Antonio Ochoa

@farm_vizcaino Has probado a ofrecerles un colirio homeopático? 😂😂😂 para eso no necesitan recetas🤪🤣🤪🤣🙃

Y siempre compra esa pomada y se le quita. Porque le pasa mucho. En cuanto le digo que lo mismo le pasa mucho por usar un antibiótico sin control ya recula y no, no le pasa mucho, le pasa una o dos veces al año. O menos.

Llevo dos consultas en media hora de guardia. Un diclofenaco colirio sin receta porque se lo echa cuando le duele y no ve y siempre se lo dan sin receta (trae la caja con el cupón precinto). Una oftalmolosa aureomicina porque viene la hija de camino y le ha salido un orzuelo.

We have announced the results of the inaugural elections for the three National Pharmacy Advisory Councils in England, Scotland and Wales. Meet the newly elected members and find out more: bit.ly/4uqEOWj

Voting has now closed. Thank you to members who voted and helped shape the first National Pharmacy Advisory Councils for the future Royal College of Pharmacy.

The inaugural elections for the Royal College of Pharmacy close 5pm on Wednesday, 11 March. Make your vote count and help create the National Pharmacy Advisory Councils for the new royal college. Vote now: ow.ly/Owmm50YlN2h

Professor Claire Anderson, RPS President, comments in The Guardian on new research exploring whether GLP-1 medicines may influence brain pathways linked to addiction, highlighting the need for further clinical trials. Read more: ow.ly/owoE50YpFhB @denis_campbell @guardian

Do you work in the pharmaceutical industry or need to know more about drug manufacturing? Join our 3-day Tabletting Technology Course led by industry experts for hands-on practical sessions: ow.ly/rfEu50Yn0Bz @pittkendal @IHollandTooling

Voting is open for the Royal College of Pharmacy elections. Cast your vote to help create the National Pharmacy Advisory Councils in your nation. Vote now: ow.ly/Owmm50YlN2h

Thank you for joining us on this takeover during #RareDiseaseDay, and a shoutout to Rare Revolution Magazine for giving us the space to highlight rare liver diseases and for their incredible work advancing the rare disease community. If you or a loved one are navigating a rare liver disease, you’re not alone. Finding a community that understands can make all the difference. At GLI, our Advanced Advocacy Academy (A3) features training programs and advocacy opportunities for patients and caregivers who want to become advocates. Join the movement, share your story, and learn more about our work by visiting: globalliver.org/advanced-advoc… #RareAware #RareLiverDisease #A3experience #liverhealth #rarediseaseday

La Traumatóloga Ines Moreno, que hace unos tuits geniales y muy didácticos, se suma al #DiaMundialEnfermedadesRaras con un tema mas que importante, el tratamiento farmacológico de las #EERR, los #MMHH (@aelmhu), marcados por el aspecto económico. Gracias por su trabajo👏👏#RareDiseaseDay 💚💜

Cockayne syndrome (CS) and Trichothiodystrophy (TTD) are ultra-rare genetic conditions caused by defects in the nucleotide excision repair (NER) pathway. While each condition is unique, they share overlapping biology and care challenges. Our Year of the Zebra video focuses on CS as one example within this rare group. #RareDiseaseDay #CockayneSyndrome #DNRRepairDisorder #RDD #RDD2026 #CS @Share_Care_Rare youtu.be/C6Aq6DK8QSA?si…

Naomi doesn't have HFI, but lives with 5 siblings who all do have HFI. She explains how her older sister has sustained liver damage because HFI was not diagnosed. It is vital for the lives of children born with HFI, that they are diagnosed before liver damage starts. At HFI support UK, we are working to get a neonatal screening test for HFI to become routine. We rely on donations to keep HFI support going. Please contribute if you can. Donation link on our website. #rarediseaseday #raisingawareness #hfiawareness #nosugar hfisupport.org.uk

#RareDiseaseDay | Hoy, en el Día Mundial de las Enfermedades Raras, recordamos que 300 millones de personas en el mundo viven con una enfermedad rara. No son cifras, son vidas que exigen diagnóstico oportuno, tratamiento continuo y decisiones reales. La rareza no puede ser invisibilidad. #28Febrero #EnfermedadesRaras #FECOERSomosTodos

🧬 What is MPS? Mucopolysaccharidoses (MPS) are rare, inherited disorders that prevent the body from breaking down certain sugars, causing progressive damage to the body and brain over time. Learn more: mpssociety.org/en/learn-about… @mpssociety

Pharmacists are at the heart of improving awareness and care for people living with rare diseases. Join this webinar to explore the realities of rare disease care: ow.ly/UprQ50XXZFC @afocoa @weareMSUK

Pharmacists are at the heart of improving awareness and care for people living with rare diseases. Join this webinar to explore the realities of rare disease care: ow.ly/UprQ50XXZFC @afocoa @weareMSUK

The 28th February is International Rare Diseases day, I’m very grateful to the @rpharms for organising this event to increase awareness among pharmacists about people living with rare diseases

@PabloCamPiq El coste de $15m/paciente por 50 años de esperanza de vida. Hay otros tratamientos, como por ejemplo Elaprase (idursulfasa) para MPS2, a igual esperanza de vida de coste similar aprobados en servicios públicos de salud como el NHS en Reino Unido desde hace más de una década

🔴 Atención a este supuesto médico jubilado (según él mismo) Ante la petición de Leo para tener acceso a un medicamento que mejoraría notablemente su vida (tiene una enfermedad terrible), este tipo dice que es muy caro. Esto me lo encontré en el Congreso con medicamentos contra el cáncer. Tenemos para pagar todo tipo de basura ideológica en el exterior, cientos de millones de € para el cine y asesores, pero este “médico” dice que reducir el sufrimiento de enfermos es “caro”. Terrible.

Pharmacists are at the heart of improving awareness and care for people living with rare diseases. Join this webinar to explore the realities of rare disease care: ow.ly/UprQ50XXZFC @afocoa @weareMSUK

😔 The UK National Screening Committee decided AGAINST #newbornscreening for Metachromatic Leukodystrophy, despite promising pilot programmes in Europe and caregiver surveys showing median diagnosis delays of ~1 year with rapid decline💔🧬 …eening-recommendations.service.gov.uk/metachromatic-…

@IhabFathiSulima @Info_Rares Fabry

What is the diagnosis?