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in reply to: Shameless Plug for the Conference #1068172
Will transcripts be available from the conference speakers? I cannot even imagine I would ever be well enough to attend one. I went undiagnosed for 3 years, and although I have been on methimizole for 3 months, my levels are still very high, and I still feel worse than terrible. It’s hard to be out of bed for more than 2 hours, I cannot even fathom going to a conference 1100 miles away, but would LOVE to read the information.
in reply to: im so tired of my mom saying… #1070523Wow, Hopeful, sounds like we could have the same mother! I also have a sister who is a constant discouragement. "Just get off your butt and get a job, and that’ll make you feel better!" "When you have a symptom that I haven’t had yet, then I’ll listen to you!" "I have to get up and work everyday, even when I feel bad, and you don’t see me complaining."
After awhile if all sounds like "Blah Blah Blah Blah…" I was diagnosed in April, after 18 months of symptoms, and still am not being treated (other than beta blocker and diuretic). It is 5 weeks until my endo appointment. My muscles are totally gone. I can’t even carry in groceries, but my 14 year old helps. I had to go the ER last week for an anaphylactic reaction to something, they don’t know what, but said they thought the hyperthyroidism played a part. Their remedy was to take Benadryl every 4-6 hours for the next 5 weeks until my appointment. And of course, my family thinks I overreacted. My throat was almost swollen shut, I started violently vomiting, My pulse was 200, but of course, I was making a big deal out of nothing….. It is so frustrating! I had to drive myself the 15 miles to the hospital! And my family is educated on medical things, my sister is a nurse practicioner, my dad was a doctor, I am an RN.
So I really comiserate with you on the family thing! I do not live with my mother, but live 1 mile from her in a house that she owns, and pays utilities on. I have worked to develop a support system outside my family, through church and a Celebrate Recovery group, so I do have others to turn to, however, no one else suffering with Graves. I have really appreciated the information gained from this board, and have learned so much. I am proud to be a part of this community.
Hang in there Hopeful, I know how you feel, and just know it will not last forever. I believe you are well on your way. I look forward to beginning my own treatment, and learning from your experience.
This is such excellent information that I needed to know. Thanks so much for sharing it. I feel I have so much to learn about what is going on with me, it is discouraging. I have only had my diagnosis for a week and a half, and feel like I’ve been hit with a truck physically, and emotionally from trying to learn how to best take care of myself. I miss my old self before I got sick.
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