I’m only 23 years old dealing with all this
Parkinson’s : I’m only 23 years old dealing... - Cure Parkinson's
Parkinson’s
Written by
starlove1995
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32 Replies
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Sorry.
But, the good news is that at your age, if you pull out all the stops now, vigorous exercise, get fit, diet, other lifestyle changes, etc., you have a very good chance of, and might well, lead a normal life.
What's normal life worth?
You have to work at it.
What are some good foods u Recommend I eat ?
Put, "nutrition and Parkinson's disease" in a search engine window - then stand back.
Everybody's all over the map on this. There are a few fundamentals. Stay away from sugar, corn syrup, or vegetable oil. Beyond that, you're on your own.
I try to eat low-carb, mostly fish and vegetables. Modest protein and minimal meat. I don't pay much attention to fat consumption. My own version of a Mediterranean diet. Nothing that comes in a can or box, no gluten, bread, dairy, processed food, fried food, fast food.
gluten free and sugar free, not easy though
Research Ketogenic diet. And organic whole food. The goal is to reduce your body burden of toxins.
Ok
So like green things are ok
Healthy at that
Yes you will learn a lot here, welcome!
Seems to me the guy dealing the cards is a bastard 
What?
I mean it's a rotten break to get PD at all. A particularly rotten break to get it your age. MBanderson clearly has much more experience in this area than I do, so I take heart from his optimism for your outlook.
The internet says the same thing as well
I share what they wrote MBAnderson, Dreem, ConnieD and John Pepper showing sensitivity towards starlove1995. At her young age there is a strong need for optimism, encouragement and experiences. He has a long way to go.
Hi starlove. My first symptom arrived, uninvited , at the age of 29. I am now 84 years old and have no longer needed to take medication since 2002. What I do to stay healthy costs nothing. I am selling nothing, other than my book, which you don't have to buy, I will help you to get better anyway.
Look at my website - revereseparkinsons.net and contact me, I will try to help you.
The website not working
I trust a lot of john pepper's info. Just keep in mind that not everything works for every one the same way. Dont spend your money on anything till you reveiw, this is a good place to check for reveiws. Keep a log of what you do and how it makes you feel. And always one day at a time. Dont worry about how you may be a year from now. I am about the same as i was 7 years ago.
🔴 CAUTION: The 'johnpepper' avatar/member is suspected by some to be a malicious bot/virus infecting the Healthunlocked PD forum. It typically pops up in the posts/inquiries of new, unsuspecting members (veteran members generally ignore it) and invariably alludes to a magical formula (thus far never replicated) by which faithful followers will supposedly be able to "Reverse Parkinson's Disease".
As is typical of such pesky bots, your actual questions/concerns rarely factor into its auto-reply feature which is programmed simply to announce that "meds don’t work" while directing the unsuspecting newcomer to "look at my website". Once there you will find yourself expected to wade through lengthy tracts of a rank amateur's mind-numbing misinterpretations of science (if/when the site is functioning). This is one rabbit-hole you’d best avoid if it's GENUINE solutions you seek.
Wow ........... why not say what you really think ......... lol
I have found John Pepper very helpful. He is advocating exercise, especially fast walking, as an aid to a better life as a PwP.
Uh huh... the idea that 'exercise is good for you' is a pretty revolutionary concept (for some). It will NEVER "reverse" PD as the JP-bot contends however...
If he confined himself to recommending exercise few would object. Exercise is almost universally advocated as beneficial for PWP. (Although, some like my Dad, who has severe postural hypotension are unable to participate in this therapy - well, certainly not fast walking). The problem I think PDC and others object to is his insistence his is the ONLY way, his manifest ignorance of science, and the potentially dangerous suggestion that PWP should follow him in preference to their qualified neurologist. Much of what he suggests probably makes good sense. It's the way in which he says it, that represents the potential danger. Among the bits of science he appears to have a flaky understanding of is "What is Parkinsons disease?"
I have no problem with civil disagreement. I just don’t see the point of mocking him or anyone else.
Yes I agree about being civil. Maybe JP means well. I haven't yet met anybody else making such authoritarian statements that are manifestly incorrect, and very unhelpful as JP. I am thinking in particular of his comments regarding GDNF and the Bristol trials, where he claimed toxicity in spite of clear evidence that he was mistaken. I think it important to refute such errors. Ideally get the false statements withdrawn and the posts deleted.
Yes. I noted the GDNF comments as well. I agree in general about refuting false statements. But some beliefs are so tightly held I don’t know if it is worth the effort to refute them. I find this site quite valuable because of the willingness of the community to freely share information and experience.
I do think JP means well and is simply trying to share something he believes works. He can be a bit strident but he thinks he has valuable information to share. I don’t think he deserves to be mocked by anyone and I am not going to continue witnessing the mocking and say nothing.
As many of you know already, I joined this group because my husband had PD and died of aspiration pneumonia this year at age 81. I have some mild features in common, but never felt it necessary to do anything about them: bad balance problems, no arm swinging and intentional tremor. John was very helpful with the balance. I also looked at videos in which people were able to jettison their wheelchairs and walk again with his aid.
I apologize for PDConscience. He is our resident bully.
A young lady come here for help and some people started to argue ignoring the fact that everyone has the right to express his/her opinions, no matter how often.
Starlove, for now it seems the exercising (dancing, fastwalking , pushups, swimming etc) and the Thiamine HCL help a lot. I do not know about the diet if it is worth to try it but you can try it if you want. I tried it but I gave up.
And try to avoid stress as much as possible, especially the stress of knowing of having such a disease or the stress caused by certain people. Some people have it for long time and they are ok, some have it for few years and are in worse shape.
Wish you the best!
Thank u
My heart goes out for you, was your prognosis confirm and am praying for a cure
Hi,
Start on vitamin B1 and mannitol and red light therapy to have neuro genesis.
Also fish oil n good probiotics . You can read all about these things on HU
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