Parkinson's Disease Tulip


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Old 11-16-2014, 12:40 AM #11
Betsy859 Betsy859 is offline
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Betsy859 Betsy859 is offline
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Originally Posted by made it up View Post
Hi again Betsy,
There has been peer reviewed findings in recent yrs that DBS done early rather than later in the course of PD has been beneficial.
I have a full drivers licence and still drive. I do most things like before.
Cook, shop, laundry etc.
I cycle on a stationary bike in the cooler months and now that its warming up here I exercise in the pool.
I've had PD formally diagnosed for 20 yrs now and was in my mid 30's when told I had it.
I know the PD has progressed but only because my neurostimulators or IPG's (internal pulse generators) as the batteries are known as both went completely flat on me 2 yrs ago and the few days without them were awful!
My Sinemet dosage soared and i had episodes where I couldn't move any part of me but could still speak so had my husband put Sinemet in my mouth as I couldn't.
Feeling so unwell and dependant really made me grateful for the independence that I enjoy on an everyday basis now and the realisation that without DBS in my case anyway I would have to depend on others so much.
In the early days after DBS was first done I managed without any meds at all but thats not very common and in retrospect I should've or could've taken a little but chose not too.
I take it on a regular basis now and have had no further recurrence of the dreaded dyskinesia which was bad before DBS.
Bradykinesia is minimal too, now when off its more a feeling of rigidity.
If you need further info there are websites like yahoo DBS that have many knowledgeable recipients of DBS that i think would be glad to help as well.
Best wishes.
Thank you so much for your incredible story. And thank goodness for DBS to help with this disease. it just takes the courage to do the procedure. I'm starting to look into hospitals and fortunately Im close to some very reputable places. I know research suggests DBS should be done early but when one's PD is fairly well under control as mine is at this time it's hard to get this procedure done.
I hope all continues well for you and will post any action I take regarding DBS.
All the best ,
Betsy
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Old 11-16-2014, 01:06 AM #12
Betsy859 Betsy859 is offline
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Betsy859 Betsy859 is offline
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Originally Posted by damon4309 View Post
Hi Betsy
Weight gain in DBS is probably different degrees . Mine seem to have leveled off. I am stuck with 229s lbs. My MDS stated 3 to 6 months and it may become stable. Prior to surgery I was to busy worrying about walking and symptoms of
caused by the meds mainly paranoia. Not being able to walk burns calories as do dyskinesias . After DBS there is constant stimulation where the metabolition
becomes stable probably lower. I am not sure what caused the excessive appetite but I have it under control. I try to eat healthy while watching calories
I use the nutribullet for veggies and fruit. I was scared to have DBS. It really is not as bad as it sounds. It does not hurt (mild discomfort). I am due on Dec 18 for my 4th programing. I have only "on" time. The ability to drive has been renewed. The only discomfort is a heavy feeling in my legs which will be targeted at the next programing. The meds have been reduced by about 40%. Congrats on your daughters 25th birthday. To sum it up, when the ability to take care of yourself is gone and the meds stop working as they use to, DBS will enhance
your quality of life.

Hi Damon,
All sounds good I've been cheering you on from afar! Thank you for that info on the BDS procedure being fairly "mild" that's encouraging. How often are you getting programmed? And do you go back to the hospital or to a doctor's office? IF I do this Im thinking about the procedure being done at Hopkins but it's 75 minutes away so was wondering about the programming. But all that will be covered by the hospital when I get screened to see if I even qualify for the procedure. One of my neurologists is encouraging the procedure because of my resistant tremor and my intolerance for these meds. At this point I'm going to enjoy the holidays and worry about it in the new year. I see the neurologist Tuesday so will talk to her more at that time.
Are you sleeping better? I used to sleep like a baby until PD. Now I can't sleep at all and often have to take naps during the day. I take a 3mg melatonin every night. Don't really want to start on anything stronger at this time.
Good luck with your next programming and continuing diet. It makes sense that appetite levels out after your body adjusts to the DBS.
Good luck and all the best,
Betsy
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Old 11-16-2014, 03:53 PM #13
damon4309 damon4309 is offline
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Default DBS and weight gain

Quote:
Originally Posted by made it up View Post
Hi again Betsy,
There has been peer reviewed findings in recent yrs that DBS done early rather than later in the course of PD has been beneficial.
I have a full drivers licence and still drive. I do most things like before.
Cook, shop, laundry etc.
I cycle on a stationary bike in the cooler months and now that its warming up here I exercise in the pool.
I've had PD formally diagnosed for 20 yrs now and was in my mid 30's when told I had it.
I know the PD has progressed but only because my neurostimulators or IPG's (internal pulse generators) as the batteries are known as both went completely flat on me 2 yrs ago and the few days without them were awful!
My Sinemet dosage soared and i had episodes where I couldn't move any part of me but could still speak so had my husband put Sinemet in my mouth as I couldn't.
Feeling so unwell and dependant really made me grateful for the independence that I enjoy on an everyday basis now and the realisation that without DBS in my case anyway I would have to depend on others so much.
In the early days after DBS was first done I managed without any meds at all but thats not very common and in retrospect I should've or could've taken a little but chose not too.
I take it on a regular basis now and have had no further recurrence of the dreaded dyskinesia which was bad before DBS.
Bradykinesia is minimal too, now when off its more a feeling of rigidity.
If you need further info there are websites like yahoo DBS that have many knowledgeable recipients of DBS that i think would be glad to help as well.
Best wishes.
Hi Made it up and Betsy
I recently was told that the stimulators were good for 2 to 5 years and that they were able to tell when a patient was needing a replacement. I imaging it was terrible for the couple of days that you were without them. How long had they worked before going flat? It makes sense that the lack of dysconesias would lower the metabolism but doesn't explain being hungry all the time. I can't post the link because I a new but I found a really good article on PD in general. JUst google PennStateHershey Parkinsons Disease. The article pretty much covers a lot of questions. I have ordered Forskolin Extract standardized at 20%. This is for weight loss and should not interfere with any PD or DBS benefits. It is not a stimulant but a supplement for weight loss. Normally I would not believe in this but I first heard of it on the DR Oz show. Anyway I will be getting it from Amazon this weeks and let the forum know if I feel any different and what effect ,if any, it has on body fat.
Have a great week!
Damon
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Old 11-16-2014, 04:31 PM #14
damon4309 damon4309 is offline
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Quote:
Originally Posted by damon4309 View Post
Hi Made it up and Betsy
I recently was told that the stimulators were good for 2 to 5 years and that they were able to tell when a patient was needing a replacement. I imaging it was terrible for the couple of days that you were without them. How long had they worked before going flat? It makes sense that the lack of dysconesias would lower the metabolism but doesn't explain being hungry all the time. I can't post the link because I a new but I found a really good article on PD in general. JUst google PennStateHershey Parkinsons Disease. The article pretty much covers a lot of questions. I have ordered Forskolin Extract standardized at 20%. This is for weight loss and should not interfere with any PD or DBS benefits. It is not a stimulant but a supplement for weight loss. Normally I would not believe in this but I first heard of it on the DR Oz show. Anyway I will be getting it from Amazon this weeks and let the forum know if I feel any different and what effect ,if any, it has on body fat.
Have a great week!
Damon
http://pennstatehershey.adam.com/con...=10&gid=000051
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Old 11-16-2014, 08:30 PM #15
made it up made it up is offline
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made it up made it up is offline
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Quote:
Originally Posted by damon4309 View Post
Hi Made it up and Betsy
I recently was told that the stimulators were good for 2 to 5 years and that they were able to tell when a patient was needing a replacement. I imaging it was terrible for the couple of days that you were without them. How long had they worked before going flat? It makes sense that the lack of dysconesias would lower the metabolism but doesn't explain being hungry all the time. I can't post the link because I a new but I found a really good article on PD in general. JUst google PennStateHershey Parkinsons Disease. The article pretty much covers a lot of questions. I have ordered Forskolin Extract standardized at 20%. This is for weight loss and should not interfere with any PD or DBS benefits. It is not a stimulant but a supplement for weight loss. Normally I would not believe in this but I first heard of it on the DR Oz show. Anyway I will be getting it from Amazon this weeks and let the forum know if I feel any different and what effect ,if any, it has on body fat.
Have a great week!
Damon
Hi Damon and Betsy,
When it was time for my IPG's to be changed after the first wore down the warning light blinked as it was meant to on my patient programmer warning me in my case that one side was showing it was wearing out and so they were both changed at 3 yrs and 11 months.
The second time they needed replacing the warning didn't come on my programmer and then they both showed that they'd both gone completely flat after 4 yrs and 8 months.
I now have a newer programmer (I'm sure yours is same) that Ive been told is more accurate at warning of battery life wearing down plus I really like that I can change my settings up or down a little.
I check it at the start of each month for it to flash so next time I'll have some warning hopefully!
Betsy, I think one of the criteria for DBS is that meds are causing you to have unpredictable offs so it may be some time before you would be classified as a suitable candidate.
That plus I think personally you have to really want it yourself because you feel your own quality of life could improve with it.
Best wishes to you both.
Lee
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Old 11-17-2014, 01:01 AM #16
Betsy859 Betsy859 is offline
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Join Date: Jul 2013
Location: Maryland
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10 yr Member
Betsy859 Betsy859 is offline
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Join Date: Jul 2013
Location: Maryland
Posts: 38
10 yr Member
Default

Quote:
Originally Posted by damon4309 View Post
Hi Betsy
Weight gain in DBS is probably different degrees . Mine seem to have leveled off. I am stuck with 229s lbs. My MDS stated 3 to 6 months and it may become stable. Prior to surgery I was to busy worrying about walking and symptoms of
caused by the meds mainly paranoia. Not being able to walk burns calories as do dyskinesias . After DBS there is constant stimulation where the metabolition
becomes stable probably lower. I am not sure what caused the excessive appetite but I have it under control. I try to eat healthy while watching calories
I use the nutribullet for veggies and fruit. I was scared to have DBS. It really is not as bad as it sounds. It does not hurt (mild discomfort). I am due on Dec 18 for my 4th programing. I have only "on" time. The ability to drive has been renewed. The only discomfort is a heavy feeling in my legs which will be targeted at the next programing. The meds have been reduced by about 40%. Congrats on your daughters 25th birthday. To sum it up, when the ability to take care of yourself is gone and the meds stop working as they use to, DBS will enhance your quality of life.
Hi Damon,

So glad that things appear to be heading in the right direction. What a relief this DBS has been for you. Good luck in your next programing. How often does the programing occur; does it differ from person to person? Thank you for the procedure information glad there's no pain, of course. I'll see my neurologist Tuesday and discuss DBS further. It's hard to consider doing such an invasive procedure when my PD seems under control as least at the moment. Meds are taking a toll on me even at low doses. That's why I'm considering the procedure and then the possibility that stem cells might be stimulated to grow.
Right now I'm going to concentrate on the holidays and not worry about DBS until after the new year. Btw does Medicare pay for this procedure or is the expense out of pocket?

All the best to you. Keep me posted how your programing is going.
Betsy
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