Originally Posted by DebDog (Post 659494)

I agree that the SCS is a lifesaver. I have my second one now. It helps my legs and I couldn't walk without it.


DebDog

Originally Posted by msdilbert2 (Post 670305)

DebDog: just read article on scs and it stated they work best for one leg. Sounds like you get pain relief for both legs (and lower back?) thanks, Pam

Originally Posted by davidhm (Post 685748)

I have been suffering from chronic pain for several years and now am at the point where the amount of oxy I require to control the pain is interfering with my life. This situation can only get worse as I get older and my body tolerates more and more stuff. I am also "labeled" as one of "those" who takes oxy for "pain". Even Walgreen's, in my opinion, discourages us "pain addicts" from filling their script in their stores. (I am retired and live in S. Florida where you can find a pain clinic as easily as a pizza parlour.)
So for all of these reasons I chose to explore a SCS and discovered this forum via a Google search. I am greatful for all the information provided. However IMHO the majority of posts are negative and spell out in detail the problems people have had with the SCS, their "reps" what ever they or their role is/are, their surgeons and their devices. At least I now have a list of issues to discuss with my pain person.
But I am left with a deep sense of unease. I can't tell if people who have had SCS implementation would have it again, would recommend to a family member or what the major trade off's are. It's like a virtual group therapy session, where everyone is right and everyone gets a group hug. You can't tell what real and what's not, what's fact and what a wish.
Maybe a disclaimer is in order. Maybe some real data from "poster's" is in order like age, length of time in "pain", kind of insurance, manufacturer, type of pain and location, etc.
The decision is get an SCS is too important and IMHO not helped by "virtual hugs". I don't write this to offend anyone, I'm only looking for a way to make this valuable resource even more so.

Originally Posted by Mark56 (Post 685934)

Hello David-

Sorry you haven't apparently knocked into the SCS/Pain Pump Subforum. We have a good many people who have worked through procedures there, both positive and negative. The majority of those among whom I have read of late have been of the more positive bent. A Thread chronicling my adventure through the process of having Boston Scientific Mini Rechargeable SCS is found there. Perhaps you did not give it a gander.

Now as to my age, since you ask, 56, hence my moniker Mark56. Would I recommend the process for consideration by others, not only would I, but I have given information directly to others who have asked. Would I have a family member go through this? Sure. My family can more truly speak to this, but, dear Visitor, you would need to read my thread to pick up on their perspective.

Stick around. We are pretty informative, congenial, raucous [well..... some are], and yearning to help others to try to have information to make better informed decisions for their lives..... yours included, my friend.

Hope to see you around,
Mark56:winky:

Originally Posted by davidhm (Post 685748)

I have been suffering from chronic pain for several years and now am at the point where the amount of oxy I require to control the pain is interfering with my life. This situation can only get worse as I get older and my body tolerates more and more stuff. I am also "labeled" as one of "those" who takes oxy for "pain". Even Walgreen's, in my opinion, discourages us "pain addicts" from filling their script in their stores. (I am retired and live in S. Florida where you can find a pain clinic as easily as a pizza parlour.)
So for all of these reasons I chose to explore a SCS and discovered this forum via a Google search. I am greatful for all the information provided. However IMHO the majority of posts are negative and spell out in detail the problems people have had with the SCS, their "reps" what ever they or their role is/are, their surgeons and their devices. At least I now have a list of issues to discuss with my pain person.

But I am left with a deep sense of unease. I can't tell if people who have had SCS implementation would have it again, would recommend to a family member or what the major trade off's are. It's like a virtual group therapy session, where everyone is right and everyone gets a group hug. You can't tell what real and what's not, what's fact and what a wish.
Maybe a disclaimer is in order. Maybe some real data from "poster's" is in order like age, length of time in "pain", kind of insurance, manufacturer, type of pain and location, etc.
The decision is get an SCS is too important and IMHO not helped by "virtual hugs". I don't write this to offend anyone, I'm only looking for a way to make this valuable resource even more so.