Aaron Blocker - Invidious

Aaron Blocker

Chronic illness is hard — but you don’t have to face it alone.
I’m Aaron, living with Crohn’s disease and Hypophosphatasia, a rare genetic bone disease. Here, I share the real, raw, and researched side of life with chronic illness — from personal experiences to deep dives into the science behind rare and invisible diseases.

Whether you’re navigating your own diagnosis, supporting someone you love, or simply curious, this channel is your place for honest conversations, education, and community.

Subscribe for:
• Personal stories
• Science made simple
• Rare disease education
• Advocacy and awareness

Let’s build a space of support, visibility, and hope — together.

Connect with me:
Instagram: @aaronblocker_
Facebook: Aaron Block

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19:24

I fought my health insurance and won. | Aaron Blocker

Aaron Blocker

Shared 6 days ago

17 views

7:51

How I Inject my TREMFYA Pen | Aaron Blocker

Aaron Blocker

Shared 1 month ago

301 views

17:10

How to inject using the vial and syringe method! | Aaron Blocker

Aaron Blocker

Shared 2 months ago

181 views

9:37

Patient Advocacy in Action | IBD Social Circle Summit

Aaron Blocker

Shared 4 months ago

37 views

8:48

A life changing diagnosis.

Aaron Blocker

Shared 4 months ago

133 views

14:52

I finished my TREMFYA Loading Dose Infusions! | Crohn’s Disease

Aaron Blocker

Shared 8 months ago

893 views

15:44

My First TREMFYA Infusion! | IBD

Aaron Blocker

Shared 9 months ago

767 views

21:36

What is the CurQD protocol for IBD?

Aaron Blocker

Shared 10 months ago

112 views

18:23

She Made Me an Advocate: Honoring My Mom, One Year Later

Aaron Blocker

Shared 10 months ago

59 views

13:02

Not Science Fiction: A Baby Was Saved by Personalized Gene Editing | Gene Therapy

Aaron Blocker

Shared 10 months ago

55 views

18:09

The End of an Era: Saying Goodbye to Humira After 10 Years | IBD

Aaron Blocker

Shared 11 months ago

1.8K views

11:42

Imagine being really sick and having no answers. | Undiagnosed Day 2025

Aaron Blocker

Shared 1 year ago

78 views

7:14

1 in 10 Americans Live With a Rare Disease

Aaron Blocker

Shared 1 year ago

38 views

19:04

Started my second Humira Biosimilar called Cyltezo

Aaron Blocker

Shared 1 year ago

1.1K views

9:03

Inside My Crohn’s Journey: Colonoscopy & EGD Vlog

Aaron Blocker

Shared 1 year ago

163 views

17:47

Taking My Life Back From Crohn's Disease | AaronBlocker

Aaron Blocker

Shared 1 year ago

126 views

2:01

Five Tips For Living With Inflammatory Bowel Disease (IBD) #IBD #crohnsdisease #uc

Aaron Blocker

Shared 1 year ago

41 views

16:22

Inside the Rare Disease Breakthough Summit: My Journey as a Patient Advocate #rare #science

Aaron Blocker

Shared 1 year ago

28 views

20:34

My Strensiq Journey: Living with Hypophosphatasia | A Treatment Story #rare #strensiq #science

Aaron Blocker

Shared 1 year ago

692 views

1:01

Living with an Ultra Rare Genetic Bone Disease 26th Surgery Recovery #UltraRareDisease #Surgery #HPP

Aaron Blocker

Shared 1 year ago

559 views

25:48

Are you worried about biosimilars? #IBD #biosimilars #crohnsdisease #ulcerativecolitis #science

Aaron Blocker

Shared 1 year ago

108 views

6:58

What is Inflammatory Bowel Disease? #ibd #crohnsdisease #ulcerativecolitis

Aaron Blocker

Shared 1 year ago

42 views

16:51

Finding your chronic illness community.

Aaron Blocker

Shared 1 year ago

24 views

18:49

Vitamin B6 Toxicity and Hypophosphatasia: Are we B6 Toxic?!

Aaron Blocker

Shared 1 year ago

4.1K views

17:28

It’s Rare Disease Day. Here’s why I share my story. #raredisease #hypophosphatasia #rare

Aaron Blocker

Shared 2 years ago

694 views

14:40

Patient Reporter Updates From the Crohn’s & Colitis Congress Conference 2024 #IBD #Crohns #UC

Aaron Blocker

Shared 2 years ago

234 views

22:02

Navigating Career and Chronic illness.

Aaron Blocker

Shared 2 years ago

48 views

15:02

Let’s Talk Surgery.

Aaron Blocker

Shared 2 years ago

66 views

13:30

Today October 30th is World Hypophosphatasia Day!

Aaron Blocker

Shared 2 years ago

51 views

15:08

How to get involved in Policy Advocacy as a Patient.

Aaron Blocker

Shared 2 years ago

17 views

10:08

I was switched to a Humira Biosimilar called Hadlima. #ibd #hadlima #biosimilars

Aaron Blocker

Shared 2 years ago

6.8K views

31:20

My journey to diagnosis of an ultra-rare genetic bone disease called Hypophosphatasia

Aaron Blocker

Shared 2 years ago

256 views

18:36

My Crohn’s Disease Story

Aaron Blocker

Shared 2 years ago

612 views

1:33

Just Because I carry it well doesn’t mean it’s not easy

Aaron Blocker

Shared 2 years ago

47 views

18:49

Who I am and my advocacy

Aaron Blocker

Shared 2 years ago

573 views

1:30

March 22, 2023

Aaron Blocker

Shared 3 years ago

106 views

3:46

Getting diagnosed with a chronic illness. What’s next?

Aaron Blocker

Shared 3 years ago

33 views

1:46

Mini vlog headed to Nashville for treatment of my rare disease.

Aaron Blocker

Shared 3 years ago

26 views