Poughkeepsie Paranormal Investigators

05/03/2023

If everyone could, my nephew did this song in it's entirety about the reality of the drug pandemic fentanyl. Please take a listen....

In this Reason 12 music production challenge, I asked my friends and family to write down random songs or sounds for me to create. At random I pick them out ...

04/23/2022

https://www.facebook.com/112140506930163/posts/545882733555936/

Hello, my name is James, I've created this fund raiser for my son James Jr. Who is 13 year… James Mulcahy needs your support for Donate to help for James Jr.

04/01/2020

Hello everyone, please help my son james by voting for him, here is a link just scroll down to his picture, click his picture and fill out info! You can vote up to 5 times!!! Per day per email. This is his picture....

https://hvparent.com/forms/default.aspx?id=359

02/29/2020

https://www.poughkeepsiejournal.com/story/news/local/2020/02/28/gm-1-gangliosidosis-rare-disease-poughkeepsie-family/4859745002/

In honor of rare disease day this Saturday, we decide to share a more intimate moment of our sons life's journey dealing with GM1 GANGLIOSIDOSIS

A City of Poughkeepsie couple is struggling to find answers for their 11-year-old son's rare genetic disease.

02/28/2020

https://m.facebook.com/story.php?story_fbid=145206360290244&id=112140506930163

02/22/2020

Due to personal life issues, we have not taking on any new cases nor have we hosted any lectures/events. For the time being it's going to remain this way for a little bit, however it isn't the end. We are still very active as a team and group and will continue to help those who come to us. We appreciate all our fans and followers for sticking with us through out the years and especially as of late due to our inactivity. Right now personal life comes first. Thanks for the understanding and continued support of our team.

01/14/2020

Where's all our para peeps at? Let's get the word out about this devastating disease....smash the like button then share the page. Let's raise awareness together!

On November 7th, 2019, our son James was diagnosed with a vary rare and fatal inherited neurodegenerative genetic disease called GM1 Gangliosidosis Type 2 Juvenile. This is our story.

01/09/2020

Let's get the word out there, let's all raise awareness, hit that like button and share it!

On November 7th, 2019, our son James was diagnosed with a vary rare and fatal inherited neurodegenerative genetic disease called GM1 Gangliosidosis Type 2 Juvenile. This is our story.

01/09/2020

Hello para peeps, if you would please stop by my son's page, smash the like button share the heck out of it and let's find a cure for this nasty genetic disease! Please and thank. Also keep the prayers coming we definitely appreciate it.

https://www.facebook.com/hopeforjimjim/

On November 7th, 2019, our son James was diagnosed with a vary rare and fatal inherited neurodegenerative genetic disease called GM1 Gangliosidosis Type 2 Juvenile. This is our story.

01/03/2020

Happy New year everyone. Here's some food for thought!

12/19/2019

Hello all, if you all wouldn't mind, please smash the like button on the link below! Also please share it! Together and with your help, we can spread awareness about this rare and fatal disease. Thank you all so very much.
https://www.facebook.com/hopeforjimjim/

On November 7th, 2019, our son James was diagnosed with a vary rare and fatal inherited neurodegenerative genetic disease called GM1 Gangliosidosis Type 2 Juvenile. This is our story.