What tremor would you call mine?

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clinnychiggy
Posts: 2
Joined: Fri Dec 31, 2004 6:48 pm
Location: New Jersey U.S .A
Contact:

What tremor would you call mine?

Post by clinnychiggy »

My case might not be orthostatic but I have a body tremor.It is basically noticeable with my hands when I engaged in something.I realised it when I was 11, and it affects me a lot socially that I get depressed cause it.

My memory is not as good as it used to be.I get easily exhausted.Sudden rise in my heartbeat as if I am anxious about something when I'm not. My palms tend to coldsweat.

I feel more relaxed in the evening times but the tremor is still there.

I've seeked medical attention but not much attention was given.

I write to see if anyone could proffer any help or assistance.

I'm 18 years old by the way.
Lynda
Posts: 42
Joined: Sun Jan 25, 2004 10:37 am
Location: West Sussex, UK

Type of tremor

Post by Lynda »

Hi!
I'm so sorry to hear about your tremor. I think we can all identify with the anxiety and depression that a tremor can cause, especially in social situations. The symptoms of a rapid heartbeat and sweaty palms sound very similar to the anxiety and panic attacks that I experienced before I discovered that there was a name for my condition - and that it wasn't 'all in the mind'! Things changed a lot after finding a diagnosis (through this website) and finding the support of others suffering in the same way - and so I think it's very important that you discover exactly what your tremor is and that you find some support. Obviously you've been taking steps to do exactly that.
It's dangerous to make a diagnosis over the internet - not knowing you, and having so little medical info - but it sounds to me as if you could be suffering from Essential Tremor. Please don't take my word for it, but do some more searching for yourself. There are plenty of websites that you could investigate further eg http://www.essentialtremor.org, http://www.wemove.org and http://www.tremor.org.uk. The last one is a British organization which deals primarily with essential tremor and has a message board like this one. It also has a list of types of tremor, which may help you.
I do hope you are successful in your quest. Don't give up - and keep smiling!
Lynda
gloria
Posts: 826
Joined: Sun Jan 18, 2004 1:10 pm
Location: New Jersey, USA

Post by gloria »

Lynda, you posted a very good reply to "Clinnychiggy" and I would like to add a bit more information. "Clinnychiggy" I noticed that you are from New Jersey which is my home State too. Since we both live near New York City I have a suggestion as to where you might be able to find a neurologist that can give you a diagnosis for your tremor and that would be:

NY Columbia University Neurological Institute
710 West 168th St.
New York, NY 10032
Tel. 212-305-3665

Good luck and please stay in touch, Gloria
clinnychiggy
Posts: 2
Joined: Fri Dec 31, 2004 6:48 pm
Location: New Jersey U.S .A
Contact:

Thanks alot!!

Post by clinnychiggy »

thanks Gloria and Lynda...I rlly appreciate ur assistance
Betty
Posts: 391
Joined: Thu Jan 22, 2004 3:08 pm
Location: Melbourne, FL

Your Tremors

Post by Betty »

Hi Clinnychiggy!

I haven't been on the site for a few weeks, and am trying to catch up with all the new postings. I found yours interesting and especially the one from Gloria.

If there is ANY possibility of going to Columbia Presbyterian Medical Center in New York ~ GO!!!

I went December of 2003 and got a definitive diagnosis through testing. It has taken me years to find out I have OT and it was such a relief to finally know. I was seen by Dr. Seth Pullman; he is wonderful.

I know there are many other neurologists there, but he was the one I saw. Do take Gloria's advice and check it out! You won't be sorry.

Betty
porotin
Posts: 28
Joined: Sat Jul 17, 2004 7:59 am
Location: Sydney,Australia

Re: Your Tremors

Post by porotin »

Betty wrote:Hi Clinnychiggy!

I haven't been on the site for a few weeks, and am trying to catch up with all the new postings. I found yours interesting and especially the one from Gloria.

If there is ANY possibility of going to Columbia Presbyterian Medical Center in New York ~ GO!!!

I went December of 2003 and got a definitive diagnosis through testing. It has taken me years to find out I have OT and it was such a relief to finally know. I was seen by Dr. Seth Pullman; he is wonderful.

I know there are many other neurologists there, but he was the one I saw. Do take Gloria's advice and check it out! You won't be sorry.
Hello Betty:
I havenot been able to came to the forum like i will like it!! but thinking in all of you in this past week's but I have een very sad with the tragedy in Indonesia ,work and my son that he is also disable.Love from Porotin
To the new menber yes get to see a Dr who can tell you what is it?? is very importantfor you!! take care Porotin

Betty
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