I am a web designer but nothing I have designed has come this easy and this fast but here’s the issue….. I have no one to show this to. This is why maybe this is so needed. I know no one personally that I can discuss MCAS issues, triggers, symptoms, medications, and just plain how to deal with it. I have seen articles, talked with doctors (one who is a specialist in MCAS and others who do not know about this), and my nurse who is really helpful and now really full with her practice.
So who do you turn to????
That’s the point. We all could use someone to lean on, someone to call an MCAS buddy, someone who “gets us”.
I’m writing this because I am a bit scared to put this out into the Universe. Will it be accepted well or will anyone take offense to it…. I don’t know and I don’t have anyone to ask.
As Adelle sings – go easy on me. I’ll do my best and let the Universe do the rest.
