I had my FUS treatment two days ago at Sonimodul and although it wasn’t easy with a full on dyskinesia attack I really enjoyed the sonications where I knew my brain was being fixed. My left side is symptom free now and I can walk. Thoroughly recommended. The team there are incredible and I felt my brain was in good hands. They said the procedure went really well and for the first time in 20 years I feel much closer to ‘normal ‘ neurologically.
Focused Ultrasound : I had my FUS treatment... - Cure Parkinson's
Focused Ultrasound
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So pleased to hear yet another surgery success story! Whether it's FUS or DBS, surgery is the one thing that is here and now with the potential to really move the dial on the quality of life front.
Unless I'm wrong, you were a bit nervous that you may have waited too late. Seems those concerns are now no longer?
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No, I don’t think there’s such a thing as too late unless dementia has set in.
Congratulations! Looking forward to reading more when you are feeling expansive. Didn’t you have to be unmedicated for the procedure (for the previous 12 or so hours)?
At last, you got your turn. Thank you again for bringing the FUS PTT info here at HU.
To the non tremor dominant members, who's quality of life is usually worse than tremor dominant, there is hope!
So happy for you !!!
Very good news. I sent my files yesterday and I plan to do it next year.
So, I sent my files yesterday and today David Moser already replied with dr. Jeanmonod in the CC line telling me next week the doctor will study my files and he will give an answer.
They are reacting pretty fast. David asked me if when I did the videos I was taking the medication which helps just a little with my tremor.
I replied I was taking medication when I shot the videos and David wrote back to shoot another set of videos being 24 hours drug free. The last pill I took was at 4.30 pm Friday US EST. I'll shoot the videos today at 4.30 pm.
For few months I was waking at 3 am every night so I had to take a c/l pill or/and 10g melatonin to get asleep again. Last night I slept continuous for 9 hours without any pills.
The cost?
34k Swiss francs
Hi, all the best to you. I have one question about tretman price,is it 34 k just for one side or both included.
34k for one side. You might not need the other side doing. I don’t feel like I do at the moment and I’ve had symptoms on both sides for about 12 years.
What were your main symptoms? How does FUS affect gait improvement? Thank you.
My gait was bad because I had dystonia in my left leg which twisted it inwards and I could only walk on the outside of that foot. I’m still taking medication and if I don’t I shuffle with my untreated side. My main symptoms were dystonia, dyskinesia, rigidity, bradykinesia. Now when I take Sinemet I feel totally normal except for a bit of fatigue and ADHD symptoms. Since the motor symptoms have improved so much I’m more aware of my cognitive symptoms.
Thank you very much for sharing your story and congratulations! I will be following you, Lena, Marc, and anyone else who has undergone PTT with great interest. I am inspired by your courage and soooooo encouraged by your success!
Excellent news
So pleased for you. Must feel great after all that you've been through?
Yay! Thanks for sharing.
Is there a difference between FUS done in Switzerland compared to in the U.K. or US? I’ve seen FUS carried out on PD patients in both (& in Israel). And so wonder why people go to Switzerland particularly?
Seems the Swiss are the only ones doing the PTT commercially at the moment.
"pallidothalamic tractotomy (PTT), has been performed since 2011 using the MR-guided focused ultrasound (MRgFUS) technique"
My understanding, which is limited, is that the PTT procedure offers a broader range of symptom relief than what is offered elsewhere (at the moment).
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PTT is the only form of FUS that can be perform both sides of the brain. So for someone like me who has symptoms on both sides it’s the best option. Also Dr Jeanmonod has way more experience than anyone else in the world.
Hi Trixiedee. I am scheduled for mid November. Nice to know yours went well. Yes, the team are great!
Parkygal
Incredible news! Great that the procedure went well.. How long did it take? keep us posted!
Can you turn over easier in bed and is your speach better than prior the surgery? (If you had these symptoms before)
Thank you
Yes I can turn over in bed and my speech is stronger. I really struggled to turn over in bed before.
That is so good to know. I have had a hard time turning in bed since the very beginning of symptoms. It got a little harder each time I had to decrease c/l because of side effects. By now, my husband has to move me in bed... I feel like a beached whale... As far as speech, my husband is about the only one who understands me by now: "off" meds stiff jaw, tongue and lips, "on" meds jaw dystonia (different difficulty, no more easy to understand)... Very soft voice on and off... Looking forward to Feb. Also, can't wait to take a waĺk like you did: it's been such a long time...
So happy for you! Every hope realized is a victory.
Does it matter what stage of the disease you’re in? Presently, only my right side is effected.
Did you have movement problems no tremor non-tremor dominant. The procedure is it removes or destroys an area of the brain- for tremor the procedure is different.
I researched the surgery called a Pallidotomy this was performed more than 50 years ago but not done because it was to difficult only a few Doctors would perform the operation. The results for a successful surgery were very good.
The pharmaceutical industry created the need for drugs that are not successful and very damaging.
FUS is still used mostly for tremor my guess is the pharmaceutical industry does want to cure people not enough money to be made.
I tried getting FUS for my wife years ago but she did not have tremor and $38,000 we did not have.
Great to hear that someone was helped sadly this procedure should not cost $38,000 and should be available at a reasonable price.
So , I’m confused. This procedure works for tremor dominant, or non tremor dominant, or both types? Thank you.
Finally. Your perseverance paid off. A lesson for all of us. So happy for you. Enjoy your new life!!
That is wonderful news! Congratulations!
After I sent my medical reports and two sets of videos (on medication and 24 hours off medication) dr. Jeanmonod just emailed me today asking for a phone conversation for next week.
I'm just curios if you went through the same steps.
Thank you.
Wonderful news Trixiedee! 👏👏👏
So good to hear your great news Trixiedee! The the first time, when you were turned down because you lacked a support system for recovery, we were feeling so bad for you. At that time, we were anxiously awaiting to hear back from them after sending in videos. When we did hear back, our experience was heartbreaking.
Here's what they said:
"The clinical state of Mr. ___ displays as main problem a gait disorder, which requires a bilateral treatment with two interventions separated by a year. In forms with akinesia and rigidity but without typical tremor, as is the case for him, the results are mixed, with improvements but also worsenings, due to brain reserve reduction and psycho-emotional load. The chances of satisfactory relief would thus be low. A sufficient general and neurological health state is also important to stand a long therapeutic program out of the USA."
This was really our last hope. Wondering if it might be worth it to approach them again with new videos. Any thoughts?
Trixie, fantastic news! I am so happy for you and anyone who had a successful FUS operation. Please keep up posted!
Do you still have to take meds? If so, I imagine a lot less now.
So happy to hear you've had a good outcome! Thank you for sharing your story!