NOVEMBER 2019 - New Members
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
NOVEMBER 2019 - New Members
Friday, November 1
Welcome to
CLARK0605, who has been affected with RLS for the past 15 years, since her daughter was born. She had good luck with DA drugs (ropinerole and then pramipexole) until she started having major middle of the night insomnia about 3-4 years ago. Made the decision to gradually switch to pregabalin and had her last dose of pramipexole on Oct 12th. Having a pretty difficult time at the moment and hoping to get some help/support/ideas on way forward.
Pregablin isn't strong enough to cover the withdrawal from pramipexole, but you are over the worst of it and things will generally improve. Some of us are able to get along with just pregablin or gabapentin following DA augmentation while others of us require an opioid to treat our RLS.
Please feel free to post a note with any questions that you have or simply join one of our existing discussions.
Welcome to
CLARK0605, who has been affected with RLS for the past 15 years, since her daughter was born. She had good luck with DA drugs (ropinerole and then pramipexole) until she started having major middle of the night insomnia about 3-4 years ago. Made the decision to gradually switch to pregabalin and had her last dose of pramipexole on Oct 12th. Having a pretty difficult time at the moment and hoping to get some help/support/ideas on way forward.
Pregablin isn't strong enough to cover the withdrawal from pramipexole, but you are over the worst of it and things will generally improve. Some of us are able to get along with just pregablin or gabapentin following DA augmentation while others of us require an opioid to treat our RLS.
Please feel free to post a note with any questions that you have or simply join one of our existing discussions.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to JGrace
Friday, November 1
Welcome to
JGrace, whose RLS has affected her sleep so that she is tired in the day time. She also has problems getting used to Ropinirole.
Please tell us a bit about your issues with ropinirole so that we can have an idea of what to suggest to you. And feel free to ask any questions that you have.
Welcome to
JGrace, whose RLS has affected her sleep so that she is tired in the day time. She also has problems getting used to Ropinirole.
Please tell us a bit about your issues with ropinirole so that we can have an idea of what to suggest to you. And feel free to ask any questions that you have.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to RPO
Saturday, November 2
Welcome to
RPO, who has difficulty sleeping and has to get up and sit in a chair 1-2 times a night
Please post a note telling us what you are currently doing to treat your RLS so that we can offer you some suggestions to get a full night's sleep.
Welcome to
RPO, who has difficulty sleeping and has to get up and sit in a chair 1-2 times a night
Please post a note telling us what you are currently doing to treat your RLS so that we can offer you some suggestions to get a full night's sleep.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to sliderdkp
Saturday, November 2
Welcome to
sliderdkp, who says that RLS and the treatments are horrible.
Please post a note telling us about the treatments that you have tried and the issues that you had with each so that we can offer you some suggestions for improvement.
Welcome to
sliderdkp, who says that RLS and the treatments are horrible.
Please post a note telling us about the treatments that you have tried and the issues that you had with each so that we can offer you some suggestions for improvement.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to RLS43
Sunday, November 3
Welcome to
RLS43, who has had RLS for over 20 years and is always interested in new & innovative treatments and also with breakthrough RLS treatments.
Please post a note telling us about your current treatment and asking any questions that you have. Also take a look at the Research discussion thread in the General Topics forum to get an idea of the latest research work.
Welcome to
RLS43, who has had RLS for over 20 years and is always interested in new & innovative treatments and also with breakthrough RLS treatments.
Please post a note telling us about your current treatment and asking any questions that you have. Also take a look at the Research discussion thread in the General Topics forum to get an idea of the latest research work.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to Homestarmy
Sunday, November 3
Welcome to
Homestarmy, who has suffered with RLS for almost thirty years and, for the vast majority of that time, he dealt with it alone. He takes 600mg of gabapentin along with 2mg of mirapex and his symptoms aren't controlled; his nights are a hell of exhaustion and involuntary movement. He is augmented, and tried covering with a 3rd mg of Mirapex, but that failed as well. Two weeks ago he stumbled across a miracle device that completely alleviates his symptoms, and he wants to get the word out because, despite a couple of small positive research studies around 2007 - 2010, this seems to be completely unheard of. He is using a PCD (pneumatic compression device), and it is amazing. He wants to share that with anyone who will listen.
As you said, pnuematic compression is something that has been around for a while. It doesn't work for everyone, but it does help some. Glad that you are one of the ones who benefits from this device.
Welcome to
Homestarmy, who has suffered with RLS for almost thirty years and, for the vast majority of that time, he dealt with it alone. He takes 600mg of gabapentin along with 2mg of mirapex and his symptoms aren't controlled; his nights are a hell of exhaustion and involuntary movement. He is augmented, and tried covering with a 3rd mg of Mirapex, but that failed as well. Two weeks ago he stumbled across a miracle device that completely alleviates his symptoms, and he wants to get the word out because, despite a couple of small positive research studies around 2007 - 2010, this seems to be completely unheard of. He is using a PCD (pneumatic compression device), and it is amazing. He wants to share that with anyone who will listen.
As you said, pnuematic compression is something that has been around for a while. It doesn't work for everyone, but it does help some. Glad that you are one of the ones who benefits from this device.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to ninoescofet
Monday, November 4
Welcome to
ninoscofet, who was recently diagnosed with RLS. Nino would like to hear about other people's experiences and would like to learn more about various medications and treatment options.
Please post a note telling us what you are currently doing to manage your RLS so that we can have an idea of where to start with explanations about the various treatment options open to you.
Welcome to
ninoscofet, who was recently diagnosed with RLS. Nino would like to hear about other people's experiences and would like to learn more about various medications and treatment options.
Please post a note telling us what you are currently doing to manage your RLS so that we can have an idea of where to start with explanations about the various treatment options open to you.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to MKoz
Tuesday, November 5
Welcome to
MKoz, who was diagnosed with RLS over twenty years ago and has seen and experienced a lot in those years.
Please post a note telling us a bit about your RLS experiences over those 20 yrs.
Welcome to
MKoz, who was diagnosed with RLS over twenty years ago and has seen and experienced a lot in those years.
Please post a note telling us a bit about your RLS experiences over those 20 yrs.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to michebjerke
Friday, November 8
Welcome to
michebjerke, whose husband has severe RLS and she wants to help him with treatments and support.
Please post a note telling us about his treatments and asking any questions that you have so that we can provide some of the support that you are looking for.
Welcome to
michebjerke, whose husband has severe RLS and she wants to help him with treatments and support.
Please post a note telling us about his treatments and asking any questions that you have so that we can provide some of the support that you are looking for.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to Hoknott
Saturday, November 9
Welcome to
Hoknott, who was diagnosed with WED/RLS in 2004. After menopause etc she required medication. She has a doctor who specializes in sleep disorders & follows Dr Earley. Before treatment, she was suicidal from sleep exhaustion & coping with physical symptoms.
Please post a note telling us about your medication and asking any questions that you have.
Welcome to
Hoknott, who was diagnosed with WED/RLS in 2004. After menopause etc she required medication. She has a doctor who specializes in sleep disorders & follows Dr Earley. Before treatment, she was suicidal from sleep exhaustion & coping with physical symptoms.
Please post a note telling us about your medication and asking any questions that you have.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to jillyand40
Tuesday, November 12
Welcome to
jillyand40, who says that it may seem to normal people that RLS is not a big deal...but it is. jilly has been trying to sleep for 5 hours tonight and is still awake with what jilly calls...jumpy legs. it is very aggravating and depressing.
Sleep deprivation is something that most of us have learned to live with. Please post a note telling us what you are doing to manage your RLS so that we can offer you some suggestions to discuss with your doctor.
Welcome to
jillyand40, who says that it may seem to normal people that RLS is not a big deal...but it is. jilly has been trying to sleep for 5 hours tonight and is still awake with what jilly calls...jumpy legs. it is very aggravating and depressing.
Sleep deprivation is something that most of us have learned to live with. Please post a note telling us what you are doing to manage your RLS so that we can offer you some suggestions to discuss with your doctor.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to Lbrick
Tuesday, November 12
Welcome to
Lbrick, who has had RLS for a good 40 years now and is getting desperate for help. Mute Dr’s don’t seem to know what to do so she feels she is on her own. She doesn’t sleep and is embarrassed to be in a relationship because they think she is crazy! This has taken over her life for years now and she is miserable!
Please post a note telling us what your doctor(s) have prescribed and what you are currently taking. We can offer you some suggestions, including how to find a doctor who understands and will help.
Welcome to
Lbrick, who has had RLS for a good 40 years now and is getting desperate for help. Mute Dr’s don’t seem to know what to do so she feels she is on her own. She doesn’t sleep and is embarrassed to be in a relationship because they think she is crazy! This has taken over her life for years now and she is miserable!
Please post a note telling us what your doctor(s) have prescribed and what you are currently taking. We can offer you some suggestions, including how to find a doctor who understands and will help.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to walkerwear
Tuesday, November 12
Welcome to
walkerwear, whose husband has severe RLS in all limbs and rarely sleeps. He has tried so many meds, but there's always augmentation in the end to reset his progress to zero.
Please post a note telling us which meds he has tried. There are very effective meds that do not lead to augmentation. We know because most of us have been there too.
Welcome to
walkerwear, whose husband has severe RLS in all limbs and rarely sleeps. He has tried so many meds, but there's always augmentation in the end to reset his progress to zero.
Please post a note telling us which meds he has tried. There are very effective meds that do not lead to augmentation. We know because most of us have been there too.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
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- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to Ata
Tuesday, November 12
Welcome to
Ata, who has had RLS for about 4 years and it has been a total obstacle and disruption to life.
Please post a note telling us what you are doing to manage your symptoms so that we will know what sort of things to suggest to you to remove those obstacles and disruptions.
Welcome to
Ata, who has had RLS for about 4 years and it has been a total obstacle and disruption to life.
Please post a note telling us what you are doing to manage your symptoms so that we will know what sort of things to suggest to you to remove those obstacles and disruptions.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
-
- Moderator
- Posts: 6513
- Joined: Sat Sep 28, 2013 9:31 pm
- Location: Colorado Springs, Colorado
Welcome to Cookie
Wednesday, November 13
Welcome to
Cookie, whose RLS runs in her family. Her father suffered terrifically 50 years ago. Without medication, she would never sleep and now has learned her teenage granddaughter is being to have bouts. She would like to learn more about treatments, new research, and possible non-pharmacological treatments.
Take a look around to get an idea of the variety of treatments that are available, and feel free to post a note with any questions or comments that you have.
Welcome to
Cookie, whose RLS runs in her family. Her father suffered terrifically 50 years ago. Without medication, she would never sleep and now has learned her teenage granddaughter is being to have bouts. She would like to learn more about treatments, new research, and possible non-pharmacological treatments.
Take a look around to get an idea of the variety of treatments that are available, and feel free to post a note with any questions or comments that you have.
Steve
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.