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progressive supranuclear palsy | PSP | fightpsp.com Reviews
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Stem Cells | progressive supranuclear palsy
https://fightpsp.com/2011/12/14/stem-cells
Laquo; 4 years. December 14, 2011. A few weeks back on a friday morning, my father called me full of excitement. he told me that there might be a cure for PSP. Immediately i logged in to the website that he had done his research on, basically it was a hospital located in Shanghai that specializes in Stem Cell implants, and one of their patients was a PSP patient, whom they saw some good results after the implant. It did seem to good to be true… hopefully one day, a treatment will be found. Back to the top.
August | 2013 | progressive supranuclear palsy
https://fightpsp.com/2013/08
Archives for the month of: August, 2013. August 19, 2013. PEG Tube Part II. August 5, 2013. Http:/ en.m.wikipedia.org/wiki/Percutaneous endoscopic gastrostomy. The dr mentioned that the most important note to be taken is the aftercare. We have already taken a step and will be hiring a part time nurse to be helping at home with mama. Blog at WordPress.com. Back to the top. Follow “progressive supranuclear palsy”. Get every new post delivered to your Inbox. Join 221 other followers.
About PSP | progressive supranuclear palsy
https://fightpsp.com/about
The reason i started this blog is to discuss PSP, as it a very rare brain disease that effects every 1 in 100,000 people worldwide. Unfortunately, my mother is one of those people. I will be talking about our experiences with her, and also discuss updates and different information about psp. God Bless her, she is a strong woman who is fighting psp. Or leave a trackback: Trackback URL. July 26, 2014 at 6:53 pm. It was hard to find your page in google search results. September 2, 2014 at 6:16 pm. Build a w...
4 years. | progressive supranuclear palsy
https://fightpsp.com/2011/12/13/4-years
Laquo; Back Home. . . December 13, 2011. Yesterday was my four year anniversary. and i just realized how much has happened in four years. Im happily married to the best wife in the world, I have a wonderful baby girl that is 1 year and 10 months, lots of nanny drama around the house, took numerous trips all around the world. thankfully iv’e done a lot in the last four years. Or leave a trackback: Trackback URL. December 13, 2011 at 12:05 pm. What a wonderfully thoughts written on mum. Thanks. . I...Leave...
progressive supranuclear palsy | PSP | Page 2
https://fightpsp.com/page/2
May 19, 2011. One of mama’s dr’s, a lebanese (how ironic) recommended botox as a treatment , he said it will help with the drooling, as her mouth shouldnt be as droopy, and also will relax her neck muscles and frown looking face. Yesterday she had her first botox session, and thankfully says she already feels more comfortable, especially in her neck. May 12, 2011. PSP displays a wide range of symptoms including:. Weakness of eye movements, especially in the downward direction. Http:/ www.psp.org/...PSP i...
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progressive supranuclear palsy | PSP
October 15, 2017. After a long battle with PSP, my mother has gone to a better place. She is at peace. I will update this website, more often and back track the last four years as well as I can. August 19, 2013. PEG Tube Part II. August 5, 2013. Http:/ en.m.wikipedia.org/wiki/Percutaneous endoscopic gastrostomy. The dr mentioned that the most important note to be taken is the aftercare. We have already taken a step and will be hiring a part time nurse to be helping at home with mama. July 27, 2013. And s...
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