Elizabeth Achilles Ndyalusa

Rare diseases may be uncommon, but the people who live with them are extraordinary. They face challenges and struggles that most of us can't even imagine, but they do so with courage, strength, and determination. #rarediseases #rarediseaseday #isupportra…lnkd.in/d76pVHWR

Kwenye uzinduzi wa Miongozo ya Elimu Maalumu na Jumuishi. "Kama elimu inaweza patikana chini ya muembe kwanini isiwe na nyumbani" Balozi Togolani Mavura @tonytogolani

Mheshimiwa Prof. Mkenda, wewe ni kati ya mashujaa uliewezesha watoto wote ambao hawakuweza kupata elimu kutokana na kushindwa kufika mashuleni, leo wanapata fursa sawa na wenzao wanaohidhuria shuleni. Ahsanteni wote pamoja na watumishi wote wa wizara.

Wait! Mtu MWEUSI angevaa pampasi, na sisi WEUSI tungetoka kulalamika Simba waombe radhi? WHITE huyo ni muigizaji, hakulazimishwa, alikuwa kazini katika utafutaji maokoto. TAS na LHRC mlitakaje? WHITE akose pesa ya mboga? Mnashindwa kulaani bandari zinauzwa, mnalalamika ujinga.

Unapofurahia moshi wa shisha, kumbuka unapovuta huo moshi kwa dakika sitini ni sawa na kuvuta sigara 100. …ukikaaa kwenye kijiwe cha shisha, kumbuka na wewe unavuta hata kama huna paipu mdomoni.. Second, third and fourth hand smoking!! @ZakayoMmbaga

Kumbusu Yakuhusu Nini? Picha kuisambaza Na sauti kupaza Ni tendo la kilaza Kumbusu Yakuhusu Nini? Na watoaji povu Kwa kweli ni wachovu Kumbusu si utovu Kumbusu Yakuhusu Nini?

So, let's keep pushing forward together, no matter what challenges come our way. Lupus may try to slow me down, but I'm here to prove that my determination is unstoppable! 💜 #LupusWarrior #LupusAwareness #lupusflares #lupuswarriorstanzania

Remember, setbacks are just temporary roadblocks, not the end of the journey. I'm grateful for the support I have from my loved ones, lupus community (@lupuswarriorstz ) and all of you who continue to inspire me. Your kind words and encouragement mean the world to me! 🙏🏼

Hey everyone, just wanted to give you an update on what's been going on lately. My lupus flares have been making life a bit more challenging, but I refuse to let it stop me from accomplishing my dreams! 💪🏼

I extend my heartfelt appreciation for being featured in #MeetTheFellowWednedday and for all the positive feedback I have received. It encourages me to continue working hard and striving for positive change. I am honored to be part of the #EAEPIAPCohort4…lnkd.in/e3Gumxak

Ahsante sana Balozi @tonytogolani kwa jitihada kubwa unazofanya juu ya kubadilisha mustakabali wa waishio na #MagonjwaAdimu Unaendelea kuwainua na kuwapigania kina Ali na wenziwe. Thank you

@innomangu @JamiiForums Aiseee 🥹🥹🥹

@JamiiForums Ni mawili. Naibu Waziri wa Afya hana uelewa wowote kuhusu bima ya NHIF au uelewa anao, lakini kaamua Kulidanganya Bunge. Kazi ipo.

NAIBU WAZIRI: HAKUNA MADARAJA KATIKA BIMA YA NHIF Mbunge Aida Khenani alitoa hoja kuwa Wananchi wanapokata Bima za Afya wanawekewa ukomo wa baadhi ya Huduma na Dawa wanapofika Hospitali hali inayofanya baadhi waone hakuna umuhimu wa kuwa na Bima hiyo Naibu Waziri wa Afya, Dkt. Godwin Mollel amesema “Eneo la #NHIF hakuna madaraja labda amechanganya na CHF ambapo ndipo kuna madaraja ya kutibiwa kwa kiwango fulani.” Soma jamii.app/NHIFMadaraja #JFHuduma #Governance

This month, we shed light on their journey, challenges, and resilience. Together, let's support, educate, and advocate for a better future. #LetsTalkLupus 💪💜

@paflar @furia_francis Congratulations Prof👏🏾

Congratulations!!

"Kuongozana uelekeo mmoja si kuwa na safari moja. Usione ukadhani!" ~Togolani Mavura.

Even though Lupus Awareness Month has come to an end, our fight against Lupus continues every day. Together, let's keep spreading awareness, advocating for better treatments, and supporting each other on this journey. #LupusAwarenessMonth #lupusawareness @lupuswarriorstz

UGONJWA WA LUPUS: Siku ya Lupus Duniani iliasisiwa na Lupus Canada ambalo ni Shirikisho la Wagonjwa Wanaoishi na Ugonjwa wa Lupus Nchini #Canada Mwaka 2004, na huadhimishwa kila tarehe 10 Mei kila mwaka huku Mei ukitumika kama Mwezi wa kutoa Elimu juu ya ugonjwa huo #LupusAwareness #LupusMonth #JFLupusSpace

Nchini #Tanzania Siku ya Lupus Duniani ilianza kuadhimishwa Mwaka 2021 na maadhimisho haya yalifanyika katika Chuo Kikuu Cha Afya Muhimbili (#MUHAS) kwa miaka miwili ya awali, maadhimisho ya Mwaka 2023 yamefanyika katika Hospitali ya Taifa Muhimbili #LupusAwareness #LupusMonth #JFLupusSpace

Lupus Warriors Tanzania, Chuo Kikuu Cha Afya na Sayansi Shirikishi Muhimbili (MUHAS), Hospitali ya Taifa Muhimbili (MNH) na JamiiForums wameandaa Mjadala na Wataalamu kupitia TwitterSpace kuhusu Ugonjwa huo, Mei 31, 2023, kuanzia Saa 12 Jioni hadi Saa 2 Usiku #LupusAwareness #LupusMonth #JFLupusSpace #JamiiForums

DKT. FRANCIS FURIA (Daktari Bingwa wa Magonjwa ya Figo na Rheumatism MNH na Profesa wa Chuo Kikuu cha Afya na Sayansi Shirikishi Muhimbili): Lupus ni ugonjwa unaoathiri viungo vya mwili kutokana na mashambulizi ya mfumo wa kinga ya mwili kwa viungo ikiwemo, hali hiyo inasababisha hitilafu mwilini na inaweza kuathirika ngozi, moyo, figo, mapafu, mfumo wa fahamu, damu na misuli Mgonjwa anaweza kupata athari kwenye mfumo zaidi ya mmoja au mifumo yote ya mwili kuathirika #LupusAwareness #LupusMonth #JFLupusSpace #JamiiForums