Don't give up hope.

[richann]

I've been a caregiver more than once for long period of time. Maybe you can find my first post in the forum. Ann Carlisle. What I've learned is that the foolish position studies disease, while the wise position studies health ! Parkinson's - the title. That's not who your loved one is ! We managed for a couple of years for my husband not to hear that word and claim it for himself. He had a prostate problem last summer and was in the hospital 3 times, finally having surgery - so he could urinate. Then he was branded with PD ! Summer set him bsck quite a bit and we ended up with visiting nurse home care. One of the therapists, a man, was good and we all learned more about how to help my husband regain what he had lost and how to walk, get in and out of bed, etc. I have been in a health related business for 17 years and learned that drugs, with their many side effects, only address symptom, not root causes, so my family is not taking any drugs, with the exception- the drug for the tremors, which we have now stopped, with no problem! Yeah !! I discovered new treatment for just about every condition. The 21st century is bringing old knowledge through technology. Since Sept we have beenn using energy medicine. It's the way of the future in health. In Jan. we received more information and a new exclusive product which we, even the whole family, are using. My husband, 88 in March, can now walk by himself though uses the walker some for security and pushes it like a grocedry cart instead of using it as he's supposed to. very proud of himself when he walks without it. The wheelchair is in the garage gathering dust. If any of youwant to learn what we're doing you can go to www.globalteamelite.com/myac - a web site for information. You cannot buy from it, but you could send a message to me for more information. I listen to the naturopath doctor who is responsible for bringing this to the world. It all makes sense ! ! ! listen to her on conference calls every week so can learn more.. Amazing woman and you can Google her on the Internet. For myself, I'm 84 and the caregiving was having me on ice for pain daily - until I used the energy medicine. I now can work a 10-12 hour day without paying for it in pain so have been "detailing" our 5bedroom home, room by room! Another yeah !
The patient may have non-related to PD issues - constipation - try prunes and oatmeal. lots of water, live food -meaning fresh and local or oganic if possible. In the hospitals and nursing homes, the food is awful - mostly out of cans or boxes, refined/processed food, and mass produced for the patients. God has given us self-induces healing abilities. The body can heal itself. Blessings to all of you. Ann

[mona47]

Are you saying your husbang stopped taking all his parkinsons medicine and is doing better,because of this product/

[heather]

Mona please be very careful
don't forget what works for one doesn't work for others
I have tried doing some research into this, and can't seem to find out , much about it, other than the link, which is more of a sale's link

have been trying to find out how many people % have trialled it, and at what success and age group,
For instance if only say for argument 30 [ to low a number to do a trial on ] have tried it how many have the same result of success, how many had no success
what age group is very important, for many reasons
etc etc etc


please remember never never stop your treatment till you are 100% sure it will work, and that you have someone to contact
face to face or phone call, as e-mail correspondence never works


please remember this is only my thought's.

But after almost 40 years as a qualified nurse, and almost 29 years as a Community nurse, and a diploma in research, I am always very very careful, before i go down paths that I'm not sure of
it's very difficult to turn the clock back, if things go wrong

Some may think it's easy for me to say this, as I don't have PD, but i would be the first to go for it if there was more research done that proved it worked, and i'm sure some neurologists would be trialling it as well

please remember this is just my opinion, may be someone else has a different opinion, it would be nice to hear it


This is the declaration at the end of the link above

* Disclaimer: These statements have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat or cure any disease.

[suzie Q]

Hi Mona Heather is right .Make sure you have checked it all out it does seem a little suss i looked at the website and it did not seem to give a lot of information so be careful

Bye for now Sue

[heather]

Hi Both
like i said you need to be able to contact the person or company [for want of a better word] direct. It looks like you can only go through Ann, and in her first posting says she is "in business"
I could be wrong, and apologise if i am, maybe i'm reading it all wrong
please just be careful, I truly no what it's like to clutch at straw, I would do anything, to get Jim well again, but i also don't want or need to make him worse, and like i said. you can't turn the clock back

[DAH]

Hello Ann; I hope I am doing this correctly. I'm not to computer savy. I just read your note of Feb. 'o9. My husband has had PD. for almost 3 yrs. now. He is taking Mirpex and has just started taking levadopa, a small am't. His movement is slower but otherwise is is doing alright. The physician suggested he use Creatine since it seems to be doing good for the PD patient. He did not know the proper dosage. I placed him on COq10 1200 mg/day when he was first diagnosed with PD. The DR. said he felt the COq10 was expensive and studies show it is not as good as Creatine. Do you know anything about this. I would appreciate any info you can give. Thanks, God Bless, Dottie Hand

[heather]

Hi D A H
afraid Ann never came back