After years of being embarrassed by the symptoms, they were able to diagnose their illness and change their lives

How many times does it happen to us that we don’t tell anyone if there is any symptoms that embarrass us? And so much so, that we no longer went to the doctor to see what could be the pain of it.

This is what happened to a young woman 21 years who was diagnosed with a chronic illness after many years of dealing with the disease without talking about it to his closest people.

Megan’s story

Megan McNeilwho is 21 years old and lives in Lisburn, Ireland, has lived with symptoms for more than four years: losing blood when going to the bathroom. And, because of the nature of this problem, he didn’t even dare tell his family.

However, before a trip, they discovered clues in the bathroom and he had to tell them about it. “When I was 17, I went to New York and my mother saw blood in the bathroomso I have to tell him what’s going on, ”he said Belfast Live.

At that moment he had already begun find a solution and now he recounted how the path to discovering what he had and how he could solve it.

Concerning what he did he said: “My mother got me doctor’s appointment bedside for our return and they sent me for an endoscopic test, ”he said.

He added: “I was first diagnosed with proctitis with only a few centimeters of inflammation in the intestine and they sent me home with anti-inflammatory medication“.

But his problem persisted. Over the next three months she got worse and worse, bleeding uncontrollably and sometimes going to the bathroom 15 or 20 times per hour. Hell is his life.

“I’m tired of being wake up in the bathroom all night, there are times I don’t even go out of the bathroom, sometimes it breaks my soul. I am many fatigue and I slept where I could, my mouth full ulcers and there was a constant pain“.

In addition, Megan suffered a severe weight lossSo he went back to the doctor.

“I am skin and bonesHe looked at me and said I was leaving emergencies Immediately, they took me directly and I started on an intravenous line, but it kept getting worse, ”he said in a media dialogue.

At first, professionals thought it was up to them appendix, so they took him to a hospital for surgery. “When I arrived, they quickly realized that I was not in the emergency room weakening with painMy blood pressure is going down and I can’t go to the bathroom anymore. “

The solution finally came

Fortunately, the next day he was diagnosed ulcerative colitis and began taking a biologic IV that he would need every 6 to 8 weeks along with high doses of steroids.

“This whole process took four months to be tested from the first date, it is faster than in other cases, but I went to the hospital for a month as they tried to control my symptoms.“, he describes.

For the next year, Megan was in and out of the hospital every few months with a severe flare -up of her condition. He is still subject emergency surgery in which he came out carrying a colostomy bag and a big shock.

“I would have died if I hadn’t had surgery and my doctor told me I would probably have to have more surgeries in the next five years,” he said.

That way, they give him a chance rebuild your body and allow have childrensomething that the next surgery will reduce and her chance of getting pregnant and getting pregnant will be 50%.

“People think that this disease only affects their intestines, but it’s more than that”the young woman admitted while making sure it was a mental challenge to come out of an important operation with something that changed her life.

Now, after the obstacles she has faced and continues to face, the young woman stands up for others who may find themselves in similar situations. recounting his experience in networks. In addition, it has modeling for well -known brands.

“My body has taken so much away from me and betrayed me for so many years that now I am ready to take it back and show exactly what I and thousands of others are going through.”