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Re: About PN forums, please remind everyone......

Posted: Tue Jan 01, 2013 7:25 am
by oldcarguy
I too have been looking for some stats showing some proof of success before considering the surgery, mainly because the surgery is a no going back decision. What I got from the doctor (in Houston) was a flat 1/3 get "cured", 1/3 get better, and 1/3 no improvement. Ok, well gee that's not really a whole lot to convince a person to take the plunge. Like has been said by Greg, the websites only seem to give the negative side of the outcomes but where are we supposed to get info to make us feel confident about the surgeries if the doctors don't really give you anything?

Re: About PN forums, please remind everyone......

Posted: Tue Jan 01, 2013 10:46 pm
by Violet M
I think people who are in serious pain don't have as much trouble making a decision about surgery as those who have more moderate symptoms. For me it wasn't so much whether to have surgery as it was who to go to....

Violet

Re: About PN forums, please remind everyone......

Posted: Wed Jan 02, 2013 9:41 am
by Dizzyblonde
Hmm Violet, I'm seeing your point more and more. I'm looking for facts and figures everywhere and hoping that I'm going to recover over time and am prepared to put the time in if necessary. At my level of disability sadly I haven't seen any evidence of that. But one thing is for sure, the very scanty statistics on success as mentioned by oldcarguy
oldcarguy wrote:What I got from the doctor (in Houston) was a flat 1/3 get "cured", 1/3 get better, and 1/3 no improvement. Ok, well gee that's not really a whole lot to convince a person to take the plunge. Like has been said by Greg, the websites only seem to give the negative side of the outcomes but where are we supposed to get info to make us feel confident about the surgeries if the doctors don't really give you anything?
I have recently heard the same stats elsewhere and also think that I might just take the plunge. I'd give anything for my life back, even slight improvement might be better than the grim alternative. Sorry to sound so negative, I'm a bit fed up with all of it! Support amongst one another on this forum is also very important and I couldn't get by at the moment without it.
Judy

Re: About PN forums, please remind everyone......

Posted: Wed Jan 02, 2013 10:45 pm
by Sallyg100
Thank you for posting this. I was feeling really hopeless until I read your post.

Re: About PN forums, please remind everyone......

Posted: Thu Jan 03, 2013 12:27 am
by Jax87
Thanks Greg for reminding everyone of this. When I first came to the website I was very despondent because it didn't look like that many people were getting dramatically better. However, over time I did see some people's improvement, including my own. Now, I pretty much just check the site from time to time to see what's going on.

I'm still waiting to get my hip surgery and going to orthopedic pt in the meantime. I no longer have trouble in my sit bones with sitting, only in my groin area due to the hip impingment. I'm able to have sex regularly for the first time in my life, even if it still is not 100% pain-free. I hope that after the hip surgery recovery I will be able to reduce my cymbalta and lyrica dosages and maybe be able to be more active. Like HM, my recovery has not been due to PN surgery, but I would never have figured out how to deal with it without the internet. I'm not a full on "success story" quite yet, but I think I'm getting pretty close.

So, I agree that there must be other people out there who have improved and do not post much anymore or never posted to begin with. Thank you all for your continued help and support.

Re: About PN forums, please remind everyone......

Posted: Sun Jan 27, 2013 1:19 am
by Quilter 2
Hi Greg and everyone;
Guilty with a capital G for not returning earlier to speak of my small / big successes.
Nov 1 2011, I had surgery on my right side. Wow just writing that makes me wonder where the time went. I'm 14 months out and I have had some great days and some not very good. The really bad times came from the fact we moved in June from VT to TN. The 1000 mile one way ride was not a great idea for someone only 6 months out of surgery. From May to July of 2012 we made 3 trips back and forth. 6000 miles. Once we finally settled into our new home, stayed out of the car, got unpacked and did all the other stuff that comes with moving, lights turned on, drivers lisences, registrations, setting up banks ect., I felt better. I try to walk as much as possible and that sometimes makes my leg ache and causes more burning. I have taken myself off of most of the meds. I take 300 mgs. of Tramadol a day. On a really good day only 200 mgs. About 3-4 times a month, I need the Valium suppository, and 250 mgs. of Gabapentin in the AM. I think that's pretty good but I haven't had a pro tell me that.
I need to think before I do some things. I picked up a shovel to move a little snow the other day, yes, it does snow in TN(not much) and my husband almost killed me. I heard for at least an hour how chopping ice put me where I am today. See, I was having a great day and just didn't think. He's right, but I hated to admit to it!!
For all of you not knowing whether or not to have the surgery: I had Dr. Conway, whom I like very much. I tried shots, PT, traveling to Phoenix for second opinions, different meds, traveling to NYC for Dr. Potters MRI. I wasn't getting any better so I figured what the hell?? As of a year ago, I didn't feel I had any other options or things to try. There was a time when I wished I didn't have the surgery. After the pity party, and realizing that life was going to be different, I was glad I had it. I'm better now than before. From what I've read, the turning point is 18 months. Dr. C told me I should know at the 2 yr. mark what the rest of my life will be like, (my words, not his)
One day I drove 220 miles with NO flare. Another day, I just puttered around the house and hurt like hell. Who knows? I am aiming to get back on the motor cycle. I may find out after the ride that I will never be able to do it again but I will try this summer around my 18 month mark.
I do apologise for not getting back to this wonderful site that saved my sanity. I guess, I just didn't want to ever see a computer or phone again. I don't even do much E-Mail wise. Just burned myself out with the researching.
My best to you all. No matter what you decide to do, there are always good days in one form or another. Some are just not painless. I don't believe I will ever be pain free, but I will always make the best of it with my family and friends.
Love to you all
Doreen

Re: About PN forums, please remind everyone......

Posted: Sun Jan 27, 2013 1:45 am
by Violet M
Hi Doreen -- it's so great to hear from you again, and especially great to hear that you are having some good days! You know, I wasn't really able to count on a good day until 18 months post-op and even after that things have continued to improve. So you have good reason to be optimistic.

Wow, you've gone through some major changes since we last heard from you. Glad you were able to get through the move and get set up in your new home. Now, please obey your husband ( :lol: :lol: :lol: :roll: ) and don't do anything crazy. Would love to hear how you are doing at the 18 month mark. ;)

Hugs,

Violet

Re: About PN forums, please remind everyone......

Posted: Mon Jan 28, 2013 5:31 pm
by helenlegs 11
Thanks for posting Doreen, good luck for the future. . . . Your husband sounds very like mine. . . .if he even saw me with a shovel!!! ;)
Take care
Helen