Saturday, December 29
Welcome to
sford0202, who has suffered from RLS for sford's entire life, as does sford's father, and as did his mother. sford suffers from side effects of Mirapex but can't lie down at all without that drug. sford would love to share stories, ideas, and find support.
Please post a note telling us about the dose and side effects that you are experiencing with Mirapex so that we can offer some suggestions for improving your situation.
DECEMBER 2018 - NEW MEMBERS
Welcome to sford0202
Steve
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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.
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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: 7648
- Joined: Tue Dec 26, 2006 4:34 pm
- Location: N. Ireland
Welcome louis1m
Welcome to
lousis1m - who feels he has had this condition since birth and is trying to find coping mechanisms as it appears to be getting worse. Sleeping, reading, transportation are issues needed to be dealt with on a daily basis.
Please post and tell us about your current treatment, we understand and want to help.
lousis1m - who feels he has had this condition since birth and is trying to find coping mechanisms as it appears to be getting worse. Sleeping, reading, transportation are issues needed to be dealt with on a daily basis.
Please post and tell us about your current treatment, we understand and want to help.
Betty
http://www.willis-ekbom.org/about-rls-wed/publications
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation
http://www.willis-ekbom.org/about-rls-wed/publications
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation
Welcome to rlsgal70
Sunday, December 30
Welcome to
rlsgal70, who has RLS & iron deficiency. She is unable to take iron supplements because it causes constipation. Life is hell
You sound like a good candidate for an iron IV treatment. These are a relatively new development in the treatment of RLS. If your doctor is not familiar with these, post a note and we can point you to documents that you can share with him/her.
Welcome to
rlsgal70, who has RLS & iron deficiency. She is unable to take iron supplements because it causes constipation. Life is hell
You sound like a good candidate for an iron IV treatment. These are a relatively new development in the treatment of RLS. If your doctor is not familiar with these, post a note and we can point you to documents that you can share with him/her.
Steve
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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.
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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.
Welcome to msmorning
Sunday, December 30
Welcome to
msmorning, who is not able to take a nap or get a restful night sleep due to RLS. msmorning is desperate for relief and wants to stop using ropinerole.
Please post a note telling us about the dose of ropinirole that you are taking and how long you have been on this dose so that we can offer some things to discuss with your doctor.
Welcome to
msmorning, who is not able to take a nap or get a restful night sleep due to RLS. msmorning is desperate for relief and wants to stop using ropinerole.
Please post a note telling us about the dose of ropinirole that you are taking and how long you have been on this dose so that we can offer some things to discuss with your doctor.
Steve
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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.
Augmentation Evaluation http://bb.rls.org/viewtopic.php?f=4&t=9005
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.
Who is online
Users browsing this forum: No registered users and 1 guest