Audrey Sickle Cell Foundation

Audrey Sickle Cell Foundation Dedicated to helping Sickle Cell Warriors live productive lives and creating awareness and educating people about the disorder.

Auntie Tee like I fondly call you   this is a huge vacuum, yes you fought really hard and that's my only consolation. Wh...
13/05/2026

Auntie Tee like I fondly call you this is a huge vacuum, yes you fought really hard and that's my only consolation. When I started Audrey Sickle Cell Foundation I was modeling after your organization SAMI and that of others; I can't even find the right words, we were in the same hospital during my surgery and all you did was encourage me... The sickle cell community has lost a GENERAL... your absence would be felt. You stood strong despite all the shenanigans Sickle Cell threw at you, your legacy lives on

This picture was you cheering Us on after our genetic counselling training in 2019 ... Mama we surely miss you.

Sun re o Auntie Tee



09/05/2026

Big shout-out to my newest top fans! Oritsegbubemi Ogungbe

Hello fam, June 19 is here!!!!We're grateful for your unwavering support in our mission to improve the lives of individu...
07/05/2026

Hello fam, June 19 is here!!!!

We're grateful for your unwavering support in our mission to improve the lives of individuals affected by Sickle Cell Disorder (SCD). Your contributions have made a significant impact, and we appreciate your dedication.

As we look towards *June 19, 2026* (World Sickle Cell Day), we invite you to join us by volunteering or providing financial support. Together, we can create a brighter future for those living with SCD.

Thank you again for your kindness and commitment to humanity, through Audrey Sickle Cell Foundation (ASCF). May your generosity be rewarded with abundant blessings.

Together, let's make a difference.

Best Regards,

Kola Elijah,
Executive Assistant

Cc

Audrey Mukoro
Founder, ASCF



Hello May...Please be kind to all our warriors, donors, partners, supporters, volunteers and our founder.
03/05/2026

Hello May...
Please be kind to all our warriors, donors, partners, supporters, volunteers and our founder.

20/04/2026

This right here is the reality of our beneficiaries, this is the reason why we do what we do for our underprivileged sickle cell warriors even when we are burnout

In running our organization over the last 8 years, we are met with impoverished families struggling to keep up with decent meals and the medical care for their wards and for this reason we're doing our best to continually commit to helping them to the best of our ability.

If you are moved to be a beacon of hope kindly reach out and together we can make a whole lot of difference to our beneficiaries whilst helping them stay healthy.

šŸŽ„Dr.

Did You Know 1. Your tongue is the main culpritMost bad breath comes from bacteria on the tongue—not your teeth. If you’...
17/04/2026

Did You Know

1. Your tongue is the main culprit
Most bad breath comes from bacteria on the tongue—not your teeth. If you’re not cleaning your tongue, you’re missing the source.
2. You’re not flossing
Food and bacteria trapped between teeth break down and create odor—even if your teeth look clean.
3. Tonsil stones (tonsilloliths)
These are small, calcified debris in the tonsils that smell extremely foul and are a VERY common cause of chronic bad breath.
4. Dry mouth (xerostomia)
Saliva helps wash away bacteria. If your mouth is dry—especially overnight—odor-producing bacteria build up fast.
5. Post-nasal drip
Mucus from allergies or sinus issues can drip into the throat and feed bacteria that produce bad odors.
6. Gum disease (periodontal disease)
Inflamed or infected gums harbor bacteria that produce strong, persistent bad breath.
7. Sinus infections
Chronic sinusitis can produce thick, infected mucus that contributes to a foul smell from the back of the nose and throat.
8. Acid reflux (GERD or LPR)
Stomach contents coming up into the throat can create a sour or unpleasant odor—even without classic heartburn.
9. Certain foods and diets
Garlic, onions, high-protein or low-carb diets can change how your breath smells from the inside out.
10. Underlying medical conditions or medications
Diabetes, liver or kidney issues, and certain medications can all affect breath odor by altering body chemistry or causing dry mouth. They can also alter the way your body filters toxins.

Dear Sickle Cell Warriors, never ever settle for less, that you have a health disorder isn't enough to accept anyone who...
15/04/2026

Dear Sickle Cell Warriors, never ever settle for less, that you have a health disorder isn't enough to accept anyone who isn't deserving of your attention, it's better to wait for the right person at the right time than to shoot yourself in the foot.

Yes you have SCD, what is the big deal about that? You didn't bring it upon yourself and that should not make you drop your standards or accept the barest minimum. Live intentionally, take care of yourself, no need for self pity, when down nurse yourself and get back better; it's not easy yes but keep showing up and pushing. When it's time you'll get someone who deserves you.

The story below is from one of my cell sisters who permitted I share her story, she finally got a kind partner whom she had desired all the time, she's had a fair share of wrong men too before meeting her Prince charming.

Read her story below šŸ‘‡

I’ve never been in a relationship with a man that takes care of me the way Bae does. Guys I’ve dated in the past either went into panic mode when I got sick (which I understand when you aren’t use to this life) or I’ve had to beg for a visit in the hospital.

Even though my support system is amazing, I’ve gotten use to being in the hospital by myself. Sometimes I need that break anyway.

But Bae stayed with me both nights at the hospital last week, waking up in the middle of the night either to rub my back before the surgery or to help me to the bathroom after surgery. He helped sanitize my body from head to toe to prep for surgery, prayed over me before leaving for work the day of surgery, helped me walk around the nurses station (I’ve been advised to walk since I got out of surgery) and was there literally within 5 minutes to pick me up when I got discharged. He’s made sure I’ve eaten healthy low fat meals as the doctor ā€œprescribed.ā€

He told me he enjoys taking care of me and it shows. If I’m in his presence, you guys can rest assured I’m not doing too much (or anything at all) and actually resting. (He actually checked me when he thought I was on a work call yesterday. Lol.)

I’m soooooo grateful and appreciative to have him in my life and actually understand my sickle cell struggle cause he’s been there (he was cured of it over 20 years ago).

Before Jenn passed away, we talked about me opening up in order to obtain the relationship I needed and wanted. I was mad, hurt, and probably bitter because of my dating experience and had shut people out.

Bae is absolutely the best. He was indeed patient while I worked through my emotions as it pertained to intimate relationships. The timing of when we switched from being friends to being romantic partners could not have come at a better time.

He is definitely my man crush not just today, but everyday.

Love you beyond the moon and stars!! šŸ˜šŸ’‹šŸ˜šŸ’‹

PS: Ain’t no April Fool about this one.












AVN and Tram Dependency!!!Our founder shares her story on AVN and Drug dependency, read below šŸ‘‡ How my Avascular Necrosi...
13/04/2026

AVN and Tram Dependency!!!
Our founder shares her story on AVN and Drug dependency, read below šŸ‘‡

How my Avascular Necrosis and tram dependency started, I had a severe crisis episode the type that landed me in a government hospital for weeks, I was admitted for malaria , acute Chest syndrome and lower back crisis. I was there for 3 weeks and some days. During the admission the medical team monitored me closely because of ACS and low blood levels, I was on oxygen for a few days, almost a week before the ACS got better.

The team tried all they could to manage my bone crisis, they did all they could do for me, for the 3 weeks plus on admission, the pains started on my lower back, butt and left hips but I didn't take it seriously then because I had to maintain my job as a classroom teacher so whenever it starts I'll just pop in my pain meds and continue teaching because the fear of my employer was the begin of wisdom, each time this pain came up I suppressed it with tram which was the painkiller I was given in the hospital, little did I know that I was getting a relief and also digging a grave.

That was a job I just started and it was a demanding, being a Montessori teacher then was a flex, it was a job I got on merit, a big school then and owner wasn't bothered about my health because I told her during the interview and she really didn't mind especially because I was equal to the task and aced the oral and class interview; so I did everything to make sure my health didn't interfere with my job because I told her I would be able to cope.

So imagine what would happen if I didn't mask the pains and took excuses weekly, definitely I'd have been replaced and so I had to keep up, in Montessori settings, as a classroom teacher your sitting time was minimal and so that's how my long hours of standing and teaching was causing me severe lower back crisis and also left Avascular Necrosis pain, I managed it closely by popping tram pills for almost 3 terms till my body finally broke down and I landed in the hospital for 3 weeks plus, at this point I had no option but to quit the job I was over protective off, even when I was finally discharged from admission the pain on that hip lingered for 2 years up on till I was referred to an orthopedic surgeon who said I was dealing early stages of Avascular Necrosis, because at some point I started limping, I could no longer wear heels, it had to be flats.

The surgeon sent me for physiotherapy, which I was now doing 3 times a week for almost a year and gradually I stopped limping and got back my mobility but in the cause of trying to maintain my job and make a living for myself as a young lady and protecting my job I was putting my own health in jeopardy which graduated into complications and drug dependency.

I became very dependent on tram and was over protective of my job and I stretched my body beyond it's limits which almost caused me my left hip, thankfully I haven't gone too deep on the tram dependency and the AVN got better with each therapy session but it was a lot and my doctor had to change my pain meds and weaned me off tram dependency.

Dear Warriors, Please always listen to your body before it gets too late... A stitch in time saves nine. Reach out to Us Audrey Sickle Cell Foundation via DM if you are dealing with painkiller dependency.

l or

Happy birthday bro, keep defeating sickle cell disorder. May God continue to bless you immensely for all you do. Cheers ...
07/04/2026

Happy birthday bro, keep defeating sickle cell disorder. May God continue to bless you immensely for all you do. Cheers to more šŸ™

Sharing our founder's experience Some people say I'm proud, some say I intentionally don't respond or pick up calls. For...
03/04/2026

Sharing our founder's experience

Some people say I'm proud, some say I intentionally don't respond or pick up calls. For a very long time now, ( as far back as 2017/ 2018) my mobile phones, tab and even laptop haven't rang out. When people call me, my phones just lights up and if I wasn't there when the lights came up, I return the missed calls if necessary. My folks/friends already know this about me, it's much easier to reach me on WhatsApp than to call directly.

The reason is because the vibration or ring tones gives me panic attacks/ anxiety besides this I also react to unexpected noises especially sounds like knockouts, car honks etc they make my heart race more than normal.

These panic attacks/anxiety triggers pain episodes for me and before you know it I'm having full pain episodes. For me it's even worse with vibrations and unexpected noise. My little daughter already knows that I don't like noise, and Incase you're wondering if I listen to loud music yes I listen to loud music in fact if it's not loud, I don't enjoy it, my headset has the volume above average; at home the home theater is also loud to the level I can absorb.

If I'm to go out to a noisy place either church, market or crowded places I prepare for it mentally, and try as much as possible to do what I need to do and get back to my comfort zone.

For those who say it's pride or I'm ignoring you intentionally pls kindly understand that it's not what you are thinking, it's just me protecting myself or health like doctors have advised. And if I missed your calls it's easier to send a text or WhatsApp message or you wait for me to return the missed calls.

BTW: Pictures from our free Sickle Cell Clinic held in December 2025, God continually bless Us and our donors to continually make this Free Clinic a reality.



Warriors This is why we stopped sending money to warriors directly, in the almost 8 years of running Audrey Sickle Cell ...
01/04/2026

Warriors

This is why we stopped sending money to warriors directly, in the almost 8 years of running Audrey Sickle Cell Foundation we have encountered a lot of such especially in the earlier time we started the organization. Some even plan with the hospital or medical professionals who are fraudulent to act and even falsify test results. In 2020 - 2021 my team and I concluded that no more, if you need help and we can't verify your claims you won't get any money from Us and that's how they started calling Us unprintable names.

Most of the time we use our personal funds, not like we have millions stacked up somewhere, we go out of our way to help only to discover we've been played. Several times donors make their own enquiries too and even go as far as requesting for proofs too, because of the trust they have in Us, they keep supporting the work we do.

Below is the experience of my cell sisters, last night and to think she squeezed herself to provide the help, what level of wickedness is this? Read below šŸ‘‡

In the early hours of yesterday morning, I responded to what was presented as an emergency involving a sickle cell warrior 29 y/o reportedly in priapism, needing urgent support to get to the hospital.

Despite my own very limited means, I made a personal sacrifice to send money immediately, because in situations like that, time is critical and every second counts.

I later went to the accident and emergency ward where he claimed he has been admitted to follow up.I was told no one presented with the case. This is deeply concerning!

As advocates, many of us are not operating from abundance. We give, we stretch, we sacrifice, because we genuinely care about the lives of fellow warriors. But situations like this are not just disappointing, they are damaging.

To everyone within the sickle cell community, please understand this:False alarms and deception do not just take money, they erode trust, drain already limited resources, and can delay help for those who are truly in life-threatening need.

This must stop! At the same time, this is a reminder for all of us in the advocacy space, compassion must be paired with structure.

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