Sophia

My experience has been a stressful and hectic one the moment i was diagnosed of LC.

I've been sick for 6 years already and it has indeed changed my abilities as well limited my daily activities generally, to be sincere i wouldn't wish my enemies what I've been through. 

The process of getting diagnosed was frustrating at first not until my friend suggested a virtual options for my follow up. I have leant life is more precious and valuable because sick or diagnosed with LC will never make life better except maybe there's a research study to prove and execute that.

Looking good doesn't always mean feeling good.

 Finding support and treatment at first was difficult not until a friend of mine who suffers the same sickness gave a virtual options which really helped me out then to arrange for my treatment overtime.