Am I disabled according to the social model?

Hi!

I came across Scope today.

I was doing a bit of research for my newly resurrected blog, 'Don't dismiss M.E', and I found myself asking the quesion, "How do I know that Iam disabled?". Then I found myself here!

I have ME/CFS, fibromyalgia, celiacs disease and lichen planus, another auto immune condition.

I've been ill for 9 years and have slowly and at times quickly deteriorated in my illness.
Iam currently 100% house/bed bound. Normally, I am in the range between 85-90%. 

Have I answered my question? Am I disabled? The answer is yes and yes! But, mine like so many others is one that is invisible to the world. When I am out and in my wheelchair, people can see me, or not as I've found! There really should be a law about people walking and looking down at their phones as I've had many people almost land on my lap despite my shouts of "four" (golfing term )!!

But, what I do not have the answer to is this. If I am housebound and not out and about, then am I still disabled? If our impairements prevent us from accessing the outside world, then can we call ouselves disabled according to the social model?

Answers on a postcard please!

Nice to meet you all. x