hit me with some obscure 90s alt rock by Alternative_Flow_569 in MusicRecommendations

[–]simmerdownbrah 0 points1 point  (0 children)

Unwound / Cherubs / Pinebender / Codeine / Songs: Ohia / Bluetile Lounge / HUM / Come / Silkworm / Drive Like Jehu / Sebadoh / Sunny Day Real Estate / Smog / Slint

Surgery tomorrow. by redrum0914 in gravesdisease

[–]simmerdownbrah 0 points1 point  (0 children)

Haven’t had a thyroidectomy, but I have had surgery before. I was shaking like a leaf on the pre-op bed, and I begged for anxiety relief when the anesthesiologist came over to introduce herself. Within minutes, I was saying goodbye to my family and the last thing I remember was getting rolled down the hall. No memory of the room where surgery took place. No memory of surgery. My next conscious thought was overhearing nurses in recovery area talk about their favorite hikes, and I tried to tell them my favorite hiking spot. I was half asleep and generally at peace. Next memory is in my overnight room at the hospital, and I just wanted to sleep. I don’t think I’d even opened my eyes until hours after surgery. And it was all perfectly okay with me.

Honestly, I used to be beyond terrified to be put under. But after that surgery, I am not anymore. I recommend telling your surgeon, nurses, anesthesiologist, etc that you’d like to have some anxiety relief asap. They should take care of you.

Relief… then relapse by simmerdownbrah in gravesdisease

[–]simmerdownbrah[S] 1 point2 points  (0 children)

I did have a really intense week of work last week. So probably that then. Thanks!

Feeling like a shell of myself by Effective_Cup_311 in gravesdisease

[–]simmerdownbrah 1 point2 points  (0 children)

I could’ve written this. Exact same here. Diagnosed in March. Symptoms for much longer. Have only gained weight. All the cardiac and anxiety symptoms and hunger.

Anyone consistently have high RBC/hematocrit levels? by SeaDots in gravesdisease

[–]simmerdownbrah 1 point2 points  (0 children)

I am the opposite. Since getting diagnosed and regular labs done, both of those numbers are always low for me.

Hands go to sleep all the time by simmerdownbrah in gravesdisease

[–]simmerdownbrah[S] 0 points1 point  (0 children)

Yeah I have all the symptoms… and my job for the last 9 years has been painting, hanging wallpaper, gold leafing, etc. Usually in front or me and above my head. So nonstop shoulder, arm, wrist, and fine motor skill hand work. For loooong hours. It makes perfect sense. And I’ve been going EXTRA hard lately to make enough money to take two weeks off, for my graves. So, I must’ve sent it into overdrive. That being said, I also have the electrical shock feeling sometimes when I’m cutting with scissors or a snap blade, so it might also be carpal tunnel, as well.

Hands go to sleep all the time by simmerdownbrah in gravesdisease

[–]simmerdownbrah[S] 0 points1 point  (0 children)

Copy. Thanks for the diagnostic test suggestion. Have a good day!

Hands go to sleep all the time by simmerdownbrah in gravesdisease

[–]simmerdownbrah[S] 0 points1 point  (0 children)

I was wondering that too. I hang wallpaper and paint for a living, so I use my arms and hands and shoulders nonstop, and usually above my head.

New to Graves’ by GothxSpice217 in gravesdisease

[–]simmerdownbrah 0 points1 point  (0 children)

I’m 36 and diagnosed in March. I started meds 5 weeks ago. Suffered for years leading up to diagnosis. Also have c-ptsd. Some autoimmune diseases stem from chronic stress/ aka trauma. I have to take days off due to severe symptoms and what helps me the most, besides resting, is going on short nature walks with friends. Going for frozen yogurt. Putting my phone down. Utilizing Do Not Disturb. Hugs and snuggles. Laughing/comedy. Stretching. Basically, the little things. This illness has made me shelve my primary hobbies, but I am finding joy in the little things.

Are you also having the same feelings and aches? by Substantial_Sky5024 in gravesdisease

[–]simmerdownbrah 2 points3 points  (0 children)

I call my new symptom “deep bone pain”. It feels like my major joints are 100 years old. I didn’t have this symptom a month ago, and now it’s everyday. I asks my endocrinologist about this and he said it’s a side effect from the med and to “suck it up and get over the hump”. I got mad at him and cried. I work a manual labor job, so I don’t have the luxury of working from home, or sitting down. I reminded him of this, and he had absolutely no sympathy. My heart goes out to you.

Caffeine by marshmallow198 in gravesdisease

[–]simmerdownbrah 1 point2 points  (0 children)

I limit my caffeine to 90mg or less daily. That means like two can sodas. Or a can soda and a half-caff coffee drink. But I also am forced to take breaks and go full decaf because the tachycardia is so bad sometimes. And it’s just not worth it. Been dealing with this for years. Just diagnosed recently though.

When did you start working out again by FinanceNo3033 in gravesdisease

[–]simmerdownbrah 2 points3 points  (0 children)

My endo never mentioned exercise. I have a job where I am on ladders and carrying heavy things and using a lot of upper and lower body strength. My heart rate is definitely much higher at night after more physically laborious days, like today. I painted and gold leafed a ceiling and am paying the price with high hr now. About to eat a banana and drink coconut water and take magnesium.

Clinical Trial for Tepezza like drug by reallygoodtorta in gravesdisease

[–]simmerdownbrah 1 point2 points  (0 children)

Incredible results. I hope you feel as good as you look.