Joined December 2023
- Tweets 68
- Following 46
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Pinned Tweet
May 11
What happens when you bring #sicklecell care closer to people? They come.
Next week I’m visiting #Bulondo Health Centre in #Kanduyi Subcounty, where I serve as Medical Officer of Health.
A Level 3 facility that started with 5 patients. Today: 100 .
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Jun 15
#Sicklecell and poverty don't just coexist. They feed each other.
Malnutrition. Cold housing. Chronic stress. Dehydration. Each one, a crisis trigger, and together, a cycle that's almost impossible to break.
Read full post👇tinyurl.com/SickleCellAndPov…
#SickleCellEquityKE
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Jun 12
Doses get missed because pharmacies run out, refills are unaffordable & #systems fail families.
Patients sometimes have to choose between survival, #medication & food. Or they're just exhausted from years of daily pills.
Full post: tinyurl.com/MissedDoses
#SickleCellEquityKE
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May 11
What happens when you bring #sicklecell care closer to people? They come.
Next week I’m visiting #Bulondo Health Centre in #Kanduyi Subcounty, where I serve as Medical Officer of Health.
A Level 3 facility that started with 5 patients. Today: 100 .
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May 11
But Bulondo has significant gaps: no hemogram machine, no U/E/Cr testing, and limited monitoring capacity.
Patients come for clinical care, then travel AGAIN to the nearest lab for tests, then return with results.
Multiple trips. Multiple costs. Multiple barriers.
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May 11
This proves Primary Care Networks work - but also shows what happens when we build access without capacity.
→ May 14th, I’m documenting #sicklecell patient journeys. I’ll share their stories.
Want to support this program? DM me.
Read dull post: tinyurl.com/SupportBulondo
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What a child with #sicklecell wants you to know.
To friends and their parents: Your kindness matters.
But sometimes, the way you try to protect ends up isolating instead.
Here’s what children with sickle cell want, even when they don’t know how to say it:
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They don’t want to be treated like they’re fragile. When you’re too careful, they feel like the sick kid everyone has to be gentle with.
They want normal friendship: teasing, inside jokes, competition. Include them in original plans, not watered-down “safe” versions.
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What they need: inclusion as default, water/shade available (not forced), permission to step out without drama, trust when they say they’re fine.
Full post 👇
tinyurl.com/WhatAChildWithSi…
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New term, new teachers. The explanations start all over again.
It’s May. Schools are opening. For families managing sickle cell, this means starting from zero.
New teachers who don’t know your child. New classmates. New staff to educate on #sicklecell.
Every single term.
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What we need: standardized health handovers when teachers change, school-wide chronic illness policies, trained matrons in boarding schools.
Until then, families start over every term.
Read full post: tinyurl.com/NewSchoolTerm
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Apr 30
Last week I wrote about how teachers who don't understand #sicklecell make school impossible.
You asked: WHAT's the solution?
Here's what works:
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Apr 30
School #healthofficers trained on #sicklecell - know warning signs, when to call parents vs ambulance, basic pain management
Communication systems - parents, teachers, healthcare providers talking regularly, not just in emergencies
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Apr 30
Right now, success depends on luck:
Understanding teacher? Sympathetic headteacher? Parent who can advocate?
With #policy, children don't choose between #health and education. They can do BOTH.
→ Read full post on LinkedIn👇tinyurl.com/SickleCellSchool…
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Apr 27
Teachers who don't understand #sicklecell can make school impossible for a child.
A child misses 2 weeks because of a crisis. Returns. Teacher says: "You've missed too much. You'll repeat the term."
No empathy or catch-up plan. Just judgment.
This happens too often.
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Apr 27
What good teachers do:
1/ Ask "What do you need to succeed?"
2/ Create catch-up plans after medical absences
3/ Allow children to sit out PE without shame
4/ Communicate proactively with parents
5/ Educate classmates so accommodations aren't seen as "special treatment"
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Apr 27
Schools need:
Ongoing teacher training, clear policies on makeup exams/modified PE, health officers who understand sickle cell, and communication systems connecting parents/teachers/providers.
Education is a right, not a privilege.
Full post: tinyurl.com/TeachersAndSickl…
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