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Q&A with the Mito Community

Q&A with the Mito Community

Q&A with the Mito Community

Grace Robinson

Sep 14, 20215 min read

5 Ways to Celebrate Mitochondrial Disease Awareness Month

5 Ways to Celebrate Mitochondrial Disease Awareness Month

5 Ways to Celebrate Mitochondrial Disease Awareness Month

Grace Robinson

Aug 30, 20213 min read

Healing From Trauma

Healing From Trauma

Healing From Trauma

Grace Robinson

May 29, 20214 min read

America is Failing Disabled Voters

America is Failing Disabled Voters

America is Failing Disabled Voters

Grace Robinson

Oct 18, 20203 min read

Life With Mitochondrial Disease

Life With Mitochondrial Disease

Life With Mitochondrial Disease

Grace Robinson

Sep 7, 20203 min read

Dating While Disabled

Dating While Disabled

Dating While Disabled

Grace Robinson

Aug 1, 20205 min read

Your Wheelchair Fetish Doesn’t Empower Me

Your Wheelchair Fetish Doesn’t Empower Me

Your Wheelchair Fetish Doesn’t Empower Me

Grace Robinson

Jul 21, 20203 min read

Disabled, Dehumanized, and Discriminated Against: Life as A Disabled American

Disabled, Dehumanized, and Discriminated Against: Life as A Disabled American

Disabled, Dehumanized, and Discriminated Against: Life as A Disabled American

Grace Robinson

Jul 16, 20204 min read

Losing A Friend To The Disease You Live With

Losing A Friend To The Disease You Live With

Losing A Friend To The Disease You Live With

Grace Robinson

Jun 30, 20203 min read

I Do Not Care That You Are Being “Forced” To Wear A Mask

I Do Not Care That You Are Being “Forced” To Wear A Mask

I Do Not Care That You Are Being “Forced” To Wear A Mask

Grace Robinson

May 12, 20204 min read

A Weird Time for Everyone: Illness, Isolation, and Hospitalizations

A Weird Time for Everyone: Illness, Isolation, and Hospitalizations

A Weird Time for Everyone: Illness, Isolation, and Hospitalizations

Grace Robinson

May 3, 20204 min read

COVID-19: Thoughts from an Immunocompromised and Medically Fragile Girl

COVID-19: Thoughts from an Immunocompromised and Medically Fragile Girl

COVID-19: Thoughts from an Immunocompromised and Medically Fragile Girl

Grace Robinson

Mar 19, 20203 min read

Why Everyone Should Celebrate Rare Disease Day

Why Everyone Should Celebrate Rare Disease Day

Why Everyone Should Celebrate Rare Disease Day

Grace Robinson

Feb 28, 20204 min read

When the healthcare system forces you to make unfair decisions

When the healthcare system forces you to make unfair decisions

When the healthcare system forces you to make unfair decisions

Grace Robinson

Dec 28, 20195 min read

Winter Bucket List

Winter Bucket List

Winter Bucket List

Grace Robinson

Dec 8, 20192 min read

My First Holiday Without Food

My First Holiday Without Food

My First Holiday Without Food

Grace Robinson

Nov 24, 20192 min read

Becoming Consumed by All Things Medical

Becoming Consumed by All Things Medical

Becoming Consumed by All Things Medical

Grace Robinson

Nov 17, 20192 min read

Finding Joy in Unexpected Places

Finding Joy in Unexpected Places

Finding Joy in Unexpected Places

Grace Robinson

Oct 11, 20192 min read

What is being on TPN really like?

What is being on TPN really like?

What is being on TPN really like?

Grace Robinson

Sep 18, 20193 min read

Mitochondrial Disease Awareness Week

Mitochondrial Disease Awareness Week

Mitochondrial Disease Awareness Week

Grace Robinson

Sep 4, 20192 min read

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Grace & Mito

Grace Robinson

A Life Full of Grace & Mito

Chronic Illness Blogger

graceandmito@gmail.com

Pennsylvania, United States

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