Update on my DRG stimulator Implant. Implanted 12 days ago.
Hi all my fellow Neuropathy Warriors, Just wanted to update you on this DRG stimulator in me. Basically, so far, not so good. It seems to help pain in the morning, pain from a 9-10, to about a 5-6, maybe a 4, at times. As the day goes on, pain gets worse. Nights are still bad. Yesterday was the first time I walked outside. I walked around the block twice, and it was wonderful to smell fresh air, use my legs, etc. However, when I came back into my house, I felt like my feet were on fire for a few hours. Another thing that I have noticed in general, is foot exhaustion. Sometimes I feel like I have ran a 35 mile marathon, and that I need endless foot massage. All in all, so far, not real good. Going to my pain doc tomorrow and will also meet my ABBOTT rep there. In hindsight, I really wish I had more good days during the trial of my DRG. I had only 3 improved days; days 7-10, and then, the doc had to remove the DRG due to risk of infection. I wish I had more good sample days!!! I am praying, of course, as my nerves in the lumbar DRG area heal, I will improve. So far, not really worth doing. Saddens me beyond belief. Thank God for Kratom. I just sent my Kratom company a "love letter." I do not know what I would do without that product, and may advocate for Kratom. What the hell! Gotta put my energy into something positive!!! Maybe some chocolate chip icecream, too. Love to each of you, Lori Renee
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Hi Rachel, not sure if you are on your trip to the cabin already but I was wondering about your mention of using heated seats for you back/legs in the car. Does the heat help the pain? Is it therapeutic as well, i.e. does it improve the back/leg issues as also? Or does it simply help you to keep your muscles warm and therefore more comfortable? Might seem like a dumb question but I found your mention of it interesting to me.
If you ARE on your trip I hope you are having a great time! Best, Hank
@jesfactsmon My trip is next weekend Hank. For me, heat settles the pain temporarily. Probably by warming the muscles and keeping them from tightening due to defective nerve function around them. I find heat to be my savior most days. My calves, thighs and knees suffer from terrible aching, burning and muscle pain so I wrap my legs a lot. My back and hips experience the same, plus tightening and spasm, and heat is a great help. It's used each week by my PT before he performs myofacial release therapy.
Whoa. Unbelievable, your leg situation. And you think this all triggered from a b12 deficiency? Forgive me for asking if you've already said this before, but I am wondering if anyone else you are related to has anything similar to what you have? It's weird how this crops up. Linda has no one in her family that has anything like her health issues. It's strange.
Nope. My father is diabetic, that's all
Apparently, yes, B12 deficiency. I believe it was caught way to late.
Hi Rachel, i want to wish you a lovely trip next week and hope the magnesium will help. I often get leg cramps and creepy crawly feeling in my legs at night despite taking magnesium pills. I use a magnesium cream which works well and have also used the Hylands leg cramp pills which sometimes work on the jittery feelings. With regard to genetics, I thought I remember your mentioning your Mother having a chronic pain problem in the past which might shed some light on your current issues? It seems to me to be very unusual for just a vit. B deficiency to have gone undetected for so long as to cause such extreme health issues, I would not have been happy with my family care physician for having missed this. Helen
@helennicola Hi Helen. You are too sweet! Thank you for your advice, inquiry to my health and well wishes for my trip. Yes, my Mother had a motorcycle accident in 1978, broke both legs and has endured chronic pain ever since. While going through extensive testing to find an underlying cause to my Small Fiber Polyeuropathy diagnosis, genetic testing was performed. It concluded as unremarkable. I do know my migraines are hereditary as well as my cornea disease. As far as how my body has handled disruptions and became chronic....my thoughts are Chronic Pain Sensitization which maybe my neurologist will conclude in August when I see him, or, Mayo will have some revelation in October at the pain clinic. Til then, such is life. I try hard to remain optimistic and you folks here on Connect have been a huge help and inspiration to me. I cant thank everyone enough. 💕
@rwinney You think the burning achy legs are from B12 defiency Mine started after my fracture in 05 but has gradually gotten worse. I,LL have to mention this to my Dr It's only my thighs but heat does help I just use a heating pad
Good afternoon @lorirenee1. I just read your post a few times to make sure it actually said what I wanted to see. I can just invision beginning to have freedom from discomfort and pain. And the walking, the fresh air. Enjoy every moment.
I also wanted to tell you that you have mentioned an issue that I have noticed with my practitioners and clinicians, they do not tell you everything you really need to know about a treatment or medication before you make a decision. The best decisions are made by folks who have the most information about the choices. Those of us who work hard to become our own advocates seem to do pretty well. Keep up the good work and the good news.
May you feel joy today.
Chris
Rachel @rwinney I hope your trip to the cabin is still on for this weekend. I want to wish you the very best time possible with your family and I hope you have not just a tolerable drive up but a NICE one. You, my friend, deserve it!!!!!! All my best, and with love, Hank