Health

Read this if you’re asking, “Is Endometriosis a Disability?”

Read this if you're asking, "Is Endometriosis a Disability?"
Written by adrina

Endometriosis is a chronic condition that can have a significant impact on daily life and activities. But it’s not considered a disability by most medical professionals or the law.

That’s likely because long-term conditions like endometriosis can have variable effects, with some people having more severe symptoms and others being able to manage their symptoms without specialist care and treatment.

Although endometriosis is not officially recognized as a disability, many people who live with it and know how disabling it can be use the term.

It’s also possible that disability benefits are available if you find that the condition is severely limiting your ability to lead a normal life, especially where work is concerned.

Because endometriosis causes tissue similar to the lining of the uterus to grow elsewhere in the body, it can be accompanied by a wide range of symptoms.

This can include:

Some people may not have noticeable symptoms or may be able to manage them to the point where they can participate in everyday activities.

But others have debilitating symptoms that affect their ability to do everyday things.

Until now, not a strong connection was found between the severity of endometriosis tissue growth and the severity of symptoms. So some people with more severe endometriosis may experience less pain than people with milder forms.

Pain can be one of the hardest things to deal with — so much so that endometriosis has been linked to a bigger chance the development of anxiety and depression and the potential for the body to become particularly sensitive to pain over time.

Endometriosis is currently not curable. However, there are several treatments that should be considered to manage and relieve symptoms such as pain. They mainly include medication and surgery.

Because endometriotic tissue grows in response to hormonal stimulation, medications that lower hormone levels can be used to limit the growth of endometriotic tissue.

Medications that can help with endometriosis symptoms include hormonal birth control such as oral contraceptives and gonadotropin-releasing hormone (GnRH) agonists, which work by causing a temporary state of menopause.

Medical treatments can come along side effects such as insomnia, headaches and hot flashes. And the symptoms of endometriosis may flare up again after stopping such treatment.

Surgery to remove tissue may be useful for more severe symptoms or when hormonal medications are not helping.

Sometimes hormonal medications can be re-administered after surgery. Again, it is possible for tissue to grow back after surgical removal.

Other treatment options include pain relievers, complementary therapies such as acupuncture, and dietary supplements.

A final option is a total hysterectomy. This is usually not considered until several other treatments have been tried.

For those with endometriosis who are actively trying to conceive, most of these treatments, such as birth control pills or a hysterectomy, are not viable options.

Endometriosis can affect your fertility in a number of ways, which can make it harder for you to conceive. Talk to a doctor or fertility specialist about your symptoms. They may be able to recommend more advanced fertility treatments to support the pregnancy.

“For many, endometriosis is not only difficult to diagnose medically,” says Kryss Shane, LSW, LMSW, “but typically results in loved ones being told at length that period pain or abdominal pain is ‘a woman’s bane’ or ‘all on your mind ‘ or similar.”

Over time, this – along with the feeling of being dismissed from medical professionals –“Can demoralize the person and cause them to start questioning themselves,” Shane continues. “For those who don’t identify as women, this can also reinforce gender dysphoria.”

The chronic pain and other symptoms that can accompany endometriosis can also severely interfere with everyday life.

It can limit a person’s ability to leave home and participate in social or professional activities, potentially making it difficult to achieve certain life goals.

Lack of energy can also make basic household chores difficult. Feelings of guilt or frustration can then arise.

Also, endometriosis usually occurs at times when there are significant changes in a person’s life, such as B. during puberty, which in turn complicates these social, relationship and career transitions.

Of course, people with milder or no symptoms are much less likely to experience such effects on daily life.

People tend to form important social networks during puberty. Experiencing endometriosis symptoms during this time can negatively impact one’s ability to form such relationships and engage in early social life.

This can continue to affect people as they age. in the an endometriosis studyAmong the most notable effects was the impact on social life across all age groups.

People reported staying at home and missing out on social activities or giving up enjoyable hobbies like sports.

They also mentioned distancing themselves from others due to feelings of jealousy or experiencing conflicts with others due to symptoms such as pain and mood swings, which naturally led to feelings of isolation.

The fact that other people can’t see endometriosis can make it all the more difficult when it comes to relationships with friends and family.

Intimate relationships can also feel the effects.

Pain during or after penetrative sex can lead people to avoid or interrupt sexual activity. This can be emotionally difficult for both people with endometriosis and their partners. But partners can be an important source of support during flare-ups and awaiting treatment.

Possible effects on fertility are also of concern. Some people worry about finding a partner who is willing to accept possible infertility while others are already in relationships reported negative effects.

Chronic pain can lead to dropping out of school or college.

in the researchPeople have mentioned missing out on educational opportunities or don’t track Continuing education due to endometriosis symptoms.

The feeling of not being able to reach a higher level of education can also affect career opportunities.

in the a survey Of 107 women with endometriosis, 40% believed that their career development was directly influenced by endometriosis. As examples, they cited missing out on bonuses and promotions and losing customers.

However, it should be noted that the participants were classified as having severe symptoms, so not everyone with endometriosis will experience the same.

General working life can also be disrupted. Some must and can be taking days off or longer absences less productive total.

All of this can lead to a complete career change for some people opt for less stressful jobs or part-time jobs.

Endometriosis can make you feel isolated. But there are many people to talk to who are in the same position and experts who can help.

The following websites and organizations offer resources to learn more about the condition, help manage symptoms, and connect with others who understand how you’re feeling:

You can also find many endometriosis support groups on social media.

For more information and advice on applying for disability benefits, visit the Social Security Administration (SSA) website.

Endometriosis can come with a wide range of symptoms, and they can be mild, moderate, or severe.

While some people find the condition disabling and less able to function socially or professionally, others may have milder symptoms that are more easily managed.

Early diagnosis and effective treatment are critical to reducing the negative impact of endometriosis on everyday life.

So use the resources above to try to build a support network and find a team of specialists who will listen, understand and take action.


Lauren Sharkey is a UK-based journalist and writer specializing in women’s issues. When she’s not trying to find a way to banish migraines, she can be found uncovering the answers to your lurking health questions. She has also written a book introducing young activists around the world and is currently building a community of such resisters. start her Twitter.


#Read #youre #Endometriosis #Disability

 







About the author

adrina

Leave a Comment