taiba rare

Reflecting our #commitment to patients, we continue to focus on access to #health for #patients in our region to reach those in need of our #medicines. At #taibaRare we hope to achieve life changing benefits for #RareDisease patients in the #MiddleEast and #Africa. It's all about #UnlockingAccessToRare. #accessrare #Wearetaiba #taibarare #accessrare #mena #gcc #healthawareness #orphandrugs #mea #oman #ksa #uae #qatar #kuwait #bahrain #pharmaceutical #iraq #lebanon #jordan #egypt

#FabryDisease is more than a diagnosis—it’s a daily challenge for individuals and families coping with its effects. This lysosomal storage disorder, caused by a deficiency of the enzyme alpha-galactosidase A, leads to the accumulation of globotriaosylceramide (GL-3) in the body’s cells. Symptoms and Impacts: • Chronic pain, especially in the hands and feet. • Gastrointestinal issues, including abdominal pain and diarrhea. • Cardiovascular and kidney complications, often leading to significant organ damage if untreated. Coping Strategies: • Enzyme replacement therapy (ERT) helps manage symptoms and slow progression. • Support groups provide emotional and psychological support for patients and caregivers. • Specialized care teams, including cardiologists, nephrologists, and geneticists, play a critical role in comprehensive management. Living with Fabry Disease requires resilience and access to proper care, but with increased awareness and advancements in treatment, the outlook is improving. #taiba #rare #taibarare #accessrare #rarediseases #lysosomalstoragedisorders #fabrydisease #genetichealth #healthmatters

#SickleCellDisease (#SCD) is a genetic blood disorder that affects hemoglobin, causing red blood cells to assume a rigid, sickle-like shape. These cells can block blood flow, leading to pain crises, organ damage, and an increased risk of infections. In the GCC, SCD is a significant health concern: Oman has a relatively high carrier rates, with 6%-10% of the population carrying the gene. Bahrain and Saudi Arabia also report notable prevalence rates due to high consanguinity in these regions. Efforts to combat SCD in the GCC include: • Newborn screening programs: Early detection is vital for managing the disease. • Genetic counseling: Encouraging informed family planning decisions. • Advanced treatments: Hydroxyurea and bone marrow transplants offer improved outcomes. Raising awareness about SCD is crucial for improving quality of life and ensuring access to innovative treatments for those affected. #taiba #rare #taibarare #accessrare #rarediseases #sicklecell #gcchealth #genetichealth #blooddisorders

في هذا اليوم، نحتفي برؤية حضرة صاحب الجلالة السلطان هيثم بن طارق، التي تلهمنا جميعًا لتحقيق الازدهار والرخاء لوطننا العزيز. كل عام وعُمان وأهلها في تقدم ورخاء. فلنستمر معًا في خدمة مجتمعنا وتعزيز جودة الحياة للجميع. 🇴🇲 🇴🇲

#WilsonDisease is a rare genetic disorder that disrupts the body’s ability to process copper, leading to toxic accumulation in organs like the liver, brain, and eyes. It’s caused by mutations in the ATP7B gene, which affects the transport of copper in cells. Symptoms can vary greatly and may include: • Liver issues: Jaundice, fatigue, or acute liver failure. • Neurological effects: Tremors, difficulty walking, speech problems, and personality changes. • Kayser-Fleischer rings: Copper deposits around the cornea, visible during an eye exam. Diagnosis often involves: • Blood and urine tests to measure copper levels. • Genetic testing to identify ATP7B mutations. • Liver biopsies in certain cases. Wilson Disease is manageable when detected early. Options include medications like chelating agents that remove excess copper, zinc therapy to block copper absorption, and dietary modifications to limit copper-rich foods like shellfish, nuts, and chocolate. In severe cases, a liver transplant may be necessary. #taiba #rare #taibarare #accessrare #rarediseases #genetichealth #liverhealth #neurologicaldisorders

Happy new year! 🤩🎉 #taiba #taibarare #accessrare #newyear #2025

As 2025 dawns, taiba renews its commitment to providing exceptional care and support for all. Let this year bring health, happiness, and hope to every family. Happy New Year!🤩 🤩

#NiemannPickDisease Type C (#NPC) is a rare and progressive #geneticdisorder that affects the body’s ability to transport #cholesterol and lipids within cells. This leads to their accumulation in various organs, including the #brain, #liver, and #spleen. Symptoms can include #movementdisorders, #cognitivedecline, and #jaundice in infants. NPC is often called "childhood Alzheimer’s" due to its severe neurological impact. Early #diagnosis and specialized care are essential to manage symptoms and improve quality of life, though current treatment options are limited. #taiba #rare #taibarare #AccessRare #NPCAwareness #GeneticDisorders #LipidMetabolism #PatientSupport #NeurologicalCare #HealthMatters

🇶🇦 Taiba Rare celebrates Qatar National Day with pride! On this special occasion, we honor the resilience, unity, and achievements of Qatar, wishing its people and leadership continued success and prosperity. 🌟 🇶🇦 شركة طيبة رير تهنئ دولة قطر وشعبها الكريم بمناسبة اليوم الوطني. في هذا اليوم المميز، نحتفل بقيم الوحدة والازدهار التي تجعل قطر رمزًا للفخر والتميز. نتمنى لكم دوام التقدم والنجاح! 🌟 #taiba #Rare #AccessRare #Qatar #QatarNationalDay #TaibaRare #RareCare #اليوم_الوطني_القطري

#DistalRenalTubularAcidosis (#dRTA) is a rare #kidney disorder that impairs the ability of the kidneys to properly excrete acids into the urine, leading to an imbalance in the body's #pH levels. Symptoms include #fatigue, #bonepain, #kidneystones, and growth delays in children. dRTA can be inherited (genetic) or acquired due to other conditions like autoimmune diseases. Early #diagnosis and treatment—often involving #alkalinetherapies to restore pH balance—are crucial for preventing complications like #osteomalacia (soft bones) and #chronickidneydisease. #taiba #rare #taibarare #AccessRare #dRTA #KidneyHealth #MetabolicDisorders #PatientCare #RareDiseases #HealthAwareness