Health
MP calls on government to “bold action” to help women living with endometriosis
The government is being called upon to take “bold action” to support 1.5 million women in the UK. Endometriosis..
A report by parliamentarians emphasized the “catastrophic effects” of the condition and found that the diagnosis had not improved in the last decade.
Endometriosis is a tissue -Like the inner wall of the uterus-begins to grow elsewhere in the body.
Charity Endometriosis UK estimates 1 in 10 women in the UK “Endure relentless pain” every day as a result of the condition..
The All-Party Parliamentary Group (AAPG), which surveyed more than 1,000 women, found that even though more than 50% of patients with endometriosis participated in A & E before diagnosis, individuals were still diagnosed with the condition. I found that it takes an average of 8 years.
APPG Chairman David Ames on Endometriosis said the report showed a “lifetime enormous impact” of endometriosis.
“It is unacceptable that endometriosis and its potentially debilitating and damaging symptoms are often ignored or not taken seriously or neglected in relation to the menstrual cycle and duration.” He said.
He emphasized one of the most prominent findings of the investigation. “Only 19% of those who responded to the survey knew that they were found in specialized centers. 90% wanted access to psychological support, but this was not provided. “
The recommendations made to the government are:
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Efforts to reduce average diagnosis time
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Establishing a baseline for diagnosis, treatment and management of endometriosis based on NICE guidelines
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Invest more money in state research
The group also emphasized the need for further study of the experience of patients with endometriosis with LGBTQ +, black, Asian, and ethnic minority backgrounds.
Emma Cox, CEO of Endometriosis in the United Kingdom, said the report “should be a final warning” to the government and NHS agencies.
“The average duration of diagnosis for endometriosis remains eight years. Surprisingly, it hasn’t changed after 10 years. You need to take action to control this,” she said.
“The zip code lottery for access to healthcare professionals specializing in endometriosis must be completed.”
Endometriosis is where the cells and tissues normally found in the endometrium of the uterus begin to grow elsewhere in the body.
These cells behave like cells in the uterus, but unlike menstruation, there is no way to leave the body.
It is estimated that 1 in 10 women has endometriosis. Charity Endometriosis UK refers to people who “endure relentless pain” every day as a result.
It can be debilitating and can have a significant impact in the workplace, and people with this condition need frequent access to the toilet due to symptoms associated with the intestines or bladder.
Symptoms and their effects vary from person to person, but common symptoms include chronic pelvic pain, extreme duration of pain, malaise, bladder and bowel-related problems, organ damage and infertility. I will.
Endometriosis UK says there is currently no cure Because of the symptoms, stressful treatment can “reduce the severity of the symptoms and improve the quality of life” of the patient.
Hormone therapy, which attempts to block or reduce the production of estrogen in the body, can help people in this condition.
Analgesics, including fever, analgesics, physiotherapy, analgesics, and / or the use of TENS machines, are also used as treatment options.
Surgery is also an option for women with endometriosis. Some areas of the affected tissue are surgically removed.
Endometriosis UK Is a charity that helps women suffering from chronic illness.
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