Acquiring out about getting an auto-immune sickness was a little something I was in no way ready to communicate about until eventually now. I hope my tips allows.
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Hi Hitgirl x Bex! Hope you are going great! I was just wondering how long it took until you were able to start exercising. I completely understand about the psychological issues that can occur. Currently I am almost a year into treatment and still can't exercise.
Sorry but I totally got distracted by that poster behind you. Schematics and blueprints pique my interests a lot lol. Nice video though, good for you for staying so positive. Wish you the best!
Hi, Has Graves disease affected your sex drive in anyway.
Pretty girl, great video
yesssssss I got through it all the time. people don't understand y I'm Moody or very tired,
but I can't explain it but I already have a autoimmune disease colitis. well I'm glad to see someone else. feels this way
did your eyes get bigger with this disease
did your eyes get bigger with this disease
Thanks so much Bex just found out yesterday about me having graves disease. Im glad to hear a positive .
Hello thanks for sharing, i was diagnosed with Graves 3 years ago, never put on any meds yet because my endo said my levels are still in norma range, my heart rate is normal, just some times i'll get heart fluttering and sometimes i'll feel out of breath but mainly when I try climbing stairs or hills, do you get those symptoms?
there is a link between graves and celiac… have you looked this up?
Thank you for this video. I was just diagnosed with Graves' disease yesterday and I'm very confused and lost. Your video helped me tremendously.
How are you feeling today?
Thank you for sharing your video, and for having such a positive outlook on life 🙂
Not all doctors have the same backgrounds, and so treat diseases using different methods. I would definitely research, then get a second opinion, as autoimmune disorders can be treatable through diet. This includes Graves disease. If you remedy yourself this way, rather than medication, it may help reduce risk of cancer, as the actual inflammation itself should resolve if you eliminate it's source. (There could be many sources, but food is a big one)
I have this same issue. just that I got my thryoid removed I now take synthroid, but I like how you said that the levels fluctuate I was having that issue myself and see that you are experiencing the same thing as me with the constant blood tests. I love your anology and I feel a lot more confident because of this video. thank you very much
How are you doing today? I just got diagnosed with hyperthyroidism they put me on Metoprolol, your heart was beating faster than me scary!, I just usually get the shakes, hope I can beat this stupid thing :(
Nice video, thank you.
I was diagnosed with graves disease today and watching this really helped. I'm 18 and as long as I remember I've had symptoms. It was quite comforting to know that I'm not alone.
you're awesome. you sound so positive. I was diagnosed with graves disease lastyr feb 2015. symptoms leading up to my diagnosis were unusual muscle pain mainly in the evening/early morning, eating more/drinking less, unusual bowel movements, weight loss and my hair line was a bit off. hair is also dry at times and the strands are very very thin. I just wanna know if you or anyone out there is experiencing the hair problems that im facing. everything else is ok its just that my hairline is still the same and just wondering if it will grow back. I know there are people out there who have it worse than i do but i just want to know if once the t3 and t4 levels are normal will the hair thats shed return?? im currently on 200mcg levothyroxine and have started taking Evening Primrose Oil supplements as I've heard this can help the hair grow. Thanks! God bless yall
you're awesome! I had a bad virus that left me really sick.Im still on the road to recovery,this video really encouraged me to keep pushing.Love your positivity ♡
I've had a thyroid problem for about four years now, I was originally hyper, but I took the iodine radiation pill which killed my thyroid off, so I have been taking levothyroxine for the last 3 years, it was what seemed like a long process, I went from my thyroid numbers being 47 to almost normal which is .3 or .4, but just recently I was acting hyper, nervousness, anxiety Attacks, fast pulse rate, so I decided to go to the doctors, when my thyroid test came back it pretty much said that my thyroid was overactive once again from the medicine dose being to high (I took .250 mg's in the morning) so now I'm waiting to see my Dr, so I can lower my dose 🙂 thyroids are crazy!
Bex_HitGirl, I just wanted to say thank you. Thank you for sharing this vid. A very dear friend was just diagnosed with Graves this year and we are separated by almost 1300miles, so I am unable to be there for her like I would like to be. Just once again and most sincerely thank you for sharing.
I agree that the psychological aspect of Graves' Disease is one of the hardest parts.