What apart from heathy food, exercise, fa... - Cure Parkinson's

Cure Parkinson's

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What apart from heathy food, exercise, faith and positive attitude has helped slow down the progress of pd for you?

hilarypeta profile image
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hilarypeta profile image
hilarypeta
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16 Replies

That about sums it up for me! :)

Court profile image
Court

Surely, there isn't anything else. Be interesting to find what is missing.

maryalice profile image
maryalice

I don't know if this slows the progression,but it sure makes it easier. HOPE! Hope for a cure.

rch21 profile image
rch21

physical therapy, tho I guess that can be considered exercise.

hilarypeta profile image
hilarypeta in reply to rch21

What kind is best? I do exercises at home, yoga/pilates, aquarobics, walking..;bit nervous of swimming as get cramp ::havent tried cycling although I love it..I wak a lot every day.;but aam lazy with my weak hand/arm;;do some one kilo weights once a day..

Gigos offfers machine type exercise/sretching ;;what do you think?

DeParkiePoet profile image
DeParkiePoet in reply to hilarypeta

the only thing that helps me, besides what you've mentioned , is meditation. I make tapes to help me meditate, because otherwise I would just think and worry... ALso try Calcium & magnesium for your cramping....

hilarypeta profile image
hilarypeta in reply to DeParkiePoet

thanks- kinesiologist says all the supplements I take make no difference! I was taking magnesium. I mediate and count breathing on waking..or if I find it hard to sleep.

rch21 profile image
rch21 in reply to hilarypeta

I find any aerobic exercise is good - I race walk 5 x per week - typical workout is 8 to 10 k in 50min to 70 min. - I also do balancing exercises which I find to be strenuous though they would not have been in the past, active warmups, strtching afterward. I try to do weight bearing exercises 2 - 3 x per week.

jeaniegal profile image
jeaniegal

. There is conflicting evidence that Azilect and CoQ10 might slow progression of PD. I am in the study of pioglitazone, testing if it could slow progression. I take Azilect and CoQ10 in case it will help, I'll let you know 10 years!

Brooke profile image
Brooke

I am going to be starting a new therapy called LSVT. It is supposed to be very intensive 4days a week for 6 weeks. The web site is Lsvtglobal.com.. I will try to keep you all informed of my progress.

CoQ10, omega 3's and B vitamins and also D3. Through reading alot about PD I've come to find that people with this disease tend to be low in the nutrients i mentioned. I had my galbladder removed 16 years ago after my daughter was born. If you don't have a gb the the fat just runs thru your body instead of being absorbed. You have to have some fat inorder for your brain to function.(I often wondered if there was a connection) My Neurologist said it is very important to reestablish these nutrients that's why it is told to eat things high in omega3s, fish , good oils watch out for things that deplete your body. It is possible to read too much about PD. (Been there done that). I like to cook so I read about nutritional info.

DeParkiePoet profile image
DeParkiePoet in reply to

I also take those nutrients in heroic doses plus a good multi and alpha lipoic acid which is a precursor to gluthathione, niacinamide and coconut butter too...

hilarypeta profile image
hilarypeta in reply to

I take them too but kinesioilogist did muscle testing on al supplements said they were not doing anything..goo to take omega 3 though. I was told I am not absorbing vit d through food and had to have injections of it. Also have fatty liver with small biliaric cysts so feel I dont absorb fats either..

PatV profile image
PatV

Yup. I can't take supplements any more. I don't absorb them. So I eat lots of fruit and veggies. People tell me I look good. Even when I feel like s***! That's what counts, right? :D

hilarypeta profile image
hilarypeta in reply to PatV

It certainly is; Smile and the whole world smiles with you. Keep it up!

How did you find out you werent absorbing supplements?

Auntiekath profile image
Auntiekath

I was diagnosed with pd 11 years ago and for the first 9yrs nobody knew I had Parkinsons unless I told them. I am a british citizen living in France and the neurologist I saw on the onset of my parkinsons prescribed Requip I started with a low dose and was gradually increased as needed until I reached maximum dose after 9yrs. The neurologist I saw on the onset of parkinsons said to me if you do not take enough medication it does not slow the parkinsons down. But for me the medication was a great success I have parkinsons that started with trembling of my right leg. I must admit that since I have had to go on levodopa this last 2 years it is not so well controlled. Hope you find this information useful. As having a medication that worked well KI could continue with a near normal life.

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