So ive been thinking about writing this blog post for a long time because although there is a lot of information about my illness on the internet, there isnt many posts from people giving there view on living with it.
So since the age of 18 years old i have been living with a condition called Hypothyroidism, i had never heard of a thyroid before so i was shocked to find out that i had something wrong with mine.
Hypothyroidism means that your thyroid gland doesnt produce enough of the hormone needed which can cause you to feel tired, depressed, to have dry skin and hair, sensitivity to the cold and may cause your muscles to ache.
A lot of people dont realise they have this condition as they ignore symptoms or dont realise they have them. I was the same. I had all these symptoms but i had no idea until one night my vision completley disappeared and my eyes started to shake, i was rushed to hospital but with no conclusive answers i was sent home that night. This happened three more times before i finally went to my local GP who decided to run some more in depth blood tests than i had done at the hospital which showed up that my TSH levels were normal but my T4 levels were abnormal which led to me being diagnosed with this illness.
I currently take 50mg of levothyroxine daily and have done since i was first diagnosed which although its a small dosage makes so much of a difference to my life. I always thought i would live this energtic life running round, chasing Albie, playing sports with him but sometimes i find it hard to even have the energy to get out of bed but i do and he really is the reason i get out of bed and do the things that we do together.
People always say to me you look so well and happy all the time, but they dont see how hard some days are, how exhausted i can be and how drained i am if i dont take my medication. Some days are harder than most but its something ive learnt to deal with and although i do have bad days i also have really good days where i do feel that there is nothing wrong with me. Taking my medication doesnt mean my life is back to normal and i do still experience episodes wear i lose my sight which doesnt happen to all people with this condition but it does to me.
Just because somebody looks well and happy, doesn't necessarily mean they are. Never judge someone by what you see on the outside because you never know what is happening on the inside, always remember that.
Hope this helps some of you who have an invisible illness or know somebody who does. Let me know in the comments if have an illness and what it is and how you deal with it.