Her Campus Logo Her Campus Logo
Sunset Ocean Beach Sky Evening
Sunset Ocean Beach Sky Evening
Charlotte Reader / Her Campus
Life

Living with a Rare Condition

This article is written by a student writer from the Her Campus at Manhattan chapter.

This past week, I went to the doctors and found out that I’m allergic to shellfish. The reason that an allergy test was conducted for me is because I’d been having a lot of stomach problems lately, including a trip to the emergency room in January because of it. But I’ve been having stomach aches, weight loss and other on and off problems like this since I was little. When I was 15, I was formally diagnosed with ulcerative colitis, a not so common digestive/stomach problem. I tried multiple things and many doctors, but it never truly went away. It wasn’t until this week, that they finally even attempted to find out what could be a big factor in contributing to my ulcerative colitis.    

If you know me, or if you’ve been following my blog for awhile, you will know that I also suffer from a rare condition called Vulvodynia. For those who don’t know, or for a refresher, Vulvodynia is when one has an abnormally tight vaginal area, and can make inserting anything in there painful.  It makes it very difficult, and sometimes impossible for someone with this condition to have sex, get pap smears or even do something as simple as put a tampon in. Again, it’s rare, and doctors don’t have a lot of research or answers for it. 

What do both my stomach problem and Vulvodynia have in common? They’re both rare medical disorders, and I have to live with them. They’re obviously not life threatening like cancer or something more severe, but they contribute to my quality of life. I’m not going to sugarcoat it, they both suck. Having a rare medical condition means that not a lot of research is done on your issue, and I think that’s something that’s very frustrating. You want answers. You want solutions. But you almost never get them. It feels like doctors just give up on you, and that really sucks. Even though sometimes it isn’t their fault, it often feels like I am not treated like a priority just because they “can’t do anything right now” or it’s “complicated and really difficult to treat.”

Having a rare condition also means you feel really alone sometimes because not many people understand what you’re going through; it really makes you feel like you don’t have anybody to talk to about it. Then there will also be the people that think you’re imagining things. “It’s just stress,” they’ll say, even though you’ve been suffering for years and you know for a fact it’s definitely not that. 

This may not be the most uplifting article in the middle of all that we’re going through, but I just felt it had to be said for the people that go through something similar. Though you may feel alone, you never truly are. You will get through it somehow.

 

Molly Prior

Manhattan '21

Molly Prior is a senior at Manhattan College studying communications and journalism. With a passion for women's empowerment and lifestyle, she hopes to write for a magazine such as Cosmopolitan or Women's Health.
As an avid lover of all things writing related, Christine is a born story-teller. She is a junior at Manhattan College majoring Public Relations and minoring in Marketing. When she’s not writing, you can find her exploring NYC, binge watching The Office, or enjoying a good cup of tea. She joined Her Campus after transferring to MC and absolutely fell in love with it! She is currently the Campus Correspondent of her chapter, and hopes her articles can entertain and inspire women everywhere. After college, she plans to continue writing and hopes to publish a book one day. Be sure to check out her college lifestyle blog Christineeve.com!