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Sideeffect of Requip Medication

Posted: Fri Nov 21, 2008 9:39 am Post subject: Sideeffect of medication?

——————————————————————————–

My Parkinson’s medication as follows:

5 tablets Requip 2mg daily
2 ” Sinemet CR daily
1 ” Jumex 5mg

I have dorowsy and downness after taking my medication daily. I could not drive car. I am easily to be irritated.

I manage to relieve my downness by keeping myself busy. Question:

Is it sideeffect of medication?
Is it wrong dosages of medication?

Kindly advise

TeoKimHoe

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Dr. Fernandez

Joined: 20 Jan 2007
Posts: 90

Posted: Sat Nov 22, 2008 10:28 am Post subject:

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All three of your PD medications can cause drowsiness. But of the three, if I were to choose which is the most likely culprit, I would say it is the the requip.

Typically, we give requip and sinemet 3 times per day. Then we can titrate further from there.

Yours,
_________________
Hubert H. Fernandez

Anonymous
Posted: Wed Dec 03, 2008 1:21 am Post subject:

I understand that constant taking of the drug, Requip, may result on various side-effects, the symptoms depending on individual users. Requip may likely cause feelings of nausea, vomiting, constipation, heartburn sensations brought about by gastric, dizziness, drowsiness, weakness, unusual sweating (without assertion), headache, blurred vision, and dry feeling in the mouth. Some other side-effects may include difficulty in movement or walking, mental/mood changes, feelings of confusion, depression, hallucinations and difficulty in sleeping. Requip also may cause one to experience unusual urges, i.e. sexual urges or impulsive urge to gamble. Requip also caused one to suffer from low blood pressure and difficulty in breathing. Question: 1. Will Requip cause one to suffer from erectile dysfunction? 2. Will Requip cause blood clot in the body system? This is pertinent because after taking Requip for 2 years, I had blood clots in my brain. This did not happen before I started taking the said medicine. Kindly advise TeoKimHoe
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Dr. FernandezJoined: 20 Jan 2007Posts: 90
Posted: Wed Dec 03, 2008 5:32 pm Post subject:

While anything is possible, my instincts tell me that the two side effects you listed are probably unrelated to requip. Yours,_________________Hubert H. Fernandez

REQUIP AND COMPULSIVE BEHAVIOUR

Dear Doctor,
I understand that constant taking of the drug, Requip, may result on various side-effects, the symptoms depending on individual users.
Requip may likely cause feelings of nausea, vomiting, constipation, heartburn sensations brought about by gastric, dizziness, drowsiness, weakness, unusual sweating (without assertion), headache, blurred vision, and dry feeling in the mouth.
Some other side-effects may include difficulty in movement or walking, mental/mood changes, feelings of confusion, depression, hallucinations and difficulty in sleeping.
Requip also may cause one to experience unusual urges, i.e. sexual urges or impulsive urge to gamble.
Requip also caused one to suffer from low blood pressure and difficulty in breathing.
Question:
1. Will Requip cause one to suffer from erectile dysfunction?
2. Will Requip cause blood clot in the body system? This is pertinent because after taking Requip for 2 years, I had blood clots in my brain. This did not happen before I started taking the said medicine.
Kindly advise
TeoKimHoe

emotional and physical symptoms

There are emotional and physical symptoms of parkinson’s
Physician  finds difficulty to treat emotional disorders as they are complicated. They leave it to  psychiatrist .
Emotional Symptoms:

Sadness throughout the day, nearly every day

Loss of interest in or enjoyment of your favorite activities

Feeling of worthlessness

Excessive or inappropriate feelings of guilt

Thoughts of death or suicide

Trouble making decisions

Physical Symptoms:

Fatigue or lack of energy

Sleeping too much or too little

Change in appetite or weight

Trouble concentrating

Aches and pains

Restlessness

Requip sideeffect

http://www.patientslikeme.com/forum/show/5207?view=last#385548

Inaccuracies of clinical diagnosis of parkinson’s

The illiteracy by patients and complacency by physicians are the inaccuracies of clinical diagnosis of parkinson’s.

People who have parkinson’s have to continue their visit for life. physician will need to monitor the effectiveness of your medication.

Too often some physicians become complacent with their patients.

There are reasons that your doctor is becoming complacent

He or she fails to answer your questions to your satisfaction.
He or she seems “put out” by your questions.
He or she doesn’t seem to be aware of the newest medications or procedures for your condition.
He or she doesn’t seem concerned or interested that you are developing new symptoms.
He or she doesn’t allow sufficient time for discussion or questions during your exam.
Illiteracy by patients:
Denial. Helplessness. Anger. Withdrawal from social circles. These are all forms of coping with Parkinson’s Disease that may manifest themselves on diagnoses. It’s not uncommon for patient’s to begin avoiding doctor’s appointments, or refusing to take their medication. All in the very human hope that the diagnosis is somehow not true.

Dr. FernandezJoined: 20 Jan 2007Posts: 90
Posted: Tue Dec 02, 2008 9:47 pm Post subject:

You could be right, but there are other parkinson conditions that are very similar to PD and sometimes, it really is a tough call. Sometimes, no matter how hard I look and think, I find myself scratching my head. And I know it is not because of lack of effort or complacency. Yours,_________________Hubert H. Fernandez

How is the Diagnsis Made?

How is the Diagnosis Made?

Dear Doctor,

As some Neurologists are not specialised with PD, they have wrongly or inaccurately diagnosed their patients as an ageing disease. Especially when the patients are at an early stage of PD or having stress and anxiety at work.

This is very common in our country, as there is a shortage of PD doctors.

Therefore some PD sufferers die from other diseases that were made worse by PD.

Kindly detail how to make an accurate diagnosis of PD?

Thanks.

TEO KIM HOE

Dear Teo,

These are based on the four cardinal symptoms:
- Slowness
- Stiffness
- Unsteady gait
- Resting tremors

Supportive evidence:
- One side of the body is more affected than the other
- Masked facies
- Shuffling gait
- Improvement with levodopa

Dr. Ramon L Rodriguez, MD

Dear Doctor,

What if there is no resting tremor but only an action tremor, along with stiffness and slowness? Does this indicate anything different?

TEO KIM HOE

Dear Teo,

It is common to have a little action tremor with PD. You may also have PD and ET. It is best to see a movement disorders neurologist and get this point sorted out. ET stands for essential tremor which is a postural-action tremor rather than a resting tremor. There are also other tremors.

Dr. Michael S. Okun, M.D.

I was finally diagnosed as a Parkinson’s patient in the year 2005. It took me seven years before being diagnosed as such. I had seen three neurologists over the seven-year period in three different countries.

The first neurologist told me that I was in the process of ageing and that I was normal. I was also treated as normal by the second neurologist in another country.

I was very fortunate that I was in the early stage of Parkinson’s and my disease progression was slow. Regular exercises and medications relieve me from body stiffness and mobility. I thank Dr. Chew Nee Kong (Kuala Lumpur, Malaysia) for his excellent medications in treating my Parkinson’s disease. He is actively involved in raising the awareness of Parkinson’s in Malaysia. I give him double bonus for his unselfish service for the care and welfare of Parkinson’s patients – to help PD patients be more aware of their own illness and to encourage the setting up of support groups to educate the patients and their immediate family members.

TEO KIM HOE

Diagnosis of PD – Disability Rating Scales

In helping the diagnosis of PD, there are two disability rating scales used:

1. Conventionally, diagnosis is assessed based on how the current symptoms respond to treatment, ie. whether symptoms are improved by adding levodopa. It is monitored over a period of time and how the patient responds to treatment;

2. In clinical assessment, a doctor may use the Hoehn & Yahr rating scale, named after the two doctors who devised it in 1967. The Hoehn & Yahr scale allocates stages from 0 to 5 to indicate the relative level of disability that the PD patient is experiencing.

TEO KIM HOE

Dear Teo,

Thanks! I’m not a big fan of rating scales for clinical use.

To me the most important is how my patients feel. We use them a lot however in clinical trials because this is one of the most objective ways of determining whether a drug or intervention is working or not. None of the current scales we use is perfect. They do not capture all the signs and symptoms of PD.

Yours,
Dr. Hubert H. Fernandez, MD

Checklist of Parkinson’s Disease

The following are signs that you may develop in Parkinson’s Disease:

1. Unexplained stiffness in arms, legs, feet or hands
2. Tremors in arms, legs, feet or hands
3. Muscle or joints freeze
4. Difficulty walking and balance
5. Stooped posture
6. Soft speech
7. Small handwriting
8. Insomina, anxieties and depression for the past few years
9. Masked face

Consult a Movement Disorder specialist for checkup.

http://www.stalevo.com/info/simplystated/what_is_parkinsons_disease.jsp

Are All Tremors the Symptoms of PD?

Dear Doctor,

Are all tremors are indicative of PD?

How to screen that they are PD?

How to classify those sickness that have symptoms similar to those of PD?

What is Wilson’s disease and is it a treatable disorder?

What is Atypical Parkinson and Parkinson-plus?

Is the treatment of PD so delicate and complicated that the doctor finds difficulty to diagnose and the late treatment aggravates the PD progression – as a result PD patients die from other diseases made worse by PD itself?

Are Essential Tremor common disorders of elderly people ? Are they classifed as PD?

What about at Young-Onset Parkinson Disease (YOPD)? Are they inherited? What is the percentage of this group?

Kindly eleborate.

Thanks.

TEO KIM HOE

Dear Teo,

You ask questions that are loaded, Teo. I’m afraid if I answer all your questions, the rest of the readers will fall asleep!

In brief, not all that shakes are from Parkinson’s. There are other shaking conditions that are not from parkinsonism –such as Essential Tremor and Wilson’s disease.

Parkinsonism is a general condition where someone either shakes, is stiff, or is slow. At least 2 of these need to be satisfied. Not all three symptoms are necessary.

The most common cause of parkinsonism is PD. But parkinsonism can also be from strokes, tumors, infections, medications, etc. In addition, PD has “brothers” that look like it, but are actually different disorders. They are more commonly referred to as atypcial parkinsonism or parkinson-plus disorders.

Sometimes, it is easy to diagnose the type of parkinsonism or the cause of tremor. Sometimes, it is more challenging and one needs the help of a Movement Disorders specialist.

Yours,
Dr. Hubert H. Fernandez

Are There Different Types of PD?

Dear Doctor,

Are there different types of PD?

Are some worse than others?

Thank you

TEO KIM HOE

Dear Teo,

Yes, we believe PD has many subtypes and some may even be genetic. We have identified many genes such as Parkin, LRRK2, DJ1 and PINK1. We have also noticed that PD with resting tremor may have a different prognosis (better) than PD without it. Finally there are several parkinsonian syndromes which seem to respond less well to PD medications (PSP, MSA, CBD, etc.).

Dr. Michael S. Okun, M.D.

Dear Doctor,

What does resting tremor mean?

Thank you.

TEO KIM HOE

Dear Teo,

A resting tremor is a tremor at rest (ie. when not performing action). It is the most common tremor associated with PD. There are other types of tremors when one holds a posture or performs an action.

Dr. Michael S. Okun, M.D.

Dear Dr. Okun,

In view to your article above, I am quite interested to find out from you what are the types of PD associated with genetic? My family has three PD patients and I am sure they are all interested to find out from you i.e. many genes such as Parkin, LRRK2, DJ1, and PINK1. As they are medical terms, it is difficult for us to understand. We would be pleased if you could elaborate further.

What are the types of PD that are not responding well to PD medications?

Lord bless. Thanks.

TEO KIM HOE

Dear Teo,

I rarely say this, but you are asking lots and lots of general questions and I would really like to be sure that you are not diverting attention from others who have important questions to ask about themselves and about others. You will find an update on genetics that I placed with a recent abstract. Thanks for your enthusiasm.

Dr. Michael S. Okun, M.

Although large investments are spent on Parkinson’s, there is still shortage of PD neurologists.

There are four PD neurologists in Singapore and one in Malaysia.

As a result, PD patients were wrongly diagnosed by doctors as a process of ageing. Such wrong diagnosis caused the patients’ suffering to be aggravated.

I feel sorry for them.

TEO KIM HOE

Dear Teo,

I am very sorry that information, resources, and neurologists specializing in PD are all so scarce.

I very much hope that this news will spur more research, and cause more physicians to become aware of PD and the need for accurate diagnosis.

Your posts have made me aware of the great need that exists in your area of the world, and doubtless, in other countries as well.

Best regards,
Dr. Kathrynne Holden, MS, RD

Shortage of Movement Disorder Doctors

PD is a progressive and chronic disease.

Unfortunately we do not have any way of checking from where it comes to our body?

While a human grows older, the chances of having PD are higher, as their movement goes slow as well as developing a bad body posture. Tremors are the common in old age or resulting from anxiety and depression at work.

It is difficult to check on people at the age above 60 years old whether they have PD or merely showing signs of old age.

With the growth of the aged population, there is a shortage of Movement Disorder specialists in our country. It makes it even more difficult to have a correct and accurate diagnosis of our disease.

Therefore most people die from aspiration pneumonia, a fatally complicated disease.

Besides, as we do not have enough Movement Disorder specialists, it takes 2 to 3 weeks to make an appointment. This is especially worse in the remote areas.

We only have four PD specialists in Singapore and one in Malaysia.

Best regards,
TEO KIM HOE

Dear Teo,

I did not realize there were so few Parkinson specialists in your country; that must make it even more difficult to get an accurate diagnosis of PD.

Good for you for taking such an active part in your own health care — you have studied and researched PD and learned the best ways to fight it and stay healthy, and minimize the symptoms.

That will certainly stand you in good stead!

Best regards,

Kathrynne Holden, MS, RD

In view of the growth of aged population in Singapore, there are shortages of Movement Disorder specialists.

It takes 3-4 weeks to make appointments with the doctors in the government hospitals.

Public and private charity organizations have been encouraged to give more scholarships to medical students to pursue the course in order to cope with the shortage. Support groups and caregivers of PD have to work hard to increase public awareness of PD and they are the sources of help for all PD patients and caregivers.

Thanks.

TEO KIM HOE

Dear Teo,

I agree with you. PD is a rich man disease and I feel that the support in Singapore is not sufficient too.

If you go to the government hospital, getting an appointment can be up to 4 weeks or even longer. Doctors are unreachable and when you page for the doctors, it is at their own discretion to return your call.

Unless you have the money to go to a private clinic, where the doctors are more willing to talk to you but for the long term, this is a very heavy burden for the average income family.

My mother had PD at a young age of 40 and she is now 48. Her health is deteriorating. Her medications are expensive and she now has muscle aches, hallucination and her emotions are often unstable.

Under the extreme working pressure in Singapore, it is difficult to dedicate enough time for her.

It makes me sad that I am unable to relieve her of pain and agony. PD would require the combined care of a nutritionist, psychiatrist, physiotherapist and a good PD doctor. In Singapore, all of them are expensive.

Yours sincerely,
Angeline Lua

Dear Angelina,

You might post your questions to “Ask the Doctor.”

The doctors are all excellent PD specialists, and may be able to give you some guidance for your mother’s next doctor appointment — perhaps questions to ask her doctor, comments regarding the kind and amounts of medications she is using, etc.

If you have nutrition-related questions, I will help if I can.

Best regards,
Dr. Kathrynne Holden, MS, RD

Dear Teo,

I hope very much that your information and posts will help to raise public awareness of PD in your country. You might like to let the support groups know that National Parkinson Foundation will send informative booklets at no cost, and will also answer questions here on the “Discussion Corner.” I wish you and the PD groups the very best!

Best regards,
Dr. Kathrynne Holden, MS, RD

Are There Resemblances between PD and Alzheimer’s disease?

Dear Doctor,

PD and Alzheimer’s Disease are related with the Body, Mind and Soul slowdown mechanism. It degenerates your nervous mechanism i.e Body, Mind and Soul.

PD develops Dementia. There are about 40-80% of PD patients who are facing difficulties in making judgment, calculating and abstraction.

Are there resemblances between PD and Alzheimer’s disease?

TEO KIM HOE

Dear Teo,

These diseases are very different. They are similar in that they are neurodegenerative, but their course, pathology, and manifestations are very different.

Dr. Michael S. Okun, M.D.

Sideeffect of Requip Medication

Posted: Fri Nov 21, 2008 9:39 am Post subject: Sideeffect of medication?

——————————————————————————–

My Parkinson’s medication as follows:

5 tablets Requip 2mg daily
2 ” Sinemet CR daily
1 ” Jumex 5mg

I have dorowsy and downness after taking my medication daily. I could not drive car. I am easily to be irritated.

I manage to relieve my downness by keeping myself busy. Question:

Is it sideeffect of medication?
Is it wrong dosages of medication?

Kindly advise

TeoKimHoe

Back to top

Dr. Fernandez

Joined: 20 Jan 2007
Posts: 90

Posted: Sat Nov 22, 2008 10:28 am Post subject:

——————————————————————————–

All three of your PD medications can cause drowsiness. But of the three, if I were to choose which is the most likely culprit, I would say it is the the requip.

Typically, we give requip and sinemet 3 times per day. Then we can titrate further from there.

Yours,
_________________
Hubert H. Fernandez

Anonymous
Posted: Wed Dec 03, 2008 1:21 am Post subject:

I understand that constant taking of the drug, Requip, may result on various side-effects, the symptoms depending on individual users. Requip may likely cause feelings of nausea, vomiting, constipation, heartburn sensations brought about by gastric, dizziness, drowsiness, weakness, unusual sweating (without assertion), headache, blurred vision, and dry feeling in the mouth. Some other side-effects may include difficulty in movement or walking, mental/mood changes, feelings of confusion, depression, hallucinations and difficulty in sleeping. Requip also may cause one to experience unusual urges, i.e. sexual urges or impulsive urge to gamble. Requip also caused one to suffer from low blood pressure and difficulty in breathing. Question: 1. Will Requip cause one to suffer from erectile dysfunction? 2. Will Requip cause blood clot in the body system? This is pertinent because after taking Requip for 2 years, I had blood clots in my brain. This did not happen before I started taking the said medicine. Kindly advise TeoKimHoe
Back to top

Dr. FernandezJoined: 20 Jan 2007Posts: 90
Posted: Wed Dec 03, 2008 5:32 pm Post subject:

While anything is possible, my instincts tell me that the two side effects you listed are probably unrelated to requip. Yours,_________________Hubert H. Fernandez

Characteristic of parkinson’s

Posted: Sun Oct 19, 2008 6:46 pm Post subject: Parkinson’s Patients: Mercy Killing or Senseless Suicide?

I think some patients choose to suffering Mercy Killing or Senseless Suicide as He/She has no trust and believe on the doctors and prefer what he/she is? I have a friend who has parkinson’s disease for many years though he is wealthy but he does not believe and trust doctor he prefers to stay what he is. He is believing it will go away “magically.

 There are   five stages of emotional response: denial, bargaining, anger, despair and acceptance.* pHe pleads mercy killing. He believes he has other diseases rather the parkinson’s. I feel sorry for his decision. This is his choice to plead mercy killing/Senselesss suicide rather by treatment

 Therefore Illiteracy by him towards the diseases are the main cause of parkinson’s scenario.

  These are all forms of  coping with Parkinson’s Disease that may manifest themselves on diagnoses. It’s not uncommon for patient’s to begin avoiding doctor’s appointments, or refusing to take their medication. All in the very human hope that the diagnosis is somehow not true. Ultimately it is important to confront the diagnosis as timely treatment and making changes to one’s lifestyle can make a huge difference in living with Parkinson’s Disease.

Apathy is a  characteristic of Parkinson disease. Apathetic behavior is not something the patient can voluntarily control, and it is not laziness or the patient trying to be difficult — it is a symptom of Parkinson disease.”

 Apathy :  indifference, unconcern, lifelessness, uninterested, dullness, listless, uninquisitiveness, lack of emotions or feeling,etc  

Dr. FernandezJoined: 20 Jan 2007Posts: 90
Posted: Mon Oct 20, 2008 8:48 pm Post subject:

I am sorry to hear this, as PD, although not curable, can be treated. A lot of our patients live very meaningful lives. Each person has a right to his or her own beliefs, but I just hope that this decision is not a result of ignorance or lack of education/information. He should at least see a Movement Disorders specialist, even just once before he makes his decision. I wish I can do more. My thoughts are with your family. Yours,_________________Hubert H. Fernandez

http://www.gulfmd.com/rresponse/Euthanasia_wdyt.asp
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Anonymous
Posted: Wed Oct 22, 2008 11:38 pm Post subject: suicide

My meds were “off”. Statue-like in my garage; I watched all of the neighbor ladies drive by in their golf carts. In the nick of time; my sinemet started kicking in. I grabbed my crutches and hobbled to my golf cart. I drove to the starter shack and schleppe up to the starter’s window.. The starter didn’t say the words. They were in his eyes. I responded with, “In 15 minutes; my meds will kick in and I’ll have a hole in one. You just watch!” Big Mouth!! Several people watched as I landed my tee shot 12 inches from the cup. I hollered, “Better living through chemistry and my Gator docs!” My point is this…we can still achieve wonderful accomplishments. Get past your stubborn refusal to learn how to live better, despite PD. Now my bucket list does not include climbing Mount Everest. It never did. But, still, I would love a hole in one. Many wonderful people and achievements have come to me since PD. More will come. Suicide only hurts the people who love you the most. You wouldn’t be there to feel their pain. More than one member of my family has gone the suicide route; so I know whereof I speak. GROW UP!! Suicide is for self-centered cowards. Sure; it takes courage to face this disease. But, we are not alone. We have a dedicated team in our corner. You know several of them…Drs. Fernandez, Foote, Hauser, Mandel, Nieves, Okun, Rodriguez and Skidmore. These bright young medical sleuths put in 80+ hours in clinic, teaching and research a week….then volunteer stuff like “ATD” and “hawgwildcure.com”. They learn from us; we from them. Every coping strategy we implement is a small win. Every new med that buys another few hours of “on” time is another win. We will win the biggest jackpot of alll when a cure is foound..during our lifetime! We just need to keep living so we’re still here when a cure is found. It will be found. Betcha!!!! And, I’m not on mirapex or requip! I know that few Parkies, actually, do commit suicide. Our docs will elaborate on that…please. Ths is no dress rehearsal, Judy
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Dr. FernandezJoined: 20 Jan 2007Posts: 90
Posted: Fri Oct 24, 2008 10:12 am Post subject:

Thank you, Judy, as always! Your words can sometimes be tought to swallow, but they are real and they hit us right in the core. Yes, I believe in fighting and living life to the fullest. I believe in hope and I believe in contributing to that hope. Like you, and millions of others with PD, giving up is not in my vocabulary! Passive suicide due to ignorance is one thing, and active suicide as part of depression is another. I really believe knowledge is power. And I do hope that there will be less and less people in this world who are “giving up” simply because they do not know any better. They do not know that there are medications and strategies to make their lives better and more manageable. They do not know that PD is not a deadly disease that goes for the jugular in months. It is a slow process that can stick with you for years or even decades and ignoring it just makes your life more miserable. Depression however is common in PD. It occurs in up to 50% of PD patients. And suicidal thoughts can be part of it. In fact we featured this as our article of the month at the Movement Disorders Society Web Site (www.movementdisorders.org). The good news is that this can be treated. Our medications work! So, passive suicide from ignorance can be treated with education and active suicide from depression can be treated with medication and therapy. More power to you all! Take care,_________________Hubert H. Fernandez 

Nutrients

Nutrients

Antioxidants

Dear Doctor,

Is it true that nutrients’ intake must be added if we do more exercises, as exercises may reduce the level of antioxidants in our blood?

Does Jumex have an impact on the amount of nutrients intake? Jumex contains long term neuron-protective properties. However, it also increases cellular energy production that has potentially negative effects. The enhanced cellular function increases free radicals and aggravates stress. It may be necessary to periodically re-adjust the nutrients to put back the appropriate level of antioxidants in our blood.

Kindly advise.

Thanks.

TEO KIM HOE

Dear Teo,

In the case of exercises, generally only athletes need to be concerned about additional nutrients. Humans evolved to hunt, run, gather food, and otherwise, engage in physical labor, and meet their nutrient needs with their normal daily diet. Athletes, however, have a much higher activity level than normal, and may need extra nutrients.

Water is an exception. This most vital of all nutrients is easily lost by all humans and needs to be constantly replenished.

In the case of people with PD, there is an additional factor. PD is stressful and stress produces free radicals, and thus cellular damage. While there is no evidence that dietary nutrients can have an effect upon the area of the brain affected by PD, diet most certainly affects the health otherwise. Here, the first line of defense is a nourishing diet. Foods contain an array and balance of phytochemicals, flavonoids, vitamins and minerals that cannot be duplicated in pills and other supplements. Vegetables, fruits, nuts and seeds, whole grains, cooked legumes, and fish should be the backbone and mainstay of the daily diet. A multivitamin supplement is a good addition, but does not take the place of foods. An annual physical examination with lab tests will determine whether there is a need for other supplements, and this certainly can be the case as we age – vitamin B12, for example, is less well absorbed.

Jumex (selegeline), and in fact all PD medications, can have undesirable side effects that increase various kinds of stress, and here again, a wholesome diet, plus exercise, is the best way to combat these effects. You are doing exactly the right things in following a good exercise program and eating healthful foods.

Best regards,
Dr. Kathrynne Holden, MS, RD

Dear Doctor,

Thank you for your excellent reply.

However, I still believe that when we do more exercises, we would need more nutrients to protect our body from oxidative stress, whether or not we are an athlete.

The increasing energy production in the cells (from some medications, exercises, stress, etc.) will increase free radicals production. This is the natural biological process in the body.

But regular exercising will also increase endogenous antioxidant enzyme that enhances antioxidant mechanism in the overall body.

The aging process, antioxidant level and oxidative stress are dynamic processes which we have to monitor every 6 months or annually, at least, i.e. through blood test on the nutrient levels.

I understand that most PD patients have deficiencies or decreased antioxidants, folic acid and Vitamin B12 or 6, and these deficiencies occur in normal old adults too.

To improve our nutrient level in a natural and safe way, we need to have more fruits, vegetables and fish (source of co-enzyme Q10).

Kindly advise.

Best regards,
TEO KIM HOE

Dear Teo,

Yes, it’s very true that exercises, medications, and in fact, even metabolizing the food we eat, result in the production of free radicals. However, a healthy human body is very well adapted to combat these free radicals by producing its own metabolic pathways and enzymes to quench the free radicals. The key, first and foremost, is a high-quality diet that supports the production of such enzymes – as you say, fruits, vegetables, and fish are excellent.

Having said that however, this can change with age, disease conditions (such as PD) and many types of medications. That is why CoQ10 (co-enzyme Q10) and creatine are being studied, to see if they can help alleviate the negative effects suffered by PD patients. It is also good to remember that long-time use of levodopa can result in higher levels of homocysteine in the blood, and if this happens, supplements of B vitamins are needed.

Best regards,
Dr. Kathrynne Holden, MS, RD

Dear Doctor,

I wish to add the following to my earlier email.

The level of nutrients in our body depends on 3 factors:

1. The amounts of nutrient taken from food and supplements.

2. Ability of intestinal absorption.

3. Utilization of nutrients by our body, depending upon our level of physical activity. If we do more exercises, we will need more nutrients, hence affecting the level of antioxidants in our body.

Thanks.

TEO KIM HOE

Anonymous said…
its important to note that being a ‘weekend warrior’increases free radicals but not your antioxidant defences… i got a free of proleva and it really seems to help with my energy…
www.proleva.com/antioxidants/

words by Dr.Kridakorn

 It was 3 years ago that I first met with Mr. Teo.  At first glance I am afraid to say that he wasn’t looking very well.  I can’t blame him.  He was recently diagnosed with Parkinson’s disease, a debilitating neurodegenrative disease.  Current medical treatment is symptomatic and there is no know cure.  This news could depress even the most optimistic person.  Mr.Teo has actually been the opposite of depressed.  He has taken this challenge head on!  

Parkisnon’s is a progressive neuro-degenerative disease – in other words it only gets worse.  It has been nothing short of miraculaous to see Mr.Teo actually improving! 

I have had the opportunity to work with Mr.Teo as one of the many doctors that he consults with in his comprehensive approach to find a better way to treat Parkinson’s disease.  What we do know is that Parkisnon’s wreck havoc on the nervous system through oxidative damage.  We tested him and improved his antioxidant status thorough a tailor-made nutriceutical program.  We worked with hormone replacement to boost is internal systems. 

Mr.Teo also exercises regularly and practices yoga.  I believe that this comprehensive approach has helped him to greatly improve his balance.

Another important part of his success I believe is from Ms.        Lee – his wife.  Few are blessed with such an exceptionally supportive life partner.

What I am most impressed with – even more so than his results – is Mr.Teo himself.  He is eager to learn and ready to share the information and experiences that he uncovers.  I would like to encourage all sufferers from Parkinson’s e to visit his Blog (WWW.HEROTEO.COM) . 

It is an honour to be part of his doctor team.

Dr. Kridakorn Watcharachotpimai,American Board of Anti-Aging Medicine