Thank you for sharing. You are not alone. I feel like this from the waist down some days and walk strongly at times. Gentle, loving hugs! Keep going sweetie!
@davidpowell51786 жыл бұрын
Your and amazing women hang in there. I too was diagnosed with Cerebellum ataxia at 57 years old 8, months ago, I’m still learning and finding things out to slow this horrible thing out that’s taking the easy things away from me like biking, running, basketball, hiking. I hope a cure comes sooner then later,😢
@alz123alz5 жыл бұрын
MASSAGING SCALP HELPS STIMULATE NEURONS, OR BRAIN CELLS
@dicknoel112 жыл бұрын
Suzy contracted Legionnaires Disease in 2007 and has had 5 years of various therapies. She has had "regular" PT for the full 5 years and also Feldenkrais movement therapy for 5 years. She also uses a therapy pool (can walk in 4 foot section alone) once a week and therapeutic horse back riding once a week.
@misslibrus8799 жыл бұрын
Suzette you're soo amazing & such a strong lady.. i'm a patient of cerebellar ataxia too.. hugs & kisses from Malaysia!
@herpsenderpsen10 жыл бұрын
This is very fascinating, my thoughts goes to this amazing human being which shows plenty of life energy :D
@phixi0n3 жыл бұрын
My mother had seven brothers and sisters, 3 of her brothers and 1 of her sisters had/have cerebellum ataxia. When her brothers first started showing symptoms, the neighbours thought they were drunk due to the way they walked.
@MealyMouthedLeach7 жыл бұрын
Thank you for posting. Good Luck to you ! Sincerely. d.
@rastus8112 жыл бұрын
Thanks for posting this. As a PT student, I find videos like this really helpful. Do you mind telling us how much rehab has Suzette had at this point?
@junmarkreynob94442 жыл бұрын
Our baby at 2 years old is diagnosed of Cerebellar Ataxia. We found it very difficult to do the therapy considering his age. He used to be a very happy and energetic kid. Hope you can help us in his condition. A little advise and prayers will do.
@semangatsembiring98539 жыл бұрын
Yes ... you not alone mee to. Keep hope miracle comes true....
@rodrigogomes70342 жыл бұрын
Como foi a recuperação? E como está hoje?
@georgekafantaris78078 жыл бұрын
how old is patient
@davidkellar67326 жыл бұрын
Good for u
@rvc65069 жыл бұрын
Why are they called walkers? They roll.
@georgekafantaris78078 жыл бұрын
+roy childs you walk after you roll
@walterlee56883 жыл бұрын
I have the same but I have a wheelchair I'm 32
@saif1980saif6 жыл бұрын
My mom has ataxia similar to this lady and its vvv dangerous what your doing and this walker is inappropriate for this sufferer
@abeeramr62664 жыл бұрын
Hello Said , what is the correct type of walkers for ataxia patients cuz my mom is diagnosed with the same??
@saif1980saif4 жыл бұрын
@@abeeramr6266 there is no such walker. A house with hand rails is best. There is no way on earth this lady can walk independantly. Further to this, they lady assisting can in no way save her from falling if she lost total balance.
@abeeramr62664 жыл бұрын
@@saif1980saif I am trying to let her independly go to bathroom and to the other side of her room without help using the standard walker but she's always complaining and afraid to fall :(
@saif1980saif4 жыл бұрын
@@abeeramr6266 ive kept a island with rails. Give me your watsapp ill send you pics. Islands and rails is their only option. They cant coordinate frames
@abeeramr62664 жыл бұрын
@@saif1980saif please send me on +201003612705
@samironghosh57284 жыл бұрын
I think homeopathic treatment can help to treat ATAXIA
@tonypae61514 жыл бұрын
Apkk kuch fayda hua h
@samironghosh57284 жыл бұрын
@@tonypae6151 hai ho Raha hai
@tonypae61514 жыл бұрын
Aap konsi dwai use kr re ho homeopathy m name btao plzz
@samironghosh57284 жыл бұрын
@@tonypae6151 Kya apka family ma kisiko ATAXIA hai?
@tonypae61514 жыл бұрын
@@samironghosh5728 meri mother ko apna no de ya is no p contact kre 8700239896 plzwhats app no 9560917202 plz rply
@Ruth_T3 жыл бұрын
Does this come and go or is this constant?
@dicknoel13 жыл бұрын
The ataxia is constant for past 13 years after she contracted Legionaires Disease (permanent after effects---only happens to 3 % of people who get Legionaires Disease