Psoriasis since Oct 2017. Learning fast! Also have Trigeminal and Occipital Neuralgia and severe nerve damage in my leg. Mostly bed bound and only leave the house for hospital appointments. My partner and my Son keep me going.
Nikki, that is what we are here for, to support each other. All questions are welcomed. I am so sorry you are going through this right now. I really hope your tablet gives you some relief. A lot of people find relief with them. Have you ever looking into biologics? They seem to really help others who have been severe. Take a look at the themes section for them to get a better idea. I believe it was Damien who shared that he puts dead sea salts in a spray bottle with water. I wonder if that type of spritz spray could be helpful. Try and have hope that your tablets will help. I know its hard..but try and reach for even a little bit of hope.
Please dont apologize for your post. I am happy you have reached out. I hope things can get better soon! ❤ xx
Hi Michelle, I am on biologic infusions every 2 months. Introveniously administered. I am lead to believe Biologics hunts out the cells that want to attack my body, coats them and basically tells them to go yo sleep.
I am 70% better beca use of it! The biologic I am on is 30% mouse protein, and I must say my desire for cheese has increased some what. If it gets to the point where I want to hide under the bed when I see a cat, I'll have to talk with my specialist. Lol
My ankles. Whenever I get a flare up and new spots appear on the side of my ankle, I can never hide it. It always turns blue when its a bit overcast outside or when I am in an office with an aircon. People stare especially when they don't know what it is and it makes me angry because why the heck do I have to explain myself (condition) again? It's frustrating. So now I treat my whole body just in case I might get P on my feet and I refuse to wear boots in summer.