Tags:
Replies are closed for this discussion.
Hello Becky
I don't show temours (yet) and can still eat and drink, although it takes a lot of effort. I can't write, thank goodness for credit cards and PIN's!. I am lucky in that I still have my Husband and because everything to do with money is joint he can sign and no-one is any the wiser. He covers for me a lot.
I have taken out Power of Attorney for all my affairs and I have been quite specfic. I have two attorneys, my Husband and A/N other, they can act independantly or together. I have taken out one for my affairs' and one for 'health and welfare'. It is very good I can use it whenever I want to but the attorneys cannot impose anything while I stilll have my marbles!!! Even when I have 'lost' it they have to do what I have said. I have peace of mind and that counts for a lot, everything is on a legal footing.
Let's face it this condition is enough to think about!!!
Kati one of our Community Managers has weighted wrist bands, there is a thought. They might help you. I am sure Kati will respond and when she does you can rest assured it will be sound, sensible advice.
Regards and look after yourself
Carol
Hi Becky, I have information about stopping the tremors! I was researching Ataxia as I am interviewing a friend of mine who is living with Ataxia. I'm doing a featured article on him. He just told me about his tremors stopping! I felt compelled to pass this information on to you...I'm new with this method of communication...I don't know how to get this message through to you. I hope it makes it to you. To contact me my e-mail is adkaper@live.com and my phone number is 724-747-1655. I'll be happy to send you the article...or give you his contact information so you can chat with him. Best to you, Adrienne Kaper from Washington, PA
hi becky,
i have some tremors. i could barely walk with liquids. i know its hard to get help. i dont qualify for ccoupons and i have a daughter. i manage with ss and credit cards, but there is really no help. i have a bs in computer science and been working since i was 14. i stop working a year and a half ago and i feel the need to keep working. i moved to florida and cant even get a license to drive so even if i could of work i wouldnt be able to. i tried to get a doctor so i could start a new process to get it, but i dont have insurance and private insurance rejected me. atleast my daughter has medicaid so thats a relief. thinks r tough and we just have to keep trying. exercise a lot and eat right. ur young just move a lot. i know that we feel like not getting up, but do. do a lot of things that involve hand movement.
take care of ur self
hi nati, i am so touched by ur story.it makes it harder for me because i am only 25 so i wondewr what kind of a future i will have.yes we need to take care of our general health too and i am now trying to eat healthier too.i really wish we could all meet and share stories, ataxia makes one feel so alone.take care too, becky.
nati cepeda said:hi becky,
i have some tremors. i could barely walk with liquids. i know its hard to get help. i dont qualify for ccoupons and i have a daughter. i manage with ss and credit cards, but there is really no help. i have a bs in computer science and been working since i was 14. i stop working a year and a half ago and i feel the need to keep working. i moved to florida and cant even get a license to drive so even if i could of work i wouldnt be able to. i tried to get a doctor so i could start a new process to get it, but i dont have insurance and private insurance rejected me. atleast my daughter has medicaid so thats a relief. thinks r tough and we just have to keep trying. exercise a lot and eat right. ur young just move a lot. i know that we feel like not getting up, but do. do a lot of things that involve hand movement.
take care of ur self
Hi adrienne maybe you could share with the rest of this forum about this miracle that completely stops tremors?
I would like to see a link to this product and evidence that it does what it says it does. The managers of this site will not tolerate people trying to sell products to our members under the guise of a cure for Ataxia or Ataxia symptoms. Please send proof of your claims to katilea@live.co.uk so they can be checked out.
Perhaps your friend could join himself and tell us what worked for him.
To LWA members: we would encourage you to be wary of people offering to cure you, as from my past experience the so called cures are claimed to cure many other acute or progressive conditions also! Please be cautious before paying out for these products.
This community is part of the Ben's Friends network of patient communities. Learn more at bensfriends.org.
Patient Communities
Acute Disseminated Encephalomyelitis (ADEM)
ADHD/ADD
Adrenoleukodystrophy (ALD)
Arteriovenous Malformation (AVM)
Ataxia (International)
Ataxia (U.S.A.)
Atrial Septal Defect
Autism
Brain Aneurysms
Charcot Marie Tooth (CMT)
Chiari Malformation
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Crohn's Disease
Disabilities
Eagle Syndrome
Erythromelalgia
Fabry
Fibromyalgia
Glossopharyngeal Neuralgia(GPN)
Hepatitis C
Lupus
Multiple Myeloma
Myositis
Primary Sclerosing Cholangitis (PSC)
Psoriatic Arthritis (PsA)
Synovial Sarcoma
Trigeminal Neuralgia (TN)
Von Willebrand's Disease (VWD)
Other Rare Diseases
© 2012 Created by Ben Munoz.