Support for those with invisible Illnesses

Hi! This blog is simply for those with an invisible illness to talk about their experiences and talk to one another to find support.
cfsucksair: I havent seen a comparison of CF lungs and healthy lungs in a VERY long time. But it’s mind blowing that we can still function with all of the scaring that some of us can have.

cfsucksair:

I havent seen a comparison of CF lungs and healthy lungs in a VERY long time. But it’s mind blowing that we can still function with all of the scaring that some of us can have.

(via cfsucksair-deactivated20120618)

Sorry for being gone again!

Everything just kind of becomes too much and blogging about my illness is sometimes the last thing I need.

But my prozac dose has gone up again and i’m feeling a bit better after going through a bit of a rough patch.

I’ll try to post regularly again now :)

Also, I’ve finally got my appointment about changing to Hydrocortisone from Prednisolone, so fingers crossed that goes well!

foreverfatigued:

Life with a chronic illness is so fun.

I mean, who doesn’t enjoy being forced to lay in bed for weeks straight?

Who doesn’t like those nights where you’re so tired you cant sleep?

Losing all your friends because they dont understand is SO fun.

Having to convince doctors that your pain is real is always enjoyable.

Oh, and what about all that soreness and pain? It’s so lovely.

Fuck being ill.

(via chronically-something)

I felt this was relevant, because as well as disabled people, I know a lot of ill people feel this way too. Stairs really exhaust me, I’m so happy there are lifts at the college I’m going to.

I felt this was relevant, because as well as disabled people, I know a lot of ill people feel this way too. Stairs really exhaust me, I’m so happy there are lifts at the college I’m going to.

(Source: gissell, via aimsme)