It happened again. For the second time since starting this blog, a prostate cancer support group reached out and asked me to be a featured guest at one of their support group meetings. The first was five years ago in Riverside, California, and the second happened last night via Zoom. I have to admit that I was both surprised and humbled by each request.
The facilitator for the North Vancouver (British Columbia, Canada) Prostate Cancer Support group, Jeff, contacted me to spend an hour or so having a conversations about my blog and my personal experience with prostate cancer. (The group is affiliated with the Prostate Cancer Foundation Canada and they offer a number of support groups across the country. You can learn more HERE.)
The event was billed as “A Conversation with Dan,” and around a dozen fellow prostate cancer patients attended. Jeff, the facilitator asked a series of questions to get the conversation going, and by the end of the hour and forty-five minutes, most everyone was engaged in the conversation sharing their own stories and insights or asking questions. It was (from my perspective) an informative and enjoyable evening.
Thank you, Jeff, for contacting me and suggesting the idea, and to everyone else who made me feel welcome through your participation.
That leads me to the general topic of support.
When I was first diagnosed, I relied on the support of my family, friends, and a few other prostate cancer patients that I was introduced to simply by me being open about my diagnosis. Their support was invaluable to me.
As time went on, I did seek out an in-person support group here in San Diego. I did find one, but it was very small with only a few members and it was more of a social group that liked to gossip than a place to learn about prostate cancer. I thought I could offer insights on my own experience, but the members were so far ahead of me in their own journey that they had already “been there, done that.” Needless to say, I didn’t find much value and stepped away from the group.
Instead of in-person groups, I turned to support and insights from two sources.
The first and most valuable to me has been you, the readers of this blog. Even though I’ve never met most of you in person, I appreciate those of you who have shared your own stories and feedback. Thank you.
The second source is from the website Malecare.org and the prostate cancer forums there. There are some very knowledgeable people in those forums who are willing to share a ton of information and experiences. (There’s a gentleman who goes by the screen name Tall_Allen who is a fountain of knowledge, and has two online sources of information: Prostate Cancer News and Prostate Cancer Infolink.)
I know that I’ll have much to learn in my new post-ADT/SRT world, so I spent some time today searching the major prostate cancer nonprofits for prostate cancer support groups in the San Diego area, and was surprised by the lack of in-person groups:
- ZERO Prostate Cancer / US Too has a group in Fullerton, California, two hours away.
- The Prostate Cancer Foundation lists only online Facebook support groups (which I’m a member of one).
- The Prostate Cancer Research Institute had a lengthy list of resources, but virtually all were provided by other groups.
- The American Cancer Society was particularly limited in what they offered.
But there was one that’s in the San Diego area that looks promising. It’s called the Informed Prostate Cancer Support Group. The website has a lot of information with videos of their past meetings in case you couldn’t attend. Their meetings are held in an auditorium with quite a few members, which may stymie personal sharing and conversations.
That’s the one thing I liked about last night’s group. It was small enough that those conversations could be had and, even after just an hour or so, I could tell there was a bond between the members. I don’t know that you would get that in a larger group setting.
I’ll continue to do more searching but perhaps my new mission in life may be to work with an organization to form a “Goldilocks” group here in San Diego—not too small like the first one I joined, and not too large so there’s no personal interaction. Hmm… I’ll have to think about that. Between keeping this blog going and running a support group, all prostate cancer, all the time could get to be a bit much. But if it does help others… 🤔 Stay tuned.
The main take-away from all of this is that it’s okay to seek support, no matter where you are in you diagnosis and treatment. Whether it’s from family, friends, in-person support groups, or online forums (including silly blogs), the support and education you’ll receive by reaching out will ease the burden.
Again, thanks to Jeff and all the men at the North Vancouver Prostate Support Group for inviting me to participate. I truly enjoyed the experience.
Header Image: Sunset at Cape Flattery, Washington State
8 thoughts on “Let’s Talk II: The Importance of Support”
Thank you, Dan. Your blog was a huge source of comfort for me when I was diagnosed. I’m glad to see you’re taking it to the next level now, too.
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Thanks Dan, we enjoyed it as well.
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Dan, what a pleasure and honour we enjoyed having you speak to our group yesterday! Thank you again!. I had some great feedback from the group as we all enjoyed your candor and the discussion. I think I can speak for all of us PC survivors, we so appreciate your blog and how you put yourself out there to share your journey, your struggles, the ups, the downs, the DATA!!, and just the brutal honesty and humour with which you share it all. Keep doing what you are doing!! Cheers, Jeff
Thank you forvthe links
Thanks for talking to our group In N Vanc . James from Vancouver Island here . Sorry I missed you . Darn ! We have written each other over time and I would have liked to be there with my Brothers from the area. In SE Asia right now( Indonesia, Malaysia, and Now my place in North Luzon) . I am in a remote place , comfortable , near the jungle edge . Problem is the Internet is unstable and the 3G for video is weak ! The down side of my place I gather ….But there are many up-sides! 🙂 . Back on Vanc. Island on May 01…hopefully we can link-up ! Thanks again for your time Dan . James – Vancouver Island ( currently North Luzon )
I was one of the participants for the North Vancouver support group. Thank you for your presentation. I was also diagnosed 13 years ago but I have been on Active Surveilance ever since. I continue to have quarterly PSA and have had 7 biopsies. I presume that some day I will need treatment.
Wow! It seems like every time I post something about prostate cancer, one of these support groups bothers to reach out. It’s great to see that there are people out there who care about helping others, and it’s even more amazing when they’re reachable. Thanks for being part of the community!
Jus thought Iâd reach out across the Ocean and let you know Iâve now complete Hormone and RT and had my first post-treatment bloods done.
div>All the results are fantastic, PSA is