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The condition is getting worse and she fears it will end up killing her.
She said: 'Sometimes I feel like a prisoner in my own home. I have days where I want to crawl into bed and cry but of course, I can't.
'Someone said I could die from it but I don't want to know about my life expectancy. Until they find a cure I just have to live with it. I'm taking each day as it comes.'
Mrs Dell's symptoms began at 16 when she had her tonsils removed. Doctors suspect the pencillin she was given may have disrupted histamine levels in her body.
Her husband, Andy, 32, has given up his job as a delivery driver to be her full-time carer.
She said: 'People didn't understand my condition and would give me a funny look when I told them I couldn't shower.
'My condition is worsening but I don't want to think about what I'll be like in 10 or 15 years.
'Andy has been amazing and does all the things I'm not allowed to do, like the washing up.
'I have to be in and out of the bath in two minutes and Andy has to wash my hair for me.'
There is currently no known cure for aquagenic urticaria but Mrs Dell is trialling a new drug to try to control her condition.
'At the moment I'm taking a drug that transplant patients take,' she said.
'In the same way the drug tells their body not to reject a new liver or kidney, it is telling my body not to reject the water on my skin.
'Next they want to try a drug that cancer patients take to try to build up my immune system.
'The next stage after that is chemotherapy but I don't really want to go down that route because it makes you ill.'
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