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Press Release - Sen. Pia Cayetano's sponsorship speech of Senate Resolution No. 806

Press Release - Sen. Pia Cayetano's sponsorship speech of Senate Resolution No. 806
senate.gov.ph - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from senate.gov.ph Daily Mail and Mail on Sunday newspapers.

Pia cayetanoPambansang alagadCarmencita padillaNational scientistUniversity of the philippines dilimanOrder of national scientist award ordenOrder of national scientist awardChairperson of the committee onCarmencita padilla as national scientistSenate resolution noPhilippine genome centerSenate resolutionNational scientist awardPhilippines dilimanNewborn screening actNewborn screening bill

Press Release - TRANSCRIPT: Sen. Pia Cayetano's privilege speech on Rare Disease Day

Press Release - TRANSCRIPT: Sen. Pia Cayetano's privilege speech on Rare Disease Day
senate.gov.ph - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from senate.gov.ph Daily Mail and Mail on Sunday newspapers.

The philippinesPia cayetanoJuan magdaraogSchan lieamSonny angaraZiah nicoleLouise franzineNational scientistGood healthNational rare disease weekWorld health organizationSustainable development goalsRare diseaseRepublic actRare diseasesRare disease act

'Rare disease law funding remains inadequate'

Seven years after the passage of a law seeking to help Filipinos with rare diseases, the funding for Republic Act 10747 or the Rare Disease Act remains inadequate.

University of the philippinesQuezon cityVictor andres manhitAlvin manalansanNational institutes of healthHealth careStratbase albert del rosario instituteRepublic actRare disease actUniversal health care watchStratbase albert del rosarioGeneral appropriations actNational institutesAndres manhit

Healthcare experts seek more funds under Rare Disease Law

Seven years after the passage of a law meant to help Filipinos with rare sometimes called orphan – diseases, implementation and funding remain inadequate, and only a holistic approach will ensure that patients can get help for early detection and treatment.

University of the philippinesQuezon cityAlvin manalansanVictor andres manhitRare diseases management program strategic planNational institutes of healthPhilippine society of orphan disordersHealth careStratbase groupBalancing prioritiesRare disease actUniversal healthcare watchPhilippine societyGeneral appropriations actNational institutesUniversal health care

A fair share for patients living with rare diseases - BusinessWorld Online

A fair share for patients living with rare diseases - BusinessWorld Online
bworldonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from bworldonline.com Daily Mail and Mail on Sunday newspapers.

Manuelv vallesterosLourdes desiree cembranoAlvin manalansanMarita tolentino reyesVictor andres dindo manhitCeleste mae campomanesCarmencitad padillaCouncil on occupationalMaternal healthBureau childChairperson of the health technology assessmentHealthcare association of the philippinesPhilippine college of chest physiciansUniversity of the philippines manilaRare disease management program planAdvisory council