<text>  The mother of a two-year-old who is allergic to the sun wants her daughters condition to be recognised as a disability. Monroe Mills has two rare skin conditions, photo-aggravated eczema and solar urticaria, which cause her to break out in painful welts when she spends just seconds in direct sunlight. But it is not just the outside of Monroe that suffers when she is exposed, it is her insides too. Scroll down for video . Monroe Mills has two rare skin conditions, which cause her to break out in painful welts. When she does, the only way to soothe her is to wrap her up in bandages pictured above with her doll also named Monroe Monroe, 2, has suffered from the condition since she was born. She is pictured on the right with her late cat, Marley . Mother Sarah Mills, from Nambucca Heads on New South Wales mid-north coast, told Daily Mail Australia her daughter gets headaches and stomach pains along with becoming lethargic and dizzy. A GP just told us she gets the symptoms outside as well as inside her body, the 28-year-old said. To help prevent this from happening, Monroe wears a head-to-toe bodysuit to cover up as well as slathering on sunscreen and zinc, and wearing a hat and sunglasses. Ms Mills said it was mission for the family to go shopping or to the doctors, and lately the two-year-olds reactions had become so severe that they have had to start carrying around an epipen. Mother Sarah Mills pictured left with her son, Hendrix, and Monroe is fighting to have daughters conditions recognised as a disability . Exposure to the sun causes painful welts and means Monroe spends most of the night awake. Ms Mills said she averages four hours sleep on a good night The flare-ups could also be caused by fluoroscent lights inside shopping centres . She said Monroes flare-ups could happen any time her daughter stepped into the sunlight. She could be outside for 20 seconds or just a matter of minutes before she would break out. We just remain as indoors as much as humanly possibly, Mr Monroe said. We run into the shops as fast as we can from the car. If we wanted to go shopping, shed have a flare up from the fluorescent lights. When Monroes skin does break out in welts, the only way to soothe her is to put her in a bleach bath, apply steroid creams, and then wrap her in wet and dry layers of bandages. This happens so often now that the little girl becomes distraught when she sees her mother getting out any type of cream. Shes become extremely scared of creams. When she sees the sunscreen or steroid creams come out she starts crying, Ms Mills told Daily Mail Australia. Shes had enough of being creamed up 24 hours a day. At night, she breaks down and starts crying because shes so itchy and in pain. The two-year-olds brother, Hendrix pictured on the left, has autism. Ms Mills recently had to quit her job to become Monroes full-time carer . To prevent her breaking out, Monroe dons a head-to-toe bodysuit pictured along with slathering on sunscreen and wearing sunglasses . This is Monroes every day life and her welts can last for 20 minutes to several hours. Broken sleep patterns are the norm for her and Ms Mills who averages about four hours a night on a good night. Its extremely heart breaking to watch her in so much pain. Now that she is at the age where she can put two and two together she asks from the back seat while were driving to doctors: Why does the sun hate me, Mummy?, Ms Mills said. It just shatters my heart for her when she thinks that the sun hates her. Its really confronting. On top of looking after Monroe, Ms Mills also has an autistic five-year-old son, Hendrix. She recently had to quit her job to become a full-time carer. People point and laugh at Monroe left when she is in her bodysuit right and Ms Mills wants that to stop by raising awareness of her daughters conditions . The single mother-of-two has started up a fundraising campaign to help her cover the costs of caring for Monroe, which include a special 50 sunscreen and 200 in fuel costs a month to visit a doctor in Newcastle. Ms Mills said she spends at least 200 a week on meeting Monroes needs alone. She gets no other assistance from the Federal Government other than a carers allowance because they do not recognise Monroes conditions as a disability. I cant work because of how demanding her needs are. No employer is going to be okay with me taking every second week off because Monroe is in hospital, she said. Ms Mills says she has reached breaking point while caring for Monroe and is trying to get more help . At first, Ms Mills used her Miracle for Monroe Facebook page to raise awareness of her daughters conditions because people were laughing and pointing at her in the street when she wore her bodysuit. In the beginning, she was pointed at and laughed at, not just by kids but adults too. She picks up on it now and I want everyone in the world to know about her conditions and stop laughing at her, Ms Mills said. I want people to understand the struggles shes going through. We have people ask her whats wrong with her and I tell them shes allergic to the sun and people say: Thank goodness, I thought she had been burnt. Im not saying being burnt is not bad, but theres a light at the end of the tunnel. Whereas Monroe is in constant pain and doctors are happy to say stay home. She cant even play in the park. What kind of life is that? To donate to Monroes cause, visit her gofundme page. 