Living with the MonSter

Hi everyone,

This is your blog!!! As many of you already know, we (my wife and I) are local filmmakers working hard to spread the word about the MS cause, and we decided to it the best way we know; producing a documentary.

As its name suggest, the documentary will be about the life of the patients after they've being diagnosed; how it has affected their lives and families, about the challenges, and the enormous efforts of the caregivers, researchers, families and patients.

Many of you already know or have heard of Stuart Schlossman. Stuart is helping to produce this documentary as well as the many other hats he continues to wear, in order to provide information and to help his MS Peers.

Interviews with the patient(s), family member(s) and caregivers had begun in January 2007 and we are almost at completion of this individual interview process. However, we are still filming various group related topics including support groups and other MS related Functions. Both Spanish and English speakers are welcomed

If you and/or a family member/ a caregiver would like to be interviewed and/or participate in this documentary, please contact Stuart by email/phone to learn where we will be next.

If you have an idea for an event that you wish us to film, please contact either myself or Stuart, to discuss your thoughts. .

All phases and stages of MS are welcomed.

A waiver release needs to be signed if you are to take part in this filming. This is for both, YOUR and Our benefit.

Please take note that unfortunately not everybody will be selected to appear on the documentary as there are just too many people in South Florida effected/affected, by Multiple Sclerosis. But any help, comments and/or ideas are really appreciated.

I hope to hear from you soon. God bless you all!

BloC-O

Living with the MonSter

As many of you already know, BloC-O L.L.C. is working hard to spread the word about the MS (Multiple Sclerosis) cause, and we decided to do it the best way we know; producing a documentary.

This documentary has been in production for about 6 months now and will be about the life of the patients after they've being diagnosed; how it has affected their lives and families, about the challenges, and the enormous efforts of the caregivers, researchers, families and patients.

Welcome!!!

Hi everyone,
This is your blog!!! As many of you already know, we (my wife and I) are local filmmakers working hard to spread the word about the MS cause, and we decided to it the best way we know; producing a documentary.

As its name suggest, the documentary will be about the life of the patients after they've being diagnosed; how it has affected their lives and families, about the challenges, and the enormous efforts of the caregivers, researchers, families and patients.

If you and/or a family member/ a caregiver would like to be interviewed and/or participate on this documentary, please feel free to contact me by email/phone. Interviews can be done at your home or a local park or other facility. Both Spanish and English speakers are welcomed.

Interview appointments will begin in early January so please do respond, if you want to get involved with this much needed documentary. All phases and stages of MS are welcomed.

A waiver release needs to be signed if you are to take part in this filming. This is for both, YOUR and my benefit.

Please take note that unfortunately not everybody will be selected to appear on the documentary as there are just too many people in South Florida effected/affected, by Multiple Sclerosis. But any help, comments and/or ideas are really appreciated.

I hope to hear from you soon. God bless you all!

Amaury