Endometriosis: disability arrives with this procedure revealed by the lawyer

Endometriosis, a disease that afflicts thousands of women. How does the state protect these people economically?

Endometriosis, an often unrecognized chronic disease, continues to be a challenge for millions of women around the world. Characterized by the presence of endometrial-like tissue outside the uterus, this condition can cause debilitating symptoms and significantly affect the quality of life of affected women. Now, fortunately, it arrives to mitigate the suffering a form of economic welfare.

One of the main challenges associated with endometriosis is its silent nature and difficulty in diagnosis. Many women with this disease can spend years before receiving an accurate diagnosis. Years of dealing with painful and disabling symptoms without a clear explanation. This delay in diagnosis can have a significant impact on patients’ physical and mental health, affecting their work, relationships and overall health.

Symptoms of endometriosis vary from woman to woman. They can include intense pelvic pain during your menstrual cycle, pain during sexual intercourse, abnormal bleeding, chronic fatigue, and digestive problems. These symptoms can have a devastating impact on women’s daily lives, limiting their ability to work, participate in social activities and pursue their life goals.

Currently, There is no definitive cure for endometriosis, but there are treatment options available to manage symptoms and improve patients’ quality of life. These include medications to relieve pain, hormone therapies to reduce the growth of endometriotic tissue, surgeries to remove deposits of abnormal tissue, and complementary therapies such as physical therapy and stress management.

Endometriosis: the procedure for obtaining disability

Raising awareness about endometriosis is essential to improve early diagnosis, ensure timely access to treatments and reduce stigma associated with the disease. Women with endometriosis need support from their healthcare providers, their families and society as a whole.

Cinzia Laurenza, a lawyer expert in patient rights, in an interview published on the Sky Tg 24 website, takes stock of the protections and benefits for women who live with this chronic and disabling disease. The path to recognizing the rights of women affected by this disease is still long and tortuous. The Italian Parliament began to take an interest in endometriosis only in 2006, but despite several legislative attempts, little has been done to guarantee adequate protection. Only recently has endometriosis been included in the ministerial evaluation table of disabling pathologies, allowing patients to obtain medical certification more easily.

The evaluation of endometriosis in terms of civil disability is a complex process that depends on the severity of the disease and its effects on work and daily activities. However, despite progress in including endometriosis in the Essential Levels of Care (LEA), many women still find themselves struggling to obtain adequate recognition of their rights. Currently, Severe endometriosis can only be recognized with a maximum of 25% civil disability. A percentage that many believe is insufficient to reflect the real impact of the disease on patients’ lives.

Despite the challenges, there are paths that women with endometriosis can follow to have any hope of having their rights recognized. It is essential that patients inform themselves about their rights and the civil disability assessment processes, and that they contact qualified professionals for legal and medical assistance.