Went to U of M...changing meds again
Posted: Thu Aug 29, 2013 1:26 pm
I had my appointment at U of M with the sleep doctor. Finally a doctor that actually seems to understand this disease. She went through the whole thing explaining WED to me and said that she agrees with all the other doctors that I have a really severe case of WED and she said she thinks I may also have fibromyalgia.
She is weaning me off the Pramipexole and getting in touch with my primary to explain to him why I need another iron infusion. She said anybody with WED needs to have a ferritin level over 75. I think mine was at 60 last time it was checked. It was at 189 after my last iron infusion which was Jan/Feb 2011. So for the next 6 weeks my drugs will be 0.5 mg of Pramipexole at 7am and 6pm. I take a 10mg Oxycodone at 6pm and can have another one during the day if I need it.
My primary had changed my antidepressant from Wellbutrin to Cymbalta about 3 weeks ago. That change made the WED worse but made so many other things better that this doctor said she wanted to keep me on the Cymbalta anyway. I have been so much more clear headed and so many of the little aches and pains in my legs and lower back are about gone since starting the Cymbalta that I really am hoping we can control the WED so I can remain on it.
I also have to go for another sleep study to see if I have sleep apnea now. She thinks I do....I guess we will find out in a few more weeks.
I go back to U of M the first part of October to see her again and she is going to adjust my meds again and hopefully I will be done with Pramipexole for good. So far the Oxycodone makes me kind of sleepy but I am not getting sick like I was on the Methadone and the Vicoden I was taking didn't seem to do much more then a Motrin did.
I will let you know how things go....right now the WED is not good but I kind of expected things to get out of control for awhile during this drug change.
Have a great day...it is muggy, hot and humid here today.
She is weaning me off the Pramipexole and getting in touch with my primary to explain to him why I need another iron infusion. She said anybody with WED needs to have a ferritin level over 75. I think mine was at 60 last time it was checked. It was at 189 after my last iron infusion which was Jan/Feb 2011. So for the next 6 weeks my drugs will be 0.5 mg of Pramipexole at 7am and 6pm. I take a 10mg Oxycodone at 6pm and can have another one during the day if I need it.
My primary had changed my antidepressant from Wellbutrin to Cymbalta about 3 weeks ago. That change made the WED worse but made so many other things better that this doctor said she wanted to keep me on the Cymbalta anyway. I have been so much more clear headed and so many of the little aches and pains in my legs and lower back are about gone since starting the Cymbalta that I really am hoping we can control the WED so I can remain on it.
I also have to go for another sleep study to see if I have sleep apnea now. She thinks I do....I guess we will find out in a few more weeks.
I go back to U of M the first part of October to see her again and she is going to adjust my meds again and hopefully I will be done with Pramipexole for good. So far the Oxycodone makes me kind of sleepy but I am not getting sick like I was on the Methadone and the Vicoden I was taking didn't seem to do much more then a Motrin did.
I will let you know how things go....right now the WED is not good but I kind of expected things to get out of control for awhile during this drug change.
Have a great day...it is muggy, hot and humid here today.