I haven’t been able to get off the floor since it hurts too much to even go around the home, the person said.
Sophie Dillman, a star of Home and Away, has spoken up about her ‘excruciating’ chronic health condition, calling the struggle ”exhausting”.
Utilizing Instagram The actress wrote openly about her struggle with the crippling illness in March 2023.
She shared two photographs that were diametrically opposed to one another and commented, “Endometriosis can look like this or this depending on the day.”
“It hurts too much to even walk around the house this morning, so I haven’t been able to get off the floor.”
But on other days, it has no impact on me at all. Sophie continued, ”I don’t know when the pain, swelling, or nausea will start or end. The unknown is devastating.”
Susan Sarandon, who is also a ”Endo Warrior,” expressed her thoughts on the crippling illness in a quote that Sophie published that same month.
The quote stated, “When all you know is pan, you don’t know that that is not normal.”
In an open interview with 7Life in late 2022, Sophie described the discomfort, symptoms, lack of consciousness, and frequent misdiagnoses of her condition as “frustrating.”
The 30-year-old described endometriosis in her own words, stating that although one in nine people (most often women) may have the ailment, it can range in intensity from being “incredibly painful” to a person “not knowing” they have it.
Speaking of her own experience, Sophie acknowledged that at the age of 21, she had been incredibly fortunate to get a prompt diagnosis.
Many other patients, according to Sophie, endure years of ”perhaps agonising pain, uncertainty, and all kinds of symptoms.
Australian women who are concerned about having the illness must wait an alarming six and a half years on average to receive a diagnosis.
Sophie told 7Life, “I had incredibly painful periods and erratic periods throughout my entire teenage years.”
She continued, ”It was pretty irregular, but when I had them, they were really heavy, really painful,” noting that she would ”faint and vomit repeatedly.
Sophie continued to endure ”amazing bloating,” which was so awful that it made it impossible for her to wear her clothes and caused her to experience ”really bad leg pain and edoema.” But the discomfort and perplexity didn’t end there.
When Sophie decided enough was enough, she went to a doctor and then a gynecologist, who eventually persuaded her to have a laparoscopy, in which a tiny camera is inserted through a tiny incision into the pelvic area to examine and remove any tissue that is causing pain.
After a ”frustrating” wait, Sophie was given her diagnosis following a successful surgery.
It was a relief to know that I wasn’t going insane, Sophie adds.
Sophie has undergone three surgeries, but a cure is still a long way off.
Because it is a part of the lining of many of my organs, Sophie says she has a lot of tissue that doctors are unable to remove.She adds that the operations don’t help her and that it is “exhausting, painful, sometimes awkward, and it stinks.”
Therefore, it appears that I will continue to do it throughout my life.
According to Sophie, the outcomes of surgery were unpredictable because of a lack of research.
Because there hasn’t been enough research done on this subject, she claims that there is no rhyme or reason.
”There are people who have to have surgery many times a year just to cope,” one patient said. ”It’s incredibly irritating again to go back to your doctor and be like, ‘I don’t think this helped.
And when you’re like that, it’s very expensive, very stressful, and very labour-intensive. It’s difficult.
Despite this depressing outcome, Sophie has turned her endometriosis experience into something positive by accepting a position as an ambassador for Endometriosis Australia.
Speaking of the group, Sophie urged anyone receiving an endometriosis diagnosis to connect with others who share their interests and experiences by posting on Facebook and Instagram.
They’re such a wonderful community, she says, and they help you feel less alone.
She continues, “But we need to keep fighting for more funding,” stressing that with more knowledge, diagnoses can be made early and others’ suffering can be alleviated.
You may read more about Endometriosis Australia here.
