1. Registering for the Forum

    We require a human profile pic upon registration on this forum.

    After registration is submitted, you will receive a confirmation email, which should contain a link to confirm your intent to register for the forum. At this point, you will not yet be registered on the forum.

    Our Support staff will manually approve your account within 24 hours, and you will get a notification. This is to prevent the many spam account signups which we receive on a daily basis.

    If you have any problems completing this registration, please email support@jackkruse.com and we will assist you.

Lisa Mancin
Last Activity:
Feb 12, 2019
Joined:
Nov 2, 2018
Messages:
2
Likes Received:
1
Trophy Points:
0

Following 1

Gender:
Female
Birthday:
June 7
Location:
Platte City, MO
Occupation:
Registered Dietitian

Share This Page

Lisa Mancin

Gold, Female, from Platte City, MO

Lisa Mancin was last seen:
Feb 12, 2019
    1. There are no messages on Lisa Mancin's profile yet.
  • Loading...
  • Loading...
  • About

    Gender:
    Female
    Birthday:
    June 7
    Location:
    Platte City, MO
    Occupation:
    Registered Dietitian
    Hello! I am a 57 year old, happily married mother of three. I am a Dietitian and my husband is a Dentist. Our oldest son is 32 y.o. and he is also a Dentist. My middle son is 21 y.o. and he suffers with Duchenne Muscular Dystrophy. I also have an adopted 13 y.o. daughter who struggles with her weight. Although my husband and I have both worked in a healthcare setting for over 30 years we are not traditional healthcare providers. I am ashamed of what both the dental field and dietetic fields have become. When our son was diagnosed with Duchenne MD our world was turned upside down and we have done everything we can to prevent his decline. One of very few silver linings that I have encountered in dealing with his disease is a wealth of knowledge that I would not have had otherwise, There is no cure for MD so it forces patients and parents to look elsewhere for answers. We have scoured the web and the world for answers, but never really felt like we were getting the full picture. Although MD is a genetic disease I feel like the information I am finding through your podcasts, videos, etc are bound to improve not only his condition- but that of our whole family. I have "skin in the game" and am looking forward to learning more and more every day. There is obviously a ton of information here, but I am spending as much time as I can trying to get the full picture. I won't lie-- 5G scares the hell out of me -- so hoping to get a grip on what I can do for my family now. Thanks for all you do. Hope to meet up with you someday!