Friday night I will be having dinner with family members I have never met who have CCM. Joining us will be the Ambassador of Angioma Alliance, who was the first to start an Awareness Program for this disease about 10 years ago when her daughter was diagnosed with CCM.
I am so excited!

About these ads

Posted by on February 3, 2012 in Daily life with this disease....

Leave a Comment

About melessia

A woman who suffers from CCM (Cerebral Cavernoma Malformations). This blog is to bring Awareness to a much overlooked disease.l

Leave a Reply

Fill in your details below or click an icon to log in:

Gravatar
WordPress.com Logo

You are commenting using your WordPress.com account. ( Log Out / Change )

Twitter picture

You are commenting using your Twitter account. ( Log Out / Change )

Facebook photo

You are commenting using your Facebook account. ( Log Out / Change )

Cancel

Connecting to %s