Muscle spasms... I was hospitalized for a week with severe muscle spasms... I was not able to even walk. After a week of test, etc... The nurse told me to try vitamin E 400 units a day. And after months of suffering with muscle spasms... Vitamin E cured them in just a couple of days. That's been about 40 years ago and I still take one everyday. No more than 400 units a day.
Thx. My husband abdominal cramps seems no one yet has heard about this. We will try vit E Been to emerg lots no one knows. Told to take Tylenol. Had to get adult businessy son to say I never saw my dad cry in his life I asked can you give him muscle relaxer fought for it unbelievable in 2024 thx so so much for commenting Judy ❤
I’ve had several scans following mobility issues; constant headaches; neurology referrals….for a year now. And all Doctors seem to tell me is ‘let’s review in six months’ ! Which leaves me with symptoms yet no diagnosis much less advice or even dietary recommendations ! I’ve researched the symptoms I have which has led me here. I’ve learned more in a twenty minute video than from any consult so far ! Thank you
You are not alone, this happens with my grandpa too. I have found on my own through research that inflammation is a huge contributor to all disease and significantly impacts patients with parkinsons. Eating an anti-inflammatory diet would make a drastic relief. I also found a vitamin it's called "Source of Life, Liquid Gold" that by itself has proven more effective than sinemet (at least for my grandpa) when it comes to tremor, gait issues, and speech and constipation.
Some 8 months ago I hiked with my brother who noticed that I wasn't swinging my arms when walking and that I dragged my feet when tired. He suggested I see my doctor who I haven't consulted in many years as my health had been excellent throughout my working life (to age 69). I am now 76 and before seeing my doctor I researched my conditions and came to the conclusion that I had Parkinson's. I was unable to make an appointment to see a doctor at my surgery and was forced to see a trainee doctor! He didn't think I had the condition and called the senior partner who after ten minutes of inquiries and assessment also said that she didn't think so either. I persisted so she sent me to see a neurologist who did indeed confirm Parkinson's. That was in September 2022 and I haven't seen anyone at the doctor's surgery since. I should mention that I was advised to take statins for my cholesterol - which I refused! Do your own research I say.
I have just stumbled on this video from 5 years ago. Now I am going to search to see if this doctor has done an update to it. This was such helpful information presented in a way that was easy to understand. Thank you.
THANK YOU for the best information I have found about my PD symptoms anywhere! I’ve had it for years, seen & listened to several specialists, but actually broke into tears listening to you explain WHY I drool among several other symptoms I’ve been stumped by how to deal with, and why. GBU for helping me to realize it’s part of my Parkinson’s.
i had symptos of PD for over 3 yrs before i was finally diagnosed with PD Before that i was told i needed counseling and nothing was wrong witn me. and it was all in my head. i finally found a
Found a resolution to my constipation problem by accident. I have Non-Hogkin’s Lymphoma with a significant weight loss. As a PKD patient I had suffered from constipation for almost 10 years. My Home Health Care Provider began making the jello mixed with a clear high protein drink. Immediately, my stool became softer and I have not had constipation since.
Still not convinced I have Parkinson's...been 3 years and it feels more like Long Haul Covid. I do have more non motor (hands & feet involuntary movement) taking Carpadova/ Leprodova for tremons early on in the diagnosis. I could not walk unattended the first 2 years of diagnosis and only recently regained that ability( with some gaint problems).Thank you for all you bring to the channel..it certainly is helpful and sooooo informative.
I am not sure I have this either. I do have a lot of the symptoms, but after 27 years I am not much different, apart from dysmotility. I think I may have mitochondrial disease as my initial muscle biopsy results are showing signs of it. Or maybe I have three things wrong. As well as PNKD faulty gene, but they said this was not causing all my symptoms. Or is it that people can be different.
Fhgggufua😅iiauoußßdaydyàadfIuuuuussdsdy😅dausi😅😅❤❤❤y😊dishh😊I you😊 you you hyiiuhiiiuhhuh you 😮😮 hate uuhhh hug❤❤❤❤❤s we we eeyyqwywwwwqee tQ ate tt😂eesaddaddaqqqqqqeeu😊stywokkkh 26:04 day is how g❤❤❤❤❤❤😅❤sayf❤gwofturrrrrr
I have sensory issues and the noise from her playing with whatever is in her hands is probably going to make me leave. I hope she reads this so she doesn’t do that again going forward.
I had constipation, GI issues and "IBS "for 20+ years. I stopped using artificial sweeteners, chewing sugar free gum, etc. and my problems went away. I haven't had any problems since. It was artificial sweeteners.
I agree with pastorpresent1. Well explained, good volume and articulation. Lots of good information. I go to Duke and everything you spoke about is familiar. I experience these things often. Some even daily. Thanks for posting this . It goes along way in helping to understand what i experience.
The doctor is saying there is a probable connection between Irritable Bowel Syndrome and Parkinson's. If High Dose Thiamine Therapy ( as per Dr. Constantine) halts much progression of Parkinson's and Thiamine deficiency is very much related to the autonomic nervous system including symptoms of gastroparesis maybe the common connection is Thiamine.
I don't eat a lot of food. I can go 3 or 4 days easily without going to the bathroom. Since i am lactose intolerant i tend to eat a bowl of cereal or just drink a glass of milk to go. I didn't know that a runny nose could be a symptom. My nose runs constantly. I also have had excessive drooling the past year when i sleep. Never thought about it being a symptom as well..
@@Georgiaredfern I’m not sure but I think he’s saying if he takes milk it helps to make him ‘go’ to the toilet since he hadn’t had a ‘motion’ for days.
@@michiganmymichigan i only drink the milk when i haven't had a bowel movement in a while. I already take olive oil supplements as part of my healthy dietary regime. 👍
Thank you for discussing swallowing problems & how they can lead to weight loss. Living with PD, I try to keep nutrition drinks stocked for these times to substitute food bc I’m already underweight. I also try to drink Gatorade and extra water while dealing with no appetite times, trying to prevent more weight loss.
Crystal, you may also might try drinking a good quality Bone Broth (either buy at the store or make your own) as it has a TON of nutritional value that you may not be getting from Gatorade and it doesn't have sugar in it. Bone Broth has lots of protein
@@lisapizzale6466bone broth is great but for many with Parkinson’s, anything with animal protein affects the results of taking Levodopa. The meds won’t work because animal protein uses the same neurotransmitters as the dopamine. I can’t even have a small amount of dairy in my coffee. It’s so exhausting and tough to deal with.
My husband drinks milk at breakfast and dinner,usually 20ozs at a time. I have told him that I don't think he should be drinking that much milk. He likes his ice cream too! He is 82, what can I say ???
I have had day time drooling no control, gait, excessive, rigidity been diagnosed with RA and sjogrens but i couldnt lift my foot 1inch up just 6 years ago and now drooling, trouble swallowing all the time take days for food to get down
Wonderfull, I am so pleased to have been able to listen to this presentation. I am so convinced that I have Parkinson's disease. In 2009 I had an early diagnosis but was told I had Familial Essential by a N Tremor
Has patients being treated with carbonic/lepo been reporting increased incidence of external tooth deterioration? I submitted that question on the APA website and was shocked to get 500 positive responses in less than 24 hours.
I went for an acupuncture session and found I had so much energy. But today energy is less . Haven’t been diagnosed yet by a neurologist but have most of the early symptoms.
What do you do for a living? This common question if given unto its own fullness with all things being reconciled back to the father. The helping hand the loving hand and may only good love touch the works of your hands now and evermore.
My mother had it and she smoked i saw her druel but she was medicated with depression meds she died of neumonia double they were trying to control her body temp they put ice cubes under her arms maybe for fever she fell alot she died she was on oxygen before she died
I would like them to start studying chronic akathisia. I got chronic akathisia from trying medications. I had no idea benzodiazepines could make you this incompatible with life. I have been left tortured alive 4 years off of Klonopin. When I got hurt, and it could be nothing else, I went looking for answers. I found 200,000+ hurt doctors, nurses and patients who had been screaming about this harm online if I’d only looked. Everything that makes akathisia feel better just down regulates you and makes you one notch worse. This iatrogenic harm needs screening before anyone else is hurt. Proper informed consent does not exist. Besides, how can you give informed consent for something so awful you cannot imagine it? How bad is your sleep? How depressed are you? Enough to be left tortured alive?
If these patients have constipation, they should be fed better. Meat, fat, butter, more fatty foods and that will also feed their brains. Our brain is fat and cholesterol. Don't starve them......
I have blood pressure problems and I always hotter than my wife like that's an issue with her she can't stand the smell of old sweat on the bed and the couch and I have the shakes 3/4 of the time, the first time I was with my ex wife in '02. I also I had a major stroke in '99.
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms…My Dad is well again/
Parkinson’s patients should be getting B1, the other B vitamins and plenty of healthy animal fat and protein. Your body cannot make cholesterol without animal fat. People on vegan diet end up with brain disorders in the long term.
The only word I can use about this video is, gross! Sure this was 2015 and it's now 2023 and we have seen a significant rise in Parkinson like symptoms and people that were tricked into receiving an unauthorized covid inoculation but are you kidding me, you still don't know some of the alternative therapies that can help prevent worsening symptoms? In fact you made a statement that, as patients symptoms progress, which means that the therapies you're using don't freaking work! I treated pediatric patients and no more about treating Parkinson's than this speaker. That's a super sad statement.
Parkinson disease 🦠 is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms. My Dad is well again.
Young lady my wife died a year ago and one of the problems was Parkinson and you are helping me to understand what happened .Thankyou so much.
Muscle spasms... I was hospitalized for a week with severe muscle spasms... I was not able to even walk. After a week of test, etc... The nurse told me to try vitamin E 400 units a day. And after months of suffering with muscle spasms... Vitamin E cured them in just a couple of days. That's been about 40 years ago and I still take one everyday. No more than 400 units a day.
❤
Thx. My husband abdominal cramps seems no one yet has heard about this. We will try vit E Been to emerg lots no one knows. Told to take Tylenol. Had to get adult businessy son to say I never saw my dad cry in his life I asked can you give him muscle relaxer fought for it unbelievable in 2024 thx so so much for commenting Judy ❤
I’ve had several scans following mobility issues; constant headaches; neurology referrals….for a year now.
And all Doctors seem to tell me is ‘let’s review in six months’ !
Which leaves me with symptoms yet no diagnosis much less advice or even dietary recommendations !
I’ve researched the symptoms I have which has led me here.
I’ve learned more in a twenty minute video than from any consult so far !
Thank you
😊
You are not alone, this happens with my grandpa too. I have found on my own through research that inflammation is a huge contributor to all disease and significantly impacts patients with parkinsons. Eating an anti-inflammatory diet would make a drastic relief. I also found a vitamin it's called "Source of Life, Liquid Gold" that by itself has proven more effective than sinemet (at least for my grandpa) when it comes to tremor, gait issues, and speech and constipation.
Some 8 months ago I hiked with my brother who noticed that I wasn't swinging my arms when walking and that I dragged my feet when tired. He suggested I see my doctor who I haven't consulted in many years as my health had been excellent throughout my working life (to age 69). I am now 76 and before seeing my doctor I researched my conditions and came to the conclusion that I had Parkinson's. I was unable to make an appointment to see a doctor at my surgery and was forced to see a trainee doctor! He didn't think I had the condition and called the senior partner who after ten minutes of inquiries and assessment also said that she didn't think so either. I persisted so she sent me to see a neurologist who did indeed confirm Parkinson's. That was in September 2022 and I haven't seen anyone at the doctor's surgery since. I should mention that I was advised to take statins for my cholesterol - which I refused!
Do your own research I say.
I agree!
Bless your beautiful soul 🙏❤️🙏
This is the best discription of PK I've heard. Thank you 🙏
I hear music playing all the 🎉time. Is this audio hallucinations.
I hear music if something else is running too. Like a fan.
@@suemoo22me too! It’s so weird to me. Sometimes it’s music, sometimes it’s people talking when no one is in sight.
F
I have just stumbled on this video from 5 years ago. Now I am going to search to see if this doctor has done an update to it. This was such helpful information presented in a way that was easy to understand. Thank you.
Did you anymore research On this doctor to see if she has done an update? Thank You!
Oķ0@@maryloucoleman3300
Excellent presentation
THANK YOU for the best information I have found about my PD symptoms anywhere! I’ve had it for years, seen & listened to several specialists, but actually broke into tears listening to you explain WHY I drool among several other symptoms I’ve been stumped by how to deal with, and why. GBU for helping me to realize it’s part of my Parkinson’s.
Kjiiiiiii
Can she get to the point?
Terrible speaker.
@@kakahama1415 ooo
Pitch perfect iii cast players
@@gfitz600113:51
Thorough, professional, and interesting, well done.
Thank you.
My husband has all that you have mentioned.
Thanks, very helpful information. I’m newly diagnosed.
Great presentation. She is a terrific orator and teacher.
Fabulous speaker with great information very helpful
This is the best Parkinson's information upload I've ever seen. Very smart lady
Good information. Thanks.
What a welcome acknowledgement of symptons that many of experience but goes unnoticed befored and AFTER diagnose
i had symptos of PD for over 3 yrs before i was finally diagnosed with PD Before that i was told i needed counseling and nothing was wrong witn me. and it was all in my head. i finally found a
Neurologist, who specializes in PD.
I finally found a Doctor that believed me. She referred me to a movement disorder neurologist and he diagnosed me in about 10 minutes.
Best talk I have heard regarding PD
Thanks so much, madam, have to listen a few more times. God bless you.. 48:17
I agree. . Exercise helps so much.
I second that this is the best discussion of p.d.
Great Information and Presentation
Found a resolution to my constipation problem by accident. I have Non-Hogkin’s Lymphoma with a significant weight loss. As a PKD patient I had suffered from constipation for almost 10 years. My Home Health Care Provider began making the jello mixed with a clear high protein drink. Immediately, my stool became softer and I have not had constipation since.
Terrific information, I am shocked at the range of quality within the physician community.
aw the Q&A wasn't recorded? great video. thank you for sharing.
Still not convinced I have Parkinson's...been 3 years and it feels more like Long Haul Covid. I do have more non motor (hands & feet involuntary movement) taking Carpadova/ Leprodova for tremons early on in the diagnosis. I could not walk unattended the first 2 years of diagnosis and only recently regained that ability( with some gaint problems).Thank you for all you bring to the channel..it certainly is helpful and sooooo informative.
I am not sure I have this either. I do have a lot of the symptoms, but after 27 years I am not much different, apart from dysmotility. I think I may have mitochondrial disease as my initial muscle biopsy results are showing signs of it. Or maybe I have three things wrong. As well as PNKD faulty gene, but they said this was not causing all my symptoms. Or is it that people can be different.
Fhgggufua😅iiauoußßdaydyàadfIuuuuussdsdy😅dausi😅😅❤❤❤y😊dishh😊I you😊 you you hyiiuhiiiuhhuh you 😮😮 hate uuhhh hug❤❤❤❤❤s we we eeyyqwywwwwqee tQ ate tt😂eesaddaddaqqqqqqeeu😊stywokkkh 26:04 day is how g❤❤❤❤❤❤😅❤sayf❤gwofturrrrrr
@@suziesuzie9455 3:47
.😅
Great ideas.
Very well versed speaker !
Thank you Very,
alot to take in! very informative!
👍Agreed
Especially the part where we discover that
“…alot..,” is not a word.
They are 2 words but I see that
A LOT👍🙏😇
Beautiful presentation
I wonder if I can use these slides
My favourite aunt died with Parkinson's. I never understood it but was so sorry to lose her. She was just the most awesome person.
😅
27:24 27:25 27:25 😊😢
29:00
I have sensory issues and the noise from her playing with whatever is in her hands is probably going to make me leave. I hope she reads this so she doesn’t do that again going forward.
I wish you were my doctor ❤
Appreciate the information it has helped so much. Thank you
N0 thank uou
The first thing that I want to learn about is not o
I had constipation, GI issues and "IBS "for 20+ years. I stopped using artificial sweeteners, chewing sugar free gum, etc. and my problems went away. I haven't had any problems since. It was artificial sweeteners.
i've had ibs for decades with zero artificial sweetners. now i drink coke zero and my gi issues are fine. not a definite correlation for all
I loved it ❤
I agree with pastorpresent1. Well explained, good volume and articulation. Lots of good information. I go to Duke and everything you spoke about is familiar. I experience these things often. Some even daily. Thanks for posting this . It goes along way in helping to understand what i experience.
Very informative really.
Small miningiena
T
The doctor is saying there is a probable connection between Irritable Bowel Syndrome and Parkinson's. If High Dose Thiamine Therapy ( as per Dr. Constantine) halts much progression of Parkinson's and Thiamine deficiency is very much related to the autonomic nervous system including symptoms of gastroparesis maybe the common connection is Thiamine.
I don't eat a lot of food. I can go 3 or 4 days easily without going to the bathroom. Since i am lactose intolerant i tend to eat a bowl of cereal or just drink a glass of milk to go.
I didn't know that a runny nose could be a symptom. My nose runs constantly. I also have had excessive drooling the past year when i sleep. Never thought about it being a symptom as well..
Should you be having a glass of milk if you are lactose intolerant?
@@Georgiaredfern I’m not sure but I think he’s saying if he takes milk it helps to make him ‘go’ to the toilet since he hadn’t had a ‘motion’ for days.
@@MargaretMcGill that's exactly it. My case is mild but milk, ice cream, cheese. It all makes me go to the bathroom.
Butter would help go, teaspoon or so a day. Olive oil too. The runny nose can be from the milk.
@@michiganmymichigan i only drink the milk when i haven't had a bowel movement in a while. I already take olive oil supplements as part of my healthy dietary regime. 👍
Thank you for discussing swallowing problems & how they can lead to weight loss. Living with PD, I try to keep nutrition drinks stocked for these times to substitute food bc I’m already underweight. I also try to drink Gatorade and extra water while dealing with no appetite times, trying to prevent more weight loss.
Mm
Crystal, you may also might try drinking a good quality Bone Broth (either buy at the store or make your own) as it has a TON of nutritional value that you may not be getting from Gatorade and it doesn't have sugar in it. Bone Broth has lots of protein
@@lisapizzale6466bone broth is great but for many with Parkinson’s, anything with animal protein affects the results of taking Levodopa. The meds won’t work because animal protein uses the same neurotransmitters as the dopamine. I can’t even have a small amount of dairy in my coffee. It’s so exhausting and tough to deal with.
My husband drinks milk at breakfast and dinner,usually 20ozs at a time. I have told him that I don't think he should be drinking that much milk. He likes his ice cream too! He is 82, what can I say ???
@@shmatalady5082😊
What do you think about Velvet Bean?
Irregardless is not a word. Use regardless or irrespective instead.
Vitamin B1 has been quite effective for Brain Fog. Melatonin has been equally effective for restless leg syndrome.
Theses don’t help me
B12
I have had day time drooling no control, gait, excessive, rigidity been diagnosed with RA and sjogrens but i couldnt lift my foot 1inch up just 6 years ago and now drooling, trouble swallowing all the time take days for food to get down
So informative and easy to understand 46:02
The best thing for the brain is what it's made of, fat and cholesterol.
Dr. Georgia Ede.
I have lower frontal brain disorder and wondering if that contributed to my Parkinson disorder
Alot of these symptoms are in Ms also
What about tired speech and not able to sing? Linda Ronstatt had to stop singing and I no longer can sing a note.
Wonderfull, I am so pleased to have been able to listen to this presentation. I am so convinced that I have Parkinson's disease. In 2009 I had an early diagnosis but was told I had Familial Essential by a N Tremor
Sorry the comment was not finished.
Iwas about to state by a Doctor of Neurological disorders. I am 86 now .
Me too! Can no longer sing.
This is my main problem too. Also I used to preach at church but can do so no longer.
I experience stuttering, stammering, and understanding some peoples speech.
Has patients being treated with carbonic/lepo been reporting increased incidence of external tooth deterioration? I submitted that question on the APA website and was shocked to get 500 positive responses in less than 24 hours.
I went for an acupuncture session and found I had so much energy. But today energy is less . Haven’t been diagnosed yet by a neurologist but have most of the early symptoms.
What do you do for a living? This common question if given unto its own fullness with all things being reconciled back to the father. The helping hand the loving hand and may only good love touch the works of your hands now and evermore.
Are there medications that help treat blepharospasm that doesn't involve botoxulin injections?
My mother had it and she smoked i saw her druel but she was medicated with depression meds she died of neumonia double they were trying to control her body temp they put ice cubes under her arms maybe for fever she fell alot she died she was on oxygen before she died
❤3.58
Not able to send my comments as send icon was not on.
4:02
3.58
Sorry, didn't mean to hit "down"
Lack of motility. My father had a saliva drool in his sleep. He used a patch of nylon cloth over his pillow to keep it dry.
I detest all these ads by Google!
Urinary urgency - also part of Alzheimer’s??
Constipation
Dr. Paul Mason: "From Fibre to the microbiome: Low carb gut health'
Caan you get this dease whith long haul covid?
no such thing - you mean cv vax injury
I have had to reduce my BP meds due to effect of levodopa on bp. (Lowers BP)
Ask about MELAS. IT is in our family, a very unknown disease, but many 😅 with it undiagnosed. Ask Google.
I would like them to start studying chronic akathisia. I got chronic akathisia from trying medications. I had no idea benzodiazepines could make you this incompatible with life. I have been left tortured alive 4 years off of Klonopin. When I got hurt, and it could be nothing else, I went looking for answers. I found 200,000+ hurt doctors, nurses and patients who had been screaming about this harm online if I’d only looked. Everything that makes akathisia feel better just down regulates you and makes you one notch worse. This iatrogenic harm needs screening before anyone else is hurt. Proper informed consent does not exist. Besides, how can you give informed consent for something so awful you cannot imagine it? How bad is your sleep? How depressed are you? Enough to be left tortured alive?
❤❤❤❤
Yes. I lost my singing voice and can’t stay on key. I am always flat!
❤ change you life still go only carnivor,eggs, butter no grain at all❤ se with happening you my feel better. Noting to lose 😊
fiddling with that paper clip thing is super distracting. tell me i'm not the only one this drives crazy LOL
I didn’t even notice it
I was not able to send the comments because send icon was inactive
I will send my comments later. I have saved the video.
Ask drs what the causes are.
She’s no dummy, thank you sweetheart.
And you arre rude, referring to this Doctor as sweetheart
It's 2023, and you never considered updating video + without 2015 clicking? wow, I tried.
The clicking distracted me too 😂
I get short of breath sometimes
Carnivor diet will help😊
If these patients have constipation, they should be fed better. Meat, fat, butter, more fatty foods and that will also feed their brains. Our brain is fat and cholesterol. Don't starve them......
Not enough attention has been given to failure or retorted ejaculation which also adds to ED.
Change you diet 😊
Hello
Disability isn't always visible.
Talk about tremors
Omg .great listening to this ,but wished you had stoped clicking the paper click in your hand . Lol ..
I do agree. Drove me crazy!!!
Maybe it makes her more comfortable with public speaking. Don't judge!
She may be changing slides in her Powerpoint presentation.
@@Dee-mj3puseems like nervous behavior.
Lucky me I have parkinsons and huntingtons in my family
So do I.
Parkinsons down the line in my family
I have blood pressure problems and I always hotter than my wife like that's an issue with her she can't stand the smell of old sweat on the bed and the couch and I have the shakes 3/4 of the time, the first time I was with my ex wife in '02. I also I had a major stroke in '99.
😅😅
Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms…My Dad is well again/
What medication?
@@danielletracyann it is a herbal medicine from Dr Madida
@@danielletracyann click and search #DrMadida
Please share the names of the medication that your dad used!!!!
What kind of medication did your dad take
Pills, pills, pills...
Sells, sells sells...
Again and again and again.
Oooh boy...if you only knew.😢
Allister begging sermon
Why isn’t she talking about diet?
Parkinson’s patients should be getting B1, the other B vitamins and plenty of healthy animal fat and protein. Your body cannot make cholesterol without animal fat. People on vegan diet end up with brain disorders in the long term.
She does mention increasing fiber and soft foods.
Most do not talk about diet.
She is a classic doctor.
She laughs about a serious issue…no good lady
Stop the clicking. So annoying. I couldn’t even listen to what she was saying. Idk why whoever uploaded this video didn’t notice this
I had to go back to even notice it. I hope that's you deliberating underscoring it and not over-sensitivity to sound
I did not notice that either
Didn't notice at all!
Did not notice clicking
I did not notice it until I read your comment! Now I am trying to tune it out by concentrating on her voice more. lol
The only word I can use about this video is, gross! Sure this was 2015 and it's now 2023 and we have seen a significant rise in Parkinson like symptoms and people that were tricked into receiving an unauthorized covid inoculation but are you kidding me, you still don't know some of the alternative therapies that can help prevent worsening symptoms? In fact you made a statement that, as patients symptoms progress, which means that the therapies you're using don't freaking work!
I treated pediatric patients and no more about treating Parkinson's than this speaker. That's a super sad statement.
Alternative therapies-Such as?
No more?? Know more. You're no doctor
Not interested in big pharma treating symptoms. Bye.
Parkinson disease 🦠 is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine that truly works that helped treat, cure and reversed all his symptoms. My Dad is well again.
What was the medicine?
Please share your information 🙏🏻
@@jennebeattie3168 Click and search #DrMadida
What was the medicine. Please share.
Was going to say there is no cure all medicine for Parkinsons unfortunately. Maybe her dad has some other problem that could be cured
Excellent presentation
hi I would like to know is it not safe to drive with pd