FOR GREGORY

Periodically I will add posts here if the sources provide additioanl informaiton on how to think about and deal with Dementia/ Alzheimer's Disease.

PLEASE NOTE:


SCROLL DOWN FOR TEXT and BIBLIOGRAPHY from DAI WEBINAR 2/22-23/2017. You can also find this information on my website: www.horvich.com


Even though this blog is now dormant (see info below) there are many useful, insightful posts. Scroll back from the end or forward from the beginning. My guess is that you could spend a lot of time here and maybe learn or experience a thing or two about living with and loving someone with Dementia/Alzheimer's or maybe come away with the feeling that "you are not alone" in YOUR work with the same!


• • • • •


THIS WAS THE FINAL POST TO THIS SITE BEFORE IT WENT DORMANT.


Happy New Year 2016. With a new year comes new beginnings and sometimes endings. If I am personally progressing and if I am doing a good job in my grieving Gregory's death; if I have been able to learn my lessons in living and loving someone diagnosed with Dementia/ Alzheimer's; if I am to get on with my life ... I need to bring this Alzheimer's blog to an end since my writing has been dealing less with Dementia/ Alzheimer's and more with life after Dementia/ Alzheimer's.


Of course, I will always continue to work for and support fair treatment on behalf of people with Dementia/ Alzheimer's and may post here from time to time. Also, there are many wonderful posts here through which you may browse.


With this change, I will continue and reinvigorate my "michael a. horvich writes" blog which deals with grieving Gregory's death, life lessons, personal experiences, observations, memoirs, dreams, and humor in essay and poetry, as well as an attempt now and then at sharing a piece of fiction.


Please follow me there by clicking http://mhorvich.blogspot.com or click the link located on the right side of this page.


Finally, COMMENTS are always important to me and you can still comment on the posts on this blog! CLICK "Comments" and sign in or use "Anonymous." Leave your name or initials if you wish so I'll know it's you? Check the "Notify Me" box to see my reply to you.



Monday, November 2, 2015

Call for Study Participants

I received this call for study participants from an organization who came across this blog. Their site looks good and their research intentions appear to be on the "up and up." However, I am not recommending or referring anyone based on my first hand experience with them and take no responsibility posting this. As in any situation, careful study and asking questions is your guide to making good decisions.
Fondly, Michael

 Hi Michael,

I came across your blog and its dedication to Alzheimer’s disease.  (AD) 

My partner and I own a clinical research facility on the corner of Foster and Ashland.   We’ve been open over a year, though our staff has many years of experience.  

We’re currently conducting several Alzheimer’s trials and have several more in our pipeline.  Two current trials are for those already with mild to moderate AD and a third (opening soon!) is an AD prevention trial called A4.

A4 is sponsored the the National Institute of Health (NIH).  This trial is for those 65 and over who are healthy and not showing signs of AD.  PET scans and MRI’s are used to see if those screening have the signs of AD in their brains (plaque/Amyloid/tangles), though not yet showing signs of the disease.  An investigational medication is being used to see if AD can be stopped before it becomes symptomatic.   

All three trials that we’re doing are designed to stop, slow down or prevent AD from happening.  Instead of treating only symptoms, these are “disease altering investigational medications.”  There’s NOTHING on the market now that attempts to do that.  If I had AD, I’d enter a clinical trial because there is nothing to stop it from progressing and by entering a clinical trial, I might be able to benefit from it, but for sure, others will too.

We are having a very hard time recruiting volunteers for our trials.  We don’t know why, but we need a number of people who have AD already for us to continue this valuable research in the hopes of finding a cure.   

Is there anyway you can help us get the word out?  It seems like such a waste that this option is available to people with AD, though few are taking advantage of it.

Thanks for you time reading this.   D



Dean Hervochon, Executive Vice President
Great Lakes Clinical Trials
5149 North Ashland Avenue
Chicago, IL 60640 USA
Mobile:  (773) 454-1312
Phone:  (773) 275-3500
Fax: (773) 275-3501
Email: dhervochon@greatlakesclinicaltrials.com

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