Kim you are amazing....getting right to what you can do and doing it. It makes me realize that I spend too much time being angry. This is a great lesson.
I was diagnosed last May at 75 yrs. of age. Your story is similar in some ways to mine. Being diagnosed during this pandemic has made it a bit more challenging. Look forward to hearing more of your story.
Hi Kim. I too have PD. Thank you! Looking forward to seeing more of you. I'm at stage 3. As you know there are 5 stages. My body changes have been disappointing of what I had envisioned my older years were going to be like. I'm 68. I also have epilepsy since age 13. Unfortunately, they always chalked my symptoms up to that. My dad had PD and I was told for years it wasn't hereditary which wasn't true. I feel I've had it for about 15-20 years now. I look forward to hearing more from you all. GBU.
I am on a journey to find out ifbi have parkinson's. I started getting symptoms 3 years ago and have seen over 15 doctors. Along they way they found a tumor in my head that was removed but I continued to get much worse. My symptoms are severe muscle pain in my neck/shoulders and face as well as migraines, very stiff and no right arm swing, slight resting tremor in my right hand, lots of visual issues and dry eyes, I yell in my sleep as well as sleep apnea, drag my right foot, cognitive issues, sweat like crazy but freezing and lots of nausea, I feel like I am wearing a band around my mid section. I have been seeing a neurologist who thinks I have a leak in my spinal cord but also said I show the signs of parkinsonism/parkinson's. I haven't loss my smell and my hand writing is still pretty good but right hand is so unpredictable and I drop things or can't close my hand when I want. I also suffer from the depression and anxiety. Cry a lot for no reason. Not asking for your diagnosis but just wondering if you have similar symptoms and issues? I'm 55. I also have cogwheel in my right arm and wrist as well as hyperaflexia.
Sorry for what you’re going through. I’ve had some similar symptoms but your situation sounds more complicated. I would suggest seeing a movement disorder specialist if possible - this is a specialized neurologist who could give you a more definitive diagnosis.
KIm thanks for being so brave. I glad that you have shared this with the world. Becuse of this video I have a better understand of what you are going through. I hope there is more to come. Robert
Agreed. I have been low carb for 2.5 years and diagnosed with PD for 1.5 years. I feel this way of eating is the best and has helped my overall health.
I’m so glad I found your podcast I’m 54 and just got diagnosed in January. I have been feeling very lonely and scared you give me hope thank you.
I am diagnosed this year
You are truly an inspiration of hope and action... love you, Kim!! 🌷
Kim you are amazing....getting right to what you can do and doing it. It makes me realize that I spend too much time being angry. This is a great lesson.
I was diagnosed last May at 75 yrs. of age. Your story is similar in some ways to mine. Being diagnosed during this pandemic has made it a bit more challenging. Look forward to hearing more of your story.
Thank you. I was diagnosed with Parkinson"s five years ago.
Hi Kim. I too have PD. Thank you! Looking forward to seeing more of you. I'm at stage 3. As you know there are 5 stages. My body changes have been disappointing of what I had envisioned my older years were going to be like. I'm 68. I also have epilepsy since age 13. Unfortunately, they always chalked my symptoms up to that. My dad had PD and I was told for years it wasn't hereditary which wasn't true. I feel I've had it for about 15-20 years now. I look forward to hearing more from you all. GBU.
I am on a journey to find out ifbi have parkinson's. I started getting symptoms 3 years ago and have seen over 15 doctors. Along they way they found a tumor in my head that was removed but I continued to get much worse. My symptoms are severe muscle pain in my neck/shoulders and face as well as migraines, very stiff and no right arm swing, slight resting tremor in my right hand, lots of visual issues and dry eyes, I yell in my sleep as well as sleep apnea, drag my right foot, cognitive issues, sweat like crazy but freezing and lots of nausea, I feel like I am wearing a band around my mid section. I have been seeing a neurologist who thinks I have a leak in my spinal cord but also said I show the signs of parkinsonism/parkinson's. I haven't loss my smell and my hand writing is still pretty good but right hand is so unpredictable and I drop things or can't close my hand when I want. I also suffer from the depression and anxiety. Cry a lot for no reason. Not asking for your diagnosis but just wondering if you have similar symptoms and issues? I'm 55. I also have cogwheel in my right arm and wrist as well as hyperaflexia.
Sorry for what you’re going through. I’ve had some similar symptoms but your situation sounds more complicated. I would suggest seeing a movement disorder specialist if possible - this is a specialized neurologist who could give you a more definitive diagnosis.
Please don’t iu 1:10
KIm thanks for being so brave. I glad that you have shared this with the world. Becuse of this video I have a better understand of what you are going through. I hope there is more to come. Robert
Please try carnivore diet. Look up Dr. Ken Berry.
Agreed. I have been low carb for 2.5 years and diagnosed with PD for 1.5 years.
I feel this way of eating is the best and has helped my overall health.