Graves Disease Support
 

Hi, My name is Julie and my husband has Graves Disease. My purpose in coming to this site was to see if I can get some advice and support on how to handle my husband's horrible anger outbursts, inability to stay employed for any length of time and his general attitude since his original onset of symptoms. Things are getting really tough. I'm hoping someone who may have experienced even some of the things that are going on in my household can maybe give me the push I need to keep going. He is on medication and it seemed to really help for a few months, but now I feel like we are right back at square one even though his doctor says his levels are finally coming down. I guess a little about me: I have a beautiful daughter with my husband, she is two. I work nights to pay the bills :) and I'm tired of walking on eggshells everyday.

Hi and Welcom to Neuro Talk,

its a great place for support, full of caring people.

Here's a link to general autoimmune diseases, Graves being one of them
http://neurotalk.psychcentral.com/forum44.html

also a link to the Caregivers suppport
http://neurotalk.psychcentral.com/forum56.html

I hope this helps, but if you need help finding your way around, please ask here or send me a message, sorry you are going through this, it must be very hard.
Kate

Hi, and welcome to NT

There's lots of friendly people here. You will find a lot of support.

I pray things become easier as you struggle with this terrible disease.

We're here for you. :grouphug:

Nice to have you!
 

Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help.

There are great number of fellow members here to assist as possible. My thoughts and prayers are with you.

Again welcome, looking forward to seeing you around.

Darlene :hug:

Thank you very much to the people who have welcomed me and given me links to websites I doubt i would have found on my own. thank you so much.:):hug: