Not asking for medical advice
Hello ladies,
I was diagnosed with Graves disease 4 years ago (won’t add more as I don’t want to make this medical). I have been trying to describe to my husband what it feels like day to day, to live with this disease. I am in my late thirties with two young kids and I feel I just can’t keep up some days.
Would you be able to describe your experiences, just so I have a greater pool of information for him to help him understand.
He has been AMAZINGLY supportive. There have been some outside stressors, which has increased the stress on him, so he has been a little more frustrated lately.
Thank you!
Comments
There’s r/gravesdisease if you haven’t visited yet.