
By Alyce Collins
THIS WOMAN was treated like a leper by stumped doctors and colleagues until a dermatologist eventually diagnosed her with a severe case of psoriasis.
Retail manager, Marina Tirabassi (23) from Ontario, Canada, found herself overloaded with work as well as studying when she started noticing patches of psoriasis on her body because of the stress.

Marina Tirabassi / MDWfeatures
However, when her psoriasis spread all over her body, the diagnosis she received from the doctors wasnāt what she anticipated when they told her it was Scarlet Fever and made her wear a mask in case she was contagious.
Marinaās psoriasis started on her chest, but it soon began developing on her face and stomach. At first, she tried not to worry about the small patches because she was aware that stress could affect her skin, but once it was covering her body she sought a medical diagnosis.

Marina Tirabassi / MDWfeatures
The first doctor Marina saw diagnosed her skin condition as Scarlet Fever and gave her antibiotics, but after two weeks of no change, Marina began doubting this diagnosis. The second time round, Marina had blood tests taken and was tested for measles and mumps, but every test came back negative.
After a month of getting no answers, Marina searched for a dermatologist who finally gave her the diagnosis of Guttate Psoriasis, an autoimmune disease which can cause spots of itchy, red skin all over.

Marina Tirabassi / MDWfeatures
āIn April 2017 I took a promotion at work and I was taking on more hours than I was used to, and I had a lot of responsibilities,ā said Marina.
āNormally I wouldnāt have had any issues with that, but it all happened right in the middle of my final exams, so I wasnāt sleeping or eating properly. I then came down with strep throat as my body was so weak.

Marina Tirabassi / MDWfeatures
āThe first patch I noticed was on my chest, but I only began to really notice it after it developed on my face. It wasnāt until it appeared on my stomach that I became concerned.
āWhen I was first diagnosed with Scarlet Fever I knew it was weird, but the rash looked very similar to the symptoms, so I trusted my doctor and didnāt think much of it.

Marina Tirabassi / MDWfeatures
āI continued taking the antibiotics that he prescribed, and it wasnāt until two weeks later when it still wasnāt going away that I started to doubt the diagnosis.
āI took a trip to the hospital because Iād never seen anything like it. The doctors ran a whole bunch of blood tests and they were all stumped, so they just gave me Benadryl and sent me on my way.

Marina Tirabassi / MDWfeatures
āI felt completely defeated. I sat in the hospital for eight hours while they continued to poke at me and take my blood.
āEven the woman in triage forced me to wear a mask and everyone treated me like I was contagious. I didnāt even take the Benadryl because I knew it wasnāt an allergy.
āAfter a month of not knowing what was wrong, I finally went to see a dermatologist who eventually diagnosed me with Guttate Psoriasis.ā

Marina Tirabassi / MDWfeatures
Guttate psoriasis can be triggered by bacterial infections as well as stress, and it causes red droplet-size marks on the skin. For some, this type of psoriasis will disappear within a matter of weeks, but cases like Marinaās can take longer.
When Marina was finally told correctly what her condition was, she was able to change a few factors in her lifestyle in the hopes of improving her psoriasis.
āThe dermatologist knew what was wrong with me as soon as she looked at my skin and asked about the symptoms,ā said Marina.

Marina Tirabassi / MDWfeatures
āAs soon as she knew I had strep throat right before it happened, combined with an intense amount of stress, she knew. She didnāt even have to do the skin biopsy.
āIn that moment I had so many mixed emotions. I felt incredibly relieved and happy that someone could finally tell me what was going on.
āI was happy that I would finally be able to start an appropriate treatment that would actually help me. But I did feel incredibly low because I didnāt know much about auto-immune diseases at that time.
āHearing the word āincurableā made me feel defeated. I didnāt feel like the treatment would work and I believed my skin would look this horrible and be this painful for the rest of my life.

Marina Tirabassi / MDWfeatures
āI scratched my skin far too often. Itās so incredibly dry and itchy, so itās very difficult to resist itching it. I kept trying to remind myself that if I scratched it I would leave my skin scarred.
āWhen I went out in public I couldnāt handle the looks from most people. I had people at work ask if I was contagious and I began to feel ashamed of showing my skin.
āI covered up as much as possible to avoid this. I also started doing a lot of research into psoriasis and natural diets to help flare-ups.
āI tried to stay away from junk food and foods which are high in saturated fats and refined sugar which can promote inflammation. I also stopped drinking because alcohol is really bad for flare-ups.ā

Marina Tirabassi / MDWfeatures
Another factor which has helped towards Marinaās skin clearing up is UVB phototherapy treatment which had an instant effect.
āPhototherapy involves exposing the skin to ultraviolet light on a regular basis under medical supervision,ā Marina added.
āI had to drive an hour and a half away to Toronto three times a week to do the therapy. UVB slows the growth of affected skin cells.
āThe results from this were pretty much immediate. I noticed changed after the first three sessions of UVB. It started to reduce the redness immediately and I was left with just light spots on my skin which eventually cleared away.

Marina Tirabassi / MDWfeatures
āI feel very proud of myself. Right now, my skin is completely clear, and itās made me feel super confident.
āAlthough I do still have moments where I feel depressed and scared that it will return at any moment, I do my best to remain positive and to use my experience to spread awareness about autoimmune diseases.
āI feel like a warrior, and I may be fearful that it could return, but I know I can handle it.
āI havenāt experienced a big flare-up since completing the treatment. I still get small patches here and there, but nothing thatās really itchy or uncomfortable.
āThe biggest challenge I had during that time was having to answer, āare you contagious?ā. The biggest thing that contributed to feeling so low was the looks of disgust that people gave me for something over which I had no control.
āIt was difficult, but I began to realise that I canāt blame people for looking at me like that because theyāre not educated about my condition.

Marina Tirabassi / MDWfeatures
āCovering up my experience wonāt help spread awareness about autoimmune diseases. We live in a society that is so corrupted by what we see in the media so when we see someone who looks different, we automatically assume itās abnormal.
āI decided to embrace my psoriasis, so I could help people understand and help others who are going through something similar.
āTreating my condition has allowed me to feel comfortable in my own skin. Before this, I had such an altered idea of what it means to be beautiful. Living with psoriasis has taught me patience because it takes time to heal.ā
To find out more, visit Marinaās Instagram, @psoriasis_warrior66