My name is Doris and I am from Kenya, currently studying in the UK.
So in 2003, i started having hard lesions along my elbow and at first I ignored it, but as it progressed along my arm , I decided to seek medical attention, that time the lesions had reached my wrist. it took a few months for it to be diagnosed as Scleroderma. Later in the year, I relocated to Dubai and within a few months all the symptoms cleared a. I relocated back to Kenya 4 years later with no symptoms, as we speak almost all my skin is back to normal.
2 months ago I came to the UK for my Masters after saving for it for a long time. A week after I arrived, I felt the first tingling signs which is usually an antecedent for skin hardening. I assumed that it was because of the cold and so did not think much of it. But over the last week, the signs have increased and I now have the sensations all over my body and I am finding it hard to keep my toes and fingernails warm, the tips of my fingers are drying and scaling.
I am going to see a GP today who will hopefully recommend a specialist. I am sure I will get sufficient advice on how I can manage this but I just wanted to write and tell someone how sad and scared I am feeling at the moment.
I am a single mother to a 10 year old son who is now with my family back home, I quit a job, left my support system, son and everything I know to pursue an education and now I am here cursing myself for not thinking this through, I am thinking I should have put this into consideration.
I am scared as its the beginning of winter (my first winter, ever) and I don't know how much my body will take and whether I will be able to reverse any of this once I go back to Kenya.
Its probably something I am going to be able to manage and I know other people here have it far far worse, but at this minute right now, I cant stop crying and I don't know why.
I am grateful that there is an community that I can talk to.