Dealing with HCM and more.
First post.

So this is my first blog post, it’s currently nearly 4am in the morning, and I finally decided to make this blog - I wish I had a real reason for wanting too other than I feel like it’d be a good way to let out my emotions and the highs and lows of having to deal with the things I deal with on a daily basis while living with HCM. I think, the thing is, with HCM, it comes in so many different forms, and no-ones experience with it is the same, and I guess thats the same with all diseases really, everyone deals with the diagnosis and the effects of the disease in different ways, but we can all relate and try to help, even with those who have something different wrong with them, there’s always that relation there - of having something wrong and having to deal with it each day.

I often find myself thinking and day-dreaming about what “could” happen to me with HCM, instead of thinking about the now, and what I could be doing instead of thinking about what could happen to me in life - because there’s no point dwelling on something that can’t be changed - you can’t change the diagnosis, but you can learn to live with it, and I guess that’s the point of this post particularly - is to know that life goes on after diagnosis of something like this, and that things will be difficult, and you will face trials - but you will also come out much stronger, so that’s the message of this post, be strong, be positive, be okay, because  things do go on, life goes on, and so do you.