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Chloe shares her experience of living with essential tremor 

National Tremor Foundation
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Chloe shares her experience with essential tremor, at the NTF Essential Tremor Open Day March 2018 in Oxford.
If you would like to share your video of your experience with tremor email enquiries@tremor.org.uk
The National Tremor Foundation is an organisation where we aim to provide help, support and advice to all those living with all forms of tremor irrespective of age. For more information go to www.tremor.org.uk

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29 июн 2024

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Комментарии : 18   
@chrisharris1705
@chrisharris1705 2 года назад
hi im Chris I've had essential tremors since I was 6 years old I'm now 39 you give hope and encouragement to all of us thank you
@laurenrootham7868
@laurenrootham7868 6 лет назад
Hey, Chloe! I don't know if you remember me from some of your German classes at Uni, but hope you're well! Just wanted to say that I think it's fab that you're speaking out and talking more about your essential tremor and I have a lot of admiration for that! Keep doing what you're doing, and don't let it stop you from achieving all you dreams and wishes! Und ich hoffe auch, dass deine Zeit in Deutschland Spaß gemacht hat! Take care, girl! :) P.S. And if it's any consolation, I barely even noticed your tremor!
@lindahe8195
@lindahe8195 6 лет назад
Lauren Rootham How did you treat the tremor?
@TheHansBeekhuyzenChannel
@TheHansBeekhuyzenChannel 2 года назад
I had ET since my 20th. At 66 it got so worse that drinking from a cup or glass was extremely difficult since my hands were shaking severely. I also developed a head tremor over the years. I tried six types of medication but they didn't solve the problem. So in 2021 I underwent the DBS operation. I explained why in a video. Two weeks after the operation I made another video. The videos are not sponsored in any way.
@TamiePryor
@TamiePryor 2 года назад
I noticed that my son starting having them in middle school. We were told that they are hereditary but we do not know of anyone in the family who has them. Does anyone in Chloe's family have them?
@gowthami7701
@gowthami7701 2 года назад
Even I have tremors since my childhood
@dhandekrushna4055
@dhandekrushna4055 2 года назад
Are you from India?
@gowthami7701
@gowthami7701 2 года назад
@@dhandekrushna4055 yes brother
@dhandekrushna4055
@dhandekrushna4055 2 года назад
@@gowthami7701 aapne treatment nahi liya ?
@dhandekrushna4055
@dhandekrushna4055 2 года назад
Mujhe bhi ET hai jab mai 18 complete hua tab se yeh badh Raha hai
@gowthami7701
@gowthami7701 2 года назад
@@dhandekrushna4055 iam taking propranolol & no more treatment
@maryjones8726
@maryjones8726 2 года назад
Get tested for a vitamin B12 deficiency.
@KishBish
@KishBish 2 года назад
I have tremor and my B12 was elevated..
@maryjones8726
@maryjones8726 2 года назад
@@KishBish Sally Pacholok in her book "Could it be B12?" states that there is much controversy as to what constitutes a normal result for B12. She believes the "normal" serum B12 threshold needs to be raised from 200 pg/ml to at least 450 pg/ml.
@KishBish
@KishBish 2 года назад
@@maryjones8726 mine is 1824 pg/mL lol.. I know bc I recently had labs and specifically requested my B12, magnesium, and D3 numbers.. I supplement over what is suggested, so I keep an eye on things.. I'm not really sure what is causing the tremor, but I've had it since I was a teen (I'm 46) and the only thing that ever completely stops it is Klonopin, but I haven't taken that in years.. could be my dental amalgams, who knows..
@colefox2882
@colefox2882 Год назад
Ah “B12 deficiency” . . Every ET, PD, MS & ALS patient’s dream. 🙃
@HBD777
@HBD777 3 месяца назад
@@colefox2882wanted to say this lol. People who don’t have it totally get that it’s probably just b12. All the tests and seizures point right to the vitamins 😂
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