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.

Friday, June 17, 2011

Nanotechnology in Medicine - Nanomedicine

From reading the possibilities of nanotechnology in medicine, there are vast possibilities in stroke rehab, if only someone with enough foresight would look at them
The Ideal Gene Delivery Vector: Chromallocytes, Cell Repair Nanorobots for Chromosome Repair Therapy
The ultimate goal of nanomedicine is to perform nanorobotic therapeutic procedures on specified individual cells comprising the human body. This paper reports the first theoretical scaling analysis and mission design for a cell repair nanorobot. One conceptually simple form of basic cell repair is chromosome replacement therapy (CRT), in which the entire chromatin content of
the nucleus in a living cell is extracted and promptly replaced with a new set of prefabricated chromosomes which have been artificially manufactured as defect-free copies of the originals.
The chromallocyte is a hypothetical mobile cell-repair nanorobot capable of limited vascular surface travel into the capillary bed of the targeted tissue or organ, followed by extravasation, histonatation, cytopenetration, and complete chromatin replacement in the nucleus of one target cell, and ending with a return to the bloodstream and subsequent extraction of the device from the body, completing the CRT mission. A single lozenge-shaped 69 micron3 chromallocyte measures
4.18 microns and 3.28 microns along cross-sectional diameters and 5.05 microns in length, typically consuming 50-200 pW in normal operation and a maximum of 1000 pW in brief bursts during outmessaging, the most energy -intensive task. Treatment of an entire large human organ such as a liver, involving CRT on all 250 billion multinucleate hepatic tissue cells, might require the localized infusion of a ~1 terabot (trillion device) ~69 cm3 chromallocyte dose in a 1-liter 7%
saline suspension during a ~7 hour course of therapy. Chromallocytes would be the ideal delivery vector for gene therapy.

and more here;
Aluminosilicate nanoparticles can more quickly reduce bleeding in trauma patients by absorbing water, causing blood in a wound to clot quickly. Hey, possibilities for bleeders?
http://www.understandingnano.com/medicine.html

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