It is my sincere hope that you will never need to use CaringBridge. It’s a web-based service that helps the families of people who’ve suffered a medical crisis set up a simple website and blog to keep friends up-to-date. While many people are on Facebook these days, there are still quite a few who don’t care to join. Having a single place like CaringBridge where everyone can check to see the latest news about an ailing friend or family member is really useful.
I’ve recently been serving as the administrator of a CaringBridge site for my friend Stu, who had a severe stroke in mid-June. While the system is technically quite easy to use, it turns out that the communications work itself requires some thought. On one hand, I’m serving an audience that has lots of questions and comments. On the other hand, I’m assisting Stu’s partner and need to be attuned to her perceptions and honor what she wants to communicate and when.
After three months of working with CaringBridge, I’ve come up with a five tips that I believe can make the service slightly easier for other people to use. Karen asked me to share them here at WriterWay.
- Have a CaringBridge account set up quickly after a medical catastrophe.
- Have someone other than the primary caregiver administer and manage the site.
- Update the site’s journal regularly and honestly.
- Update the original information (on the main story page) to reflect major changes.
- Keep your audience in mind.
For those of you interested in more, I’ll expand a bit on each of the five points:
1. Set up a CaringBridge account quickly after a medical catastrophe.
Speed is important. People want to know where to go for information, and having a CaringBridge site ready quickly makes a big difference in whether people will go there for information. I’d guess the window for getting a site started is between an hour and 72 hours after the event. Don’t wait to be certain whether you’ll need it: if the person is going to be in the hospital overnight or longer after an emergency, that’s a pretty clear indicator that people will want to know about it. And if the condition is imminently life-threatening (certain types of cancer, for example), you’ll want to start rallying support.
2. Have someone other than the primary caregiver administer and manage the site.
The primary caregiver is going to have his/her hands full dealing with the medical situation, and perhaps insurance issues and visiting relatives. Friends will ask what they can do to help. Someone with a combination of computer skills and people skills is the ideal person to ask to set up a CaringBridge site. CaringBridge is pretty easy to use for anyone experienced with online groups. In fact, if you’re reading this, you probably have the necessary skills to set up an account.
3. Update the site’s journal regularly and honestly.
People will come to the CaringBridge because they want to know what’s going on. A regular schedule is very helpful. I posted daily during the period when my friend was in Intensive Care from the stroke; when he moved to rehab, I noted that the posts would get less frequent. When he had to go back into the hospital, I increased the frequency. And if something major happened, positive or negative, I’d stick in an extra post.
It’s also important to be honest. If you don’t know something, say so. Things are going to be uncertain more often than they’re going to be clear. People still want to hear. And if something bad happens, say so. Don’t hope it will go away if you ignore it. It may go away (which gives you good news to post), but your talking about it won’t hasten that or give it extra power.
4. Update the original information (on the site’s My Story section) to reflect major changes.
A CaringBridge site has a top section called “My Story” where you can write a very short summary of what’s going on. Remember to update this summary when something major changes. I posted that my friend had had a stroke: two weeks later, folks coming in to read what was happening thought that this meant he’d had another one. Oops. Adding the date took care of this problem. Saying when he moved to rehab also helped keep things clear. This section is limited in length to a few hundred characters. It’s not Twitter, but it’s a place to be very concise.
5. Keep your audiences in mind.
If you’re the designated manager of the site, you have two very important audiences. The first is the primary caregiver. Your goal is to help him/her get all the information into a small package, figure out what her/his friends will want to know, and write it down. There will be things that it’s not appropriate to talk about (reactions of some visitors, other people’s fears, and such). Talking things out with the primary caregiver also helps him/her gain some perspective on what’s going on. Don’t be afraid to ask “How do we want to present this?”
The other audience is the people who want to find out what’s going on. Tell them as much as you can without either writing too much (1000 words per update is Too Much Information unless there’s something complex and specific to say) or saying inappropriate things. Sometimes you should push the primary caregiver to say a bit more, but don’t insist: S/he is the one who has the most to say about what happens on the CaringBridge site. Remember to appreciate people who give you feedback about how the site is going, and don’t reject ideas that might improve your site management. Sign your updates so people know who is making the updates. Be accessible. Read the Guestbook comments to make sure no one is misinterpreting your journal posts.
It takes a village to deal with a major illness. If you’re managing the CaringBridge account, you’re the village reporter. It’s a serious and rewarding job.