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Re: RLS Foundation hosting a Patient Symposium

Posted: Sat Aug 25, 2018 10:06 pm
by Polar Bear
Dreams are what keep us going. :D

Re: RLS Foundation hosting a Patient Symposium

Posted: Mon Aug 27, 2018 7:54 am
by Yankiwi
Too far for me too—6,500 miles—but it will be wonderful to hear about it.

Re: RLS Foundation hosting a Patient Symposium

Posted: Tue Aug 28, 2018 12:32 am
by jewelsong
Speaking of hearing about it ... will there be recordings or transcripts of the talks available afterwards on the website? For multiple reasons, I will not be able to attend.
Blessings to all of you. Reading your stories and wisdom keeps me sane with this wretched disease.

Re: RLS Foundation hosting a Patient Symposium

Posted: Tue Aug 28, 2018 12:44 am
by Rustsmith
jewelsong, that is a good question. I will call the Foundation office tomorrow and let you know what they say.

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Aug 30, 2018 6:34 pm
by Rustsmith
I have been told that due to budget constraints, they are not currently planning to record or transcribe the proceedings. They are also not planning to make the slides available.

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Aug 30, 2018 9:47 pm
by ViewsAskew
Rustsmith wrote:I have been told that due to budget constraints, they are not currently planning to record or transcribe the proceedings. They are also not planning to make the slides available.


Too bad. Would be nice if there were some less expensive recording and storage options.

Re: RLS Foundation hosting a Patient Symposium

Posted: Sat Sep 01, 2018 4:34 am
by Yankiwi
Our discussion board attendees can give us a rundown.

Re: RLS Foundation hosting a Patient Symposium

Posted: Sun Sep 02, 2018 8:46 am
by sleepdancer2
Anyone in Los Angeles making the 2+ hour drive down?

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Sep 06, 2018 4:38 am
by ViewsAskew
sleepdancer2 wrote:Anyone in Los Angeles making the 2+ hour drive down?


I am in LA and am thinking about it. Given how crazy my legs can be, I am getting averse to scheduling things...

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Sep 06, 2018 2:59 pm
by Rustsmith
For what it is worth, I am planning to fly to San Diego to attend the symposium. I will try to take notes and post a brief summary upon my return home.

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Sep 06, 2018 5:29 pm
by Oozz
Is this the first symposium? I’m wondering what will be covered that isn’t readily available online...

Re: RLS Foundation hosting a Patient Symposium

Posted: Thu Sep 06, 2018 6:46 pm
by Rustsmith
This isn't the first patient conference, but it is the first one in a long time. As for what will be covered, most of info in the presentations is probably already available either through the research papers, Nightwalkers, the webinars or even You Tube. What will be most interesting, at least to me, will be the interaction between the participants with RLS and the doctors/researchers, especially during the breaks and meals. Drawing from my experiences at my professional conferences, this is when the really interesting conversations happen. In these "social" conversations, the doctors are free to talk in speculative terms and say things like "I think ....", which they cannot do in print. As for patients, you never know when one of us says something followed by others agreeing, which tells the doctors something they didn't know before. An example might be something like a "conversation" we had here a number of years ago about how many of us can stand to touch things that are hotter than others, or immerse ourselves in water that others find to be "scalding". I know that one question that I want to ask Dr Ferre is what sorts of currently used meds, other than dipyridamole, that he thinks might also be helpful. This interests me because I suspect that my low heart rate and low blood pressure would make me a poor candidate for dipyridamole.

Re: RLS Foundation hosting a Patient Symposium

Posted: Fri Sep 07, 2018 6:48 am
by sleepdancer2
@ViewsAskew Do you live in LA now? I hear you about it being hard to plan.

@Rustsmith I think I would thoroughly enjoy this meeting. The interactions you describe appeal to me a lot. I have always wished more doctors could know a couple things about my journey, as it could possibly help someone somewhere. #1 That after getting past augmention and getting of the DAs that my legs are controlled by using TENS. and #2 That abrupt stopping of a DA from a high dose caused synesthsia. Patients who are the outliers seem to get lost in the mix.

Re: RLS Foundation hosting a Patient Symposium

Posted: Tue Sep 11, 2018 5:33 am
by ViewsAskew
sleepdancer2 wrote:@ViewsAskew Do you live in LA now? I hear you about it being hard to plan.

@Rustsmith I think I would thoroughly enjoy this meeting. The interactions you describe appeal to me a lot. I have always wished more doctors could know a couple things about my journey, as it could possibly help someone somewhere. #1 That after getting past augmention and getting of the DAs that my legs are controlled by using TENS. and #2 That abrupt stopping of a DA from a high dose caused synesthsia. Patients who are the outliers seem to get lost in the mix.


Yes, I do.

Re: RLS Foundation hosting a Patient Symposium

Posted: Mon Oct 01, 2018 11:32 pm
by Oozz
So, who is gonna debrief us on all the cool stuff that was discussed at the symposium? :D