rare diseases • Chronic Illness Blog: Life with CVID

Common Variable Immunodeficiency

SCIg Series: Navigating anxiety about infusions

May 13, 2023 / 1 Comment

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Aubrey

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“I am Immunocompromised” Card for Doctor’s Visits
August 6, 2022

Reflecting on four years with Common Variable Immunodeficiency (CVID)
August 23, 2023

Are Plasma Treatments Painful?
October 27, 2022
Chronic Illness

Dating with a chronic illness: How and when do I tell someone about my disease?

May 2, 2023 / 5 Comments

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Aubrey

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Suffering from constant sinus infections? Here are 2 things that help alleviate my sinusitis symptoms.
May 4, 2023

3 Supplements That I Love!
May 27, 2023

The importance of community for those with chronic illness
December 19, 2023
Common Variable Immunodeficiency

Saving Lives: Why it’s important to donate plasma

April 26, 2023 / 6 Comments

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Aubrey

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Reflecting on four years with Common Variable Immunodeficiency (CVID)
August 23, 2023

Living with CVID: How chronic illness changed my outlook on life.
April 11, 2023

International Plasma Awareness Week 2024: The importance of raising awareness for plasma donation
October 7, 2024
Common Variable Immunodeficiency

National Primary Immunodeficiency Month: 3 Ways to Celebrate Your Strength

April 25, 2023 / 2 Comments

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Aubrey

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Guest Post: Maia’s CVID Story
March 12, 2025

World PI Week 2024: Spreading Awareness For Primary Immunodeficiency
April 17, 2024

What is immunoglobulin replacement therapy (Ig)?: My experience with starting Ig
November 6, 2023
Common Variable Immunodeficiency

Living with CVID: How chronic illness changed my outlook on life.

April 11, 2023 / 8 Comments

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Aubrey

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SCIg Series: sometimes I really don’t want to do it.
March 31, 2023

Are Plasma Treatments Painful?
October 27, 2022

Guest Post: Kendal Phinney’s CVID Story
January 25, 2024
Common Variable Immunodeficiency

SCIg Series: sometimes I really don’t want to do it.

March 31, 2023 / 7 Comments

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Aubrey

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Recently diagnosed with Common Variable Immunodeficiency (CVID)? Here’s my advice for the beginning of the journey
May 30, 2023

IDF’s Walk for Primary Immunodeficiency – how to get involved!
September 11, 2023

International Plasma Awareness Week 2024: The importance of raising awareness for plasma donation
October 7, 2024
Chronic Illness

Life with an Invisible Illness: Why do I feel so guilty about taking time for myself?

March 28, 2023 / 8 Comments

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Aubrey

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The importance of hydration for those with chronic illness (and everyone!)
July 11, 2023

Swollen Lymph Nodes – cancer, or something else??
August 17, 2022

When Chronic Illness is a Full Time Job
November 30, 2022
Chronic Illness

What is Primary Immunodeficiency? 3 things I’ve learned about PI

March 24, 2023 / 0 Comments

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Aubrey

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Listen to my guest feature: Real Talk Real Women by Gemma Serenity Gorokhoff
June 20, 2023

When you’re sick and tired of being sick and tired
August 28, 2023

Swollen Lymph Nodes – cancer, or something else??
August 17, 2022
Common Variable Immunodeficiency

CVID Symptoms: How do I live a “normal” life?

March 21, 2023 / 1 Comment

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Aubrey

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Guest Post: Maia’s CVID Story
March 12, 2025

Reflecting on four years with Common Variable Immunodeficiency (CVID)
August 23, 2023

National Primary Immunodeficiency Month: 3 Ways to Celebrate Your Strength
April 25, 2023
Chronic Illness

Rare Disease Day 2023: raising awareness for over 6,000 rare diseases

March 1, 2023 / 5 Comments

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Aubrey

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What is Primary Immunodeficiency? 3 things I’ve learned about PI
March 24, 2023

Telling your chronic illness story: An intimidating yet rewarding experience
March 15, 2024

Living, Healing, and Hitting Pause: Navigating the quiet demands of life with chronic illness
March 11, 2026