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First, I know I needed pin to banana connectors for mine (which is different than banana to pin connectors as those would not work for what I have since it is the electrodes that need the banana part)...but it could be that's what you already have and just typed it backwards. If not, though, it could be the problem. Pin to banana connectors were more difficult to find than banana to pin...at least when I was ordering them online. Second, if you don't have BOTH converters for both electrodes that could also be the problem. If one isn't connected properly it could cause an error. Third, make sure you have the right wires. I had to order the pin connector TENS wires because the ones that came with my unit were snap connectors and those won't work for tDCS treatments. You probably have the right ones but figured it was worth mentioning just in case. And last, I sometime will get an electrode error if I turn it on and one of the electrodes is not against my skin properly (not enough contact with my skin). This happened a number of times when I first started until I got the hang of it. Maybe since you are not doing the actual treatments yet this could be the problem. Not sure if that helps at all...but I gave it my best shot. :) |
tdcs and teenagers?
Hi I am new to this forum but have been reading the posts on tdcs with interest. My daughter was diagnosed the crps when she was 8 and with fibromyalgia at 13. She is now 15. I am wondering if there is anyone who has tried this treatment with a teenager and what kind of outcome they had.
Any information regarding this would be very much appreciated. I would also like to thank those who have posted on their experiences with tdcs, this information is very helpful. Marg |
Thank you
I appreciate your reply. I do remember that I got the TENS wires based on Ballerina's post. I believe I need some saline solution to put on the electrodes?
I just can't wait to get the pin to banana wire, you're right that's the one I ordered. I have a red one that connects to one electrode but not the black one (My mistake for not ordering both when I initially placed the order). As far as skin burns and such, I have a completely bald head and there's really no way to hide such burns. What preventive measures do you suggest I take to prevent burns? |
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So sorry your daughter has to face CRPS at such a young age. Her youth is in her favor though. I have not reviewed any clinical trials regarding tDCS and adolescents. As a start I suggest you give a call to Dr. James Fugedy in Atlanta one of the top tDCS docs in the country. If anyone knows the answer to your question he would. Dr. Fugedy runs a private tDCS treatment clinic for chronic forms of pain, including Fibro. I understand that Dr. Fugedy has had excellent success with Fibro patients. Since the treatment has been scientifically proven to be safe, is non-invasive and has a very low incidence of side effects, none of them serious, it would be a good thing to try if it is successful in adolescents. Hope this is helpful. |
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I got a standing ovation, clapping and many hugs when I walked in the room. I was nervous because I still have problems with balance, but that is improving. Yesterday I picked my nephew up from school for a dental appointment. After I signed him out at the office I waited in the hall for him. I could see him in the distance and as soon as he recognized me he screamed, Uncle Jimmy has no cane!" and came running to me. I hugged him with both arms, so thankful that the arm that was rendered useless by the Boston Scientific Spinal cord Stimulator is now totally back to normal. This weekend we are having a soft ball game in my backyard at the cook out my wife has planned to celebrate my new life. I plan to be in the outfield for a while and will maybe even throw a few pitches. I know you also struggle with balance issues, as do many others with CRPS. The balance issues were the last to start to improve for me. I still have them so I have to be very careful not to do more than I am capable of-you know how that goes. Three members of my support group are spending this week researching tDCS and balance issues. I will post what we find. It's odd how my feelings are changing. When I first started to respond to tDCS I was happy just to get out of the wheelchair. Then I was so excited just to be close to where I was prior to the implantation of the Spinal Cord Stimulator. Now that I am working to get off of the cane for good I want not only what the SCS took from me but I want it all now. I want the same thing for ALL others who have CRPS. I was thinking about you the other day in Walgreens where I saw some cool canes. I hope you have a pretty cane waiting by the door for your eventual graduation from the walker!!!!!!!!!!!!!!! How about hot pink with butterflies? Got to run to meet with the other two researchers. It is frustrating that we have to do this work ourselves but at least we have the tools to do it! Best to you and all who are using tDCS. |
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But seriously...I am so happy to hear all of this. I really hope that I have this to look forward to in my future. I have a pink walker and one of my canes is blue and the other black (both are the kind that fold up so I can take them with me in the walker if I have to). The blue one was a new purchase this past weekend...guess I didn't tell you guys about that. This past weekend my boyfriend had the weekend off (this never happens) so he told me Friday morning that he wanted us to go up his family's house on a lake in Wisconsin and go fishing. I was game...didn't look forward to the long drive for only two day but figured it would be alright because I have been feeling good lately. Talk about one of those trips where anything that COULD go wrong definitely tried to go wrong. One of the big things was that about 2 hours into the drive my boyfriend realized he didn't put my walker in the car and left it in the driveway at home...ugh! Rather than cancel the trip we called his mom who put the walker in our house and we bought me another cane at the 24 hours Walmart (because where else are you going to get a cane at 2am). So I had a day and a half with ONLY using the cane. It was awful. I am definitely not nearly ready for that. My pain was so much worse in my ankle and my right arm (the one holding the cane). Ever since we got back my ankle hasn't been quite the same...but I am hoping that with the tDCS treatments that it will get back in line soon. Oh well...good news is that I was actually able to go fishing and caught 35 fish in the 7 hours total that we spent on the water between the two days. Had to alter my fishing technique a little bit because of the RSD but I made it work. It hurt but I'm sure you know what it means to be able to do something you enjoy despite the pain. Definitely have to wear gloves because not a chance I could touch the cold fish to take them off the hook without causing a flare. Oh well...I'll take what I can get. So yeah...not ready to go without the walker yet...but hopefully some day. Just hope I didn't set myself back too bad with the walking with just a cane for a day and a half. It wasn't much walking but it was the hill and uneven ground to get down to the pier that did it more anything else I think. I am also VERY wobbly on the cane still. I guess it's easy to take the walker for granted and how much it really helps until you really don't have it at all. You just be careful with that baseball...would hate for you to have another injury. I used to be a pitcher and I got clocked a number of times on the mound when pitching...not much time to react there if something comes back at you. But definitely enjoy yourself at the party...you deserve it! |
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" Wow" thirty five fish in seven hours thats pretty good fishing. :hug:Joydee |
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Tdcs
Hi,
Just wanted to let those with interests in TDCS know we have at last been able to re-set the date for my daughter to consult with Doc Fugedy in Atlatna on June 2, 2012. My husband will book the flight for the two of them. :)Joydee |
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