As the disease has progressed, we now need to play a bigger role in determining the type of meds, frequency of meds and dosage.
Week starting 11/11/13, she was on the following
- Syndopa, 125 mg, twice daily.
Observations:She was having very little on-time and was awake all night and needed to be helped in/out of bed and walking. There is moderate dyskinesia during the on time.
Week starting 11/18/13, we changed to
- Syndopa, 125/2 mg, four times a day, every 5 hours - 7 AM, noon, 5 PM, 10 PM.
- Pramiplex, .25 mg, two times a day - 7 AM, 10 PM.
- Neupro patch 1 mg/24 hours
Observations: The on-time starts about half an hour after giving Syndopa and lasts for about 2 to 3 hours after giving the meds. She still has trouble sleeping through the night - sleeps about 5 or 6 hours while getting up every hour or two. There is moderate
dyskinesia during the on time.
On 11/26/13, we added a third Premiplex.
- Syndopa, 125/2 mg, four times a day, every 5 hours - 7 AM, noon, 5 PM, 10 PM.
- Pramiplex, .25 mg, three times a day, every 8 hours - 7 AM, 3 PM, 10 PM.
- Neupro patch 1 mg/24 hours
Observations: Mom slept for about 7 hours only getting up to go to the restroom. The extra Premiplex might have helped. Need to see now if she is alert (not drowsy) during the day.
Potential next steps are to increase the strength of Pramiplex and also increase the strength of Neupro to 3 mg after the first 28 days (around 12/20). The last resort option would be to increase frequency/strength of Syndopa and also give another medicine that decreases the harmful effects of Sindopa. This is the last resort as Syndopa has long term side effects and causes
involuntary movements (dyskinesia). The current level of involuntary movements during the on time caused by Syndopa
is already alarming.
Here are the basics of Parkinson's drugs - http://www.webmd.com/parkinsons-disease/drug-treatments
The plan is to do a weekly family conference every Sunday and adjust the meds.