Help with a Legal Precedent Case for CFS/ME

The Issue

There are over 2 MILLION people in the U.S. alone, most of whom are women, that suffer from most horrible, debilitating, completely misunderstood, and often dismissed illness called Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (ME). 

https://www.medscape.com/viewarticle/908622?src=par_cdc_stm_mscpedt&faf=1

To make things worse, many CFS/ME patients are labeled as mentally ill, as lazy, as making things up (hypochondriacs), or with other diagnoses that result in severe progression of CFS/ME.

https://www.cdc.gov/me-cfs/patient-stories/index.html

CFS/ME patients are often neglected, abused, mistreated by their families, friends, and especially medical professionals, which only adds to the peril and suffering that they go through. Some CFS/ME patients even paid with their lives as a result of everything stated above.

http://www.shoutoutaboutme.com/about-me/severity/body-count-the-tragic-stories-of-severe-me/

Therefore, we, CFS/ME patients of the U.S. and the world are begging all and any legal firms/legal professionals to help us set a precedent case, here in the U.S., for brazen medical malpractice that most of us experience for decades on a daily basis, which results in us not being able to get any medical help we desperately need, nor to get proper treatment and care for our horrible illness.

In particular, we are sincerely and wholeheartedly asking The Cochran Law firm to take and win the psychiatric malpractice case of Aleksandr Sigalov so that the precedent is set for all other CFS/ME patients, and so that Aleksandr can get justice and medical treatment/care that he was completely deprived of for almost two decades.

If Cochran firm or any other law firm will help Aleksandr and us to win, you will be heroes and saviors of most abused, neglected, and suffering people who need help, support and understanding from everyone.

 

Sincerely yours,

 

Millions of CFS/ME sufferers worldwide.

 

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A SPetition Starter

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The Issue

There are over 2 MILLION people in the U.S. alone, most of whom are women, that suffer from most horrible, debilitating, completely misunderstood, and often dismissed illness called Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (ME). 

https://www.medscape.com/viewarticle/908622?src=par_cdc_stm_mscpedt&faf=1

To make things worse, many CFS/ME patients are labeled as mentally ill, as lazy, as making things up (hypochondriacs), or with other diagnoses that result in severe progression of CFS/ME.

https://www.cdc.gov/me-cfs/patient-stories/index.html

CFS/ME patients are often neglected, abused, mistreated by their families, friends, and especially medical professionals, which only adds to the peril and suffering that they go through. Some CFS/ME patients even paid with their lives as a result of everything stated above.

http://www.shoutoutaboutme.com/about-me/severity/body-count-the-tragic-stories-of-severe-me/

Therefore, we, CFS/ME patients of the U.S. and the world are begging all and any legal firms/legal professionals to help us set a precedent case, here in the U.S., for brazen medical malpractice that most of us experience for decades on a daily basis, which results in us not being able to get any medical help we desperately need, nor to get proper treatment and care for our horrible illness.

In particular, we are sincerely and wholeheartedly asking The Cochran Law firm to take and win the psychiatric malpractice case of Aleksandr Sigalov so that the precedent is set for all other CFS/ME patients, and so that Aleksandr can get justice and medical treatment/care that he was completely deprived of for almost two decades.

If Cochran firm or any other law firm will help Aleksandr and us to win, you will be heroes and saviors of most abused, neglected, and suffering people who need help, support and understanding from everyone.

 

Sincerely yours,

 

Millions of CFS/ME sufferers worldwide.

 

avatar of the starter
A SPetition Starter

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Cochran Law Firm
Cochran Law Firm
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Medical Malpractice Lawyers
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Petition created on May 28, 2019