DBS: I have had DBS on Nov 201... - Cure Parkinson's

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DBS

SuKas profile image
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I have had DBS on Nov 2012,...... inspite of several tuning sessions unable to find the "sweet" spot.... frustrated

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SuKas
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14 Replies
compucure profile image
compucure

I guess that each of those of us who have had DBS will more than likely have a different story to tell. I thought I had found the sweet spot, but recently have experienced a significant increase in tremor and rigidity - it has suddenly crept up on me. Tony

SuKas profile image
SuKas in reply tocompucure

Tony...very true...all of us diff experiences....was frustrated as we were going nowhere fast...but i think the problem may have been rectified...changed the programmer...sorry to hear about the tremors and rigidity....that is exactly my prob

professor profile image
professor

WELL THERE ARE SEVERAL SITES THE PROBE CAN GO

EACH PROVIDE DIFFERENT EFFECT, DEPENDING ONTHEIR INTERPRETATION OFYOUR SYMPTOMS THEY CALCULATE POSITION , SEEK SECOND OPINION

SuKas profile image
SuKas in reply toprofessor

Professor, u are right... changed the programmer....keeping fingers crossed:)

Jash profile image
Jash

It takes a long time, perseverance, and an excellent programmer. I changed programmers and that made a huge difference for me.

SuKas profile image
SuKas in reply toJash

Jash, u are so right...i changed mine too...lets see:)

98Rob profile image
98Rob

Jash is right. Remember that it may take some time. A good programmer is crucial. How often do you go for a "Tune up"? I felt immediate relief when my DBS was turned on in Feb. 2007. But it took about a year of going every three months. for adjustments to truly take effect. I am going this Thurs. for my first "tune up" in 6 months. I have very little I need the doctor to make major changes this time. I've also had adjustments thru the years where I've had to go back earlier than my next appt. which is usually every 4 months. Also keep in mind that DBS is not a cure. You will have to continue to take medication as well. PD is a progressive disease. Which means it is always getting worse. Thus the need for tune ups several times a year. Where do you live and what are your options for programmers? Don't get frustrated. Stay strong!!

SuKas profile image
SuKas in reply to98Rob

98Rob, Thank u much for ur encouraging reply. as this is my first year, i am going every three months...have had several programmers, but now the doc has taken over so shud be good

Jash profile image
Jash in reply toSuKas

Not only does it take time for your brain to heal and adjust, but your whole body is in a new suit and alterations are necessary. After about a year, I got an excellent bloodwork report from my doc. Said it was consistent with my "younger" self. I thought they had just mixed up the labs. But my PCP said he's seen this many times when people with chronic diseases get them under contralt and managed well ( like diabetes for example) that overall health improves. Good luck. May the best possible outcome be yours

SuKas profile image
SuKas in reply toJash

true though..yes it does take time for ur brain n body to heal...luckily otherwise my health is ok other than hypo thyroid

Jeanna profile image
Jeanna

I had my DBS surgery in Jan 2013. I am still undergoing programming sessions about every 3 months. I have had a decrease in tremors and internal feelings of tremor but I am very slow moving and don't move my left foot well in the evening. I also become very stiff and have a lot of back pain and rt hip pain. I don't know if these are Parkinson's related or arthritis. I too feel frustrated.

SuKas profile image
SuKas in reply toJeanna

oh sorry to hear that, yes we do tend to attribute most of our aches to PD..Hope u feel better

Cookie1124 profile image
Cookie1124 in reply toJeanna

Did you have the awake or asleep DBS?

SuKas profile image
SuKas

I am sorry I disappeared after posting this....was having my meds titrated after a tuning, and my body is sensitive...we may have reached the right cocktail mix so to speak:) Thank u for ur responses.

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