Spinal Cord Stimulator
Posted , 146 users are following.
Has anyone had a spinal cord stimulator,it has been one suggestion for my husband who is still suffering after 4 years after his first surgery, he has had a further op two years ago and is still suffering immense pain, has weakness in his leg and finds walking difficult and now needs a stick to walk with. I am hoping someone has had a spinal cord stimulator that has had similar condition as my husband because as I understand it it is only a minor op to implant. I think the other option is fusion which I have heard horror stories about, especially as he doesn't seem to have success with major ops. Thanks
19 likes, 888 replies
michael11297 khi
Posted
I am 2 weeks post op on my permanent SCS. I still have lots of surgical pain, especially where the battery is located. They turned my unit on about 1 week ago and I have no more nerve pain. I was involved in a rear-end collision about 2 years ago and developed permanent nerve damage in 3 spots between my neck and right hand. I have 2 leads and they are both thankfully working. I am still trying to get sleep patterns fixed and dealing with a little nausea but I'll take that over the nerve pain any day. How are you doing?
kilee michael11297
Posted
I just had the permanent one inserted abt 15 hours ago.YES I'M HURTING RIGHT NOW.
Kilee
michael11297 kilee
Posted
I have Medtronics
Hang in there the surgical pain does get better
I am now 6weeks post op and only have a little pain from the battery location. I used lots of ice in the beginning and my bruises faded quickly
The amazing payoff for me is sleeping through the night and no nerve pain
Good luck
Michael
lindagkelly kilee
Posted
I'm sure you are in a lot of surgical pain right now. I think the more surgeries we have, the harder it is to recover. I remember after I had my last Medtronic implant, I was calling the poor nurse in there constantly. The only thing that saved me was that I brought my own pain meds from home which I was taking at the same time as what they gave me! It's rough I know. Just do everything you can to distract yourself. At least you are able to get on the computer and talk to people. Please keep posting. I sure hope this gives you the long term relief you are looking for.
Linda
mas543 kilee
Posted
Mel
kilee mas543
Posted
kilee mas543
Posted
mas543 kilee
Posted
I have my first appt. to get this started next Thursday with the Pain Physchologist, for the insurance company.
Mel
mas543
Posted
Thanks all,
Mas543
glxpassat kilee
Posted
lindagkelly khi
Posted
lindagkelly khi
Posted
Top 3 Exercises For Herniated Discs
*All of these help with leg pain.
Prone Prop – lay on stomach propped up on elbows or on a pillow for 2 minutes
Prone Pressup – lay on stomach – prop up on your hands and push up
Standing back bend. Put your hands on the back of your waist, and bend backwards, or you can press against the wall.
I'm going to try them. Good luck all
april_pain_1 khi
Posted
I should mention I'm allergic to Ibuprofen, which means I can't take ANY anti inflammatories,(anyone with pain knows this SUCKS as no matter the amount of strength of pain medication, it won't touch the pain as most pain is due to inflammation)!
Anyway, I can no longer take anything with acetaminophen as my body has stopped banning it down so I'm on a regiment of 40mg ER Oxycontin, I take one I the am & 1 in the pm, I have 10mg Opana that I can use for pain throughout the day, (basically as some would take Advil etc.), I also get Radio Frequency, nerve ablation injections,(they are supposed to be dine every twelve months, I'm lucky if I make it to 6 months however the absolute soonest they can do is every 8 months).
I am a hair stylist who now can only handle 15-20hrs, I love what I do & therefore I'm unwilling to give up plus in only 45. I've fought disability & like my pain Dr says they aren't in the biz of helping patients go backwards, hence disability they are there to help feet better.
So this is where the HF10 has been introduced... I'm trying to get as much add info as possible as with my job I'm at a family owned company that doesn't offer ANY benefits such as FMLA, basically if I don't work I don't get paid! So when the Dr tells me due to my physical job I'm looking at 6 weeks recovery when the permanent device is placed.
I first apologize for the length of my message. I however have a few questions that I'm hoping one or more of you may know answers to.
I've heard that you can go on disability & still work 15+ hours so long as you earn less than they allow, (which I'm sure I'd meet the salary requirements.
I don't want to go on but disability but can't afford to get the care I need if I didn't as I don't get sick time, vacation, NOTHING. If I don't work I don't get paid period!
My other concern is had anyone had this device implanted for quite a substantial amount of time & had it worked?
I just feel lost depressed & at wits end. I try to stay up beat I'm always smiling at work, my clients are amazed wedge they find out as they tell me, I'm always so up beat, always smiling, etc. which is true because I love my job & well I'm actually working I don't even think of the pain, it's afterward, they didn't see me cry all the way home, how it takes awhile to get out of my car as I'm stiffened up, how I lay with ice, taking meds & using my hand held tenz unit. How I cancel suicidal activities because I can't move after a 5-7 hour day of non stop cuts & color, etc... I have a feeling most of you on here will understand where I'm coming from as people who don't have chronic pain have NO CLUE.
I'm hoping some of toy can let me know how this implants working for them most importantly. I'm also hoping some of toy can help me with the disability process.
Thank you for letting me put my story out here.
Blessings~ April
lindagkelly april_pain_1
Posted
My heart goes out to you. I worked for years with pain, but finally can't do it any more, but I worked until I was 60. I was 49 when I was hurt. I'm filing for social security disability. You should meet with a social security representative. Have you paid into the system? Yes, you can work and still get ssi. I can't remember how much, but I was kind of suprised at how much it was. I just googled it, and it said in 2014 the limit was $1090 a month. That's not bad. You need to file as soon as possible. And get an attorney. It takes a long time to get approved, and you can expect to get turned down and have to appeal. I think you might be a good candidate for the neurostimulator. I had a Medtronic that really helped with my legs. Hang in there. Please feel fee to talk here any time. We're all here for the same reason and we DO UNDERSTAND CHRONIC PAIN. And you're right, our families and friends just DONT GET IT.
God bless you,
Linda
lindagkelly april_pain_1
Posted
Did you say suicidal activities? Are you thinking about suicide? If so, please talk to us. Let us know. I know that it crosses everyone's mind once in a while, especially on a bad day, but if you are really thinking about it, please talk to us. Talk to someone at home.
I also noticed that you are a hair dresser. I have a suggestion, which you may already be doing. Don't reach or stretch to weird angles. Walk around so that you can do what you need to do without having to reach around at an awkward angle because that's harder on your body.
I know that you don't know any of us , but we do care.
How are you doing today?
Linda
kilee april_pain_1
Posted