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Psoriasis (plague) sufferer Feb (Pics from The Sun) and Now..( July 6th/Pool shoot) taken in Fuerteventura, Canary Islands, Spain.
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| February Shoot for The Sun after my Dad passed away/relationship breakdown caused this.. |
July 6th 2016
I still suffer with the condition.(Trunk/Bottom/Inside thighs/pelvis. I have had light treatment 7 weeks of at Basildon University Hospital . My local surgery (Thorndike) I have made a full complaint to the surgery (june 2016)and Medway Hospital (Dermatology) as they STILL wont see me and it is VERY bad in the areas mentioned.
I also wrote to my local MP at the negligence and being put in a queue still when this is coming back yet again after more than a year of waiting and waiting some more... I now am to be put on immune suppresant drugs, which thus needs a few injections including flu injection before I am to take this new medication. I was told I cannot have the injection until next year by Thorndike Surgery, Rochester, Kent! So again after losing letters/messing up my medication so badly needed, and now telling me I cannot have injection I desperately need so badly to stay well and clear!
The likes of Josie Cunningham gets a breast enlargement at the tune of £4,500 for having nothing wrong with her, apart from a flat chest in life! Its such an injustice!
After them not letting me see a Doctor and only the nurse because it was 'only' psoriasis. I lied in the end and told them I HAD to see a Doctor NOT the nurse for 'Ulcerative Colitis', another permanent medical condition I suffer with. Finally on seeing the Doctor who was terribly shocked at how my immune system is attacking itself told me Medway Hosp had 18wk plus wait! This was Feb this year. I was in turmoil and depressed and in terrible pain with skin falling off and bleeding. And then it started attacking my scalp. My hair is very thin now and hasnt grown back.. Basildon Hospital is an hour away from Rochester, Kent where I live and was 30 day wait.
After being ill for so long .. This condition started around December 2014 and spread at a rapid rate. The creams have not worked, though they do hydrate.
I cannot tell how nice it is to even get into a bikini after looking the way i did when illness/condition was at its height in February 2016. As a woman, one who likes to dress feminine it became impossible. Even to wear a dress with legs, arms or my breasts out was completely out of the question.
This has been a difficult soul destroying time stripping me of my feminity and everything else. My message is DONT ignore a few patches of scaly itchy skin. Go to the Doctor. The fight isn't over and I am far from clear! I really feel if you are ill with a skin condition it should be by the severity, it should be judged. And not by what number you are in the system. I saw dermatology a local office and the referral was still sent as 'not urgent'.. I thank Basildon Hospital and especially Dr.Anika Khan (dermatology). If it wasn't for her I would have taken my life in the end because of how it had taken over my life and my own local surgery and hospital would not listen or help until I complained in the highest possible way. I have a letter from the houses of parliament in front of me as I sit and write this blog. They are taking my case on and written to my surgery which have let me down so dreadfully! I bet I get that injection now?! I hope this blog helps others. Stay strong and don't keep quiet and don't hide away.
Peace, love and light. Never take anything for granted. Even your skin!
Sonya Roseman (Actress) July 8th 2016 x
