before and on the day, and we are trying to raise money for someones hospital bills!
so lets have a drink, dress our jeans up, take pictures, laugh, and give back!
sickle cell affects everyone directly or indirectly, but some of us still look good in these genes!
By the way, JEANS FOR GENES needs YOU O... if you are
- a photographer
- a videographer
- an accessories designer
- a make-up house
- into pr/promotions/marleting/publicity
- in the media
- a designer
Please send TOSYN BUCKNOR (she wrote this note) a message!
Tuesday, February 16, 2010
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