Hi.

I'm Jaimar Tuarez.

My life changed when my doctor told me ‘’You have Multiple Sclerosis.’’ 

And here began my autoimmune journey. 

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Hope is the only thing stronger than fear.
Suzanne Collins

Jaimar in Venezuela .....

About Me

More About Me....

Hello! I’m Jaimar, but you can call me Jai. I’m 22 years old. I was an average university student in Venezuela: I studied, worked, helped my family… Until December 2023 when my life would change completely: 

I was diagnosed with Multiple Sclerosis.

 

My Goals

Life in Venzuela

Venezuela is in crisis, everybody knows that. Since 2015, Multiple Sclerosis patients have been in absolute neglect: there is no medication.  No comprehensive care, no options for nearly 10 years. 

Medications for Multiple Sclerosis are among the most expensive in the world. In Venezuela, prices range from $12,000 to $30,000 annually, in a country where 94.5% of the population is in poverty. How is it possible to access healthcare under these conditions? 

The AFP released a report in February 2024 about the situation of MS patients in Venezuela. You can read it here:

https://www.rfi.fr/en/international-news/20240224-emigrate-or-waste-away-dilemma-for-venezuela-multiple-sclerosis-patients

In my case, there is one viable option and that is to emigrate to a country where I can get treatment and begin to heal while starting a new life. Below are two ways you help me reach my goal.

I currently have two campaigns, one for treatment and one for emigrating. I would be very grateful if you could spread the word. Thanks to everyone who can contribute in any way. 

Emigration

To help Jaimar emigrate away from Venezuela where she can get the healthcare she needs please visit the following go fund me link:

Infusion Treatment

To help Jaimar get the treatment she needs immediately to fight multiple sclerosis, please visit the go fund me link below.

My Blog

Follow My Journey

Fase 1: La negación El
duelo,
del
latín
dolus:
dolor. El concepto del duelo ha evolucionado. Anteriormente, se consideraba que era únicamente ante la pérdida -física- de una persona. No …

Viviendo con EM: El diagnóstico
Parece que el guionista de vida le gusta la comedia. ...