health technology – Patient Worthy

Source: https://pixabay.com/en/upper-body-lung-copd-disease-944557/

Rare Community Profiles: AlphaID At Home Provides Accessible, Targeted Screening for Alpha-1 Antitrypsin Deficiency (AATD)

Post author:Jessica Lynn
Post published:August 1, 2023
Post category:Alpha-1 Antitrypsin Deficiency Alpha-1 antitrypsin deficiency

Rare Community Profiles Rare Community Profiles is a new Patient Worthy article series of long-form interviews featuring various stakeholders in the rare disease community, such as patients, their…

source: shutterstock.com

Rare Community Profiles: Creating a Caregiver-Centric Social Platform: An Interview with Comend’s Albert Wang and Flawnson Tong

Post author:Jessica Lynn
Post published:April 27, 2023
Post category:Rare Disease

Rare Community Profiles Rare Community Profiles is a new Patient Worthy article series of long-form interviews featuring various stakeholders in the rare disease community, such as patients, their…

source: pixabay.com

ICYMI: Phone Clip-On Can Identify Zika Virus

Post author:Jessica Lynn
Post published:September 16, 2022
Post category:Zika Virus

There are a number of different mosquito-borne illnesses. But sometimes it can be difficult to make an accurate diagnosis when these illnesses – and many others – share similar symptoms…

fancycrave1 / Pixabay

SYDBAT App Can Help with Early Primary Progressive Aphasia Diagnosis

Post author:Jessica Lynn
Post published:July 18, 2022
Post category:Primary progressive aphasia

Primary progressive aphasia (PPA) is a rare neurological disorder and form of frontotemporal dementia which affects one’s ability to communicate. In many cases, people develop PPA prior to turning…

Katheron Intson

Accelerating the Journey to Rare Disease Treatment: An Interview with Katheron Intson of Varient (Pt. II)

Post author:Jessica Lynn
Post published:May 5, 2022
Post category:Rare Disease

Don't forget to check out Part 1 of our interview with Katheron Intson, where we discussed her background, her research experience in GRIN1, and the reasons behind why she developed…

Katheron Intson

Accelerating the Journey to Rare Disease Treatment: An Interview with Katheron Intson of Varient (Pt. 1)

Post author:Jessica Lynn
Post published:May 4, 2022
Post category:GRIN disorder Rare Disease

Katheron Intson is a passionate scientist; she likes understanding how and why things work the way that they do. So when Katheron’s friend reached out about a mysterious health problem,…

Rare Community Profiles: AlphaID At Home Provides Accessible, Targeted Screening for Alpha-1 Antitrypsin Deficiency (AATD)

Rare Community Profiles: Creating a Caregiver-Centric Social Platform: An Interview with Comend’s Albert Wang and Flawnson Tong

ICYMI: Phone Clip-On Can Identify Zika Virus

SYDBAT App Can Help with Early Primary Progressive Aphasia Diagnosis

Accelerating the Journey to Rare Disease Treatment: An Interview with Katheron Intson of Varient (Pt. II)

Accelerating the Journey to Rare Disease Treatment: An Interview with Katheron Intson of Varient (Pt. 1)

Let’s Work Together!

Keep Up to Date

Learn More