PATIENT ADVOCACY Archives - chandler crews

wind in my hair, I was there

Jun 21, 2022 • ACHONDROPLASIA, CHICAGO, CONFERENCES, RESEARCH

wind in my hair, I was there

ellie simmonds: a world without dwarfism

Apr 1, 2022 • ACHONDROPLASIA, LIMB LENGTHENING, NEWS, PHARMACEUTICAL, RESEARCH

ellie simmonds: a world without dwarfism

rare disease day • 2022

Feb 28, 2022 • ACHONDROPLASIA, PATIENT ADVOCACY

rare disease day • 2022

dwarfism awareness day • 2021

Oct 25, 2021 • ACHONDROPLASIA, LIMB LENGTHENING, PATIENT ADVOCACY

dwarfism awareness day • 2021

achondroplasia research conference | 2021

Jul 12, 2021 • ACHONDROPLASIA, CONFERENCES, LIMB LENGTHENING, PATIENT ADVOCACY, PHARMACEUTICAL, RESEARCH, SURGICAL

achondroplasia research conference | 2021

Apr 24, 2021 • ACHONDROPLASIA, LIMB LENGTHENING, NEWS, PHARMACEUTICAL

born small

Rare Disease Day 2021

Feb 28, 2021 • ACHONDROPLASIA, PATIENT ADVOCACY

Rare Disease Day 2021

What Matters to Me

Feb 21, 2021 • ACHONDROPLASIA, PATIENT ADVOCACY

What Matters to Me

Rare Disease Day on Capitol Hill

Feb 29, 2020 • ACHONDROPLASIA, PATIENT ADVOCACY

Rare Disease Day on Capitol Hill

Food and Drug Administration

May 12, 2018 • ACHONDROPLASIA, PATIENT ADVOCACY

Food and Drug Administration