google-site-verification: google39d92523271df308.html Interview With Dr Ruth Napier - Rare Disease Expert and Immunologist - The Axial Spondyloarthritis Podcast

Episode 187

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Published on:

29th Oct 2023

Interview With Dr Ruth Napier - Rare Disease Expert and Immunologist

In this episode I interview Dr Ruth Napier, a rare disease and Immunologist who is studying Axial Spondyloarthritis. We discusses the research Dr Napier is doing regarding genetics and AS. As always, this is designed to help you increase your knowledge of AS. Here is a link to the discussing the research on mice and Card9.

Here is a link to Dr. Napier's lab page.

To make a donation to Dr. Napier's Lab and fund her research, click here.

Here are the links to the YouTube channels for:

Yoga for AS

Alex Levine, Fitness Alex's Full Workout Video

All the below links are affiliate links. If you purchase any of the items, I may earn a small commission. It does not change the price of items.

Get paid to take tests. Here is a link to Rare Patient Voice. If you take participate in a study, you can get paid (amount varies). https://rarepatientvoice.com/TheAxialSpondyloarthritisPodcast/

Here are some links to Amazon showing some of the items I discussed.

Ankylosing Spondylitis and Axial Spondyloarthritis The Facts Series by Dr. Khan

Uberlube - https://amzn.to/3i604N2

Here is the Bean Bag neck warmer https://amzn.to/3uN6mcg

Biofreeze - https://amzn.to/33gygBS

Cane - https://amzn.to/3uN9fts

Heating Pad - https://amzn.to/3Bjd5vz

Weighted Blanket - https://amzn.to/36RCdi7

Steff Di Pardo's new book - I Am Not Invisible - https://amzn.to/3JpDScA

All My Ankylosing Spondylitis Shit: Pain and Symptom Tracker by Kinsella Love https://amzn.to/34CHhpx

Show artwork for The Axial Spondyloarthritis Podcast

About the Podcast

The Axial Spondyloarthritis Podcast
A podcast for people with Axial Spondyloarthritis
A podcast for people with Axial Spondyloarthritis. I am Jayson Sacco, a 34 year plus Axial Spondyloarthritis survivor. With this show, I want to bring the AS community together and talk with doctors, organizations, and individuals all dealing with AS.
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