Sorry Margo, that is not my intent. There are unfortunately still very few options of places to go and talk. I really wish there was more choices and more knowledge that we could draw from. I know support groups are not for everyone, the term alone puts some off. Over the 9 years it has been difficult finding others to talk to, getting doctors support for this group and finally difficulties getting a hospital venue afterhours, this resulted in meeting at others homes. There is a great need by people diagnosed with pc for support given the severity of the condition, the frightening odds and I remember too well the devestating feeling of being alone facing this. Yes, we need to be able to talk to each other, and I want as many options for others as possible, phone, email or face to face. We all have different needs in this journey and in order to make good choices for ourselves and our families we need to know what is available. We are very fortunate at this point in time as we have a "greenfields" position and we can lay the groundwork for others yet to come. What do others want our support choices to look like?
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