Support. When I started this MM series of posts, I did have some goal(s) in mind. I thought, after perusing forums, boards, other Cancer sites I had experiences after 4 yrs of MM others might find useful.
Therapeutic. I have found myself fighting this MM funk and had yet to find a way through it. Each and every step required a reserve of energy, which, other than the doing of a thing, had nothing to do with the thing itself.
Information. I found, what I thought, too many posts & responses to be of a shallow character, not really, to my mind, either answering the question, or answering in a way that would give useful info. ( I am much aware of why this is so) There is so much info about MM available, as well as a lot of BS, I think it important to offer solid info and give others the chance to use as they can.
HOPE. Many inquiries come from folks after initial diagnosis. Surprise!!! You have Cancer!!! I believe a primary need at this point is to offer HOPE. And there is much HOPE for living with MM. All the info, protocols, etc mean squat without HOPE. The MM is manageable. The Garden of HOPE has to be sown and cultivated.
The chronological order I had tried to impose on my MM experiences very quickly fell apart. Memory is an elusive and tricky adversary. I may start with a specific memory but inevitably I am led through the Neuronal Maze (hence Neuronal Catastrophe) of MM memories, ending far afield from where I thought I would be. I knew this was a game I had little chance, or desire, of playing. I apologize for the randomness of my posts for the 1 or 2 who pay attention. What is written here is the complete truth, at least to the extent mind reveals it as I write.
Shared Pain Lessened
Shared Joy Increased