Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Thursday, November 5, 2015

Oestrogen Drug May Not Benefit Women With Alzheimer’s Dementia

But the real question needing an answer; Would this drug help memory and thinking skills post-stroke?
http://dgnews.docguide.com/oestrogen-drug-may-not-benefit-women-alzheimer-s-dementia?
An oestrogen-like drug, raloxifene, has no demonstrated benefit on memory and thinking skills for women with dementia due to Alzheimer’s disease, according to a study published in the November 4, 2015, online issue of the journal Neurology.
“Drugs that interact with oestrogen receptors have attracted a great deal of interest as a potential treatment for women with dementia due to Alzheimer’s disease, but relatively small studies of oestrogen have generally failed to confirm any benefit,” said Victor Henderson, MD, Stanford University, Stanford, California. “Prior to this study, raloxifene had not been evaluated as an Alzheimer treatment.”
For the study, 42 women with mild to moderate dementia due to Alzheimer’s disease were separated into 2 groups and given raloxifene or placebo for 12 months. The women were assessed on their memory and other mental functions at the start of the trial and then every 3 months. They were also evaluated on how well they could complete daily activities, and their family members or caregivers were asked about their caregiver burden and stress at the start, middle, and end of the study.
The results on the cognitive skills tests did not differ significantly between the placebo group and the group taking raloxifene. There were also no significant differences reported by family members and caregivers on the amount of caregiver burden or stress or in daily activities.
Dr. Henderson noted that the study was not designed to detect small effects from raloxifene in the range of that provided by approved Alzheimer’s drugs such as donepezil or memantine.
“We found that the drug did not have any significant effect on patients after 1 year,” said Dr. Henderson. “If there are cognitive effects in this population, these effects are likely to be no more than small. These results may be valuable if future trials of raloxifene are considered.”
SOURCE: American Academy of Neurology

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