He went to see the Orthopedic surgeon yesterday.

He took 5 x-rays of Alan's foot. Then he made him stand in his bare feet and examined his stance, his arch, (everything about the lower extremities).

He told Alan, you need the bone shaved (under the foot ulcer), and you also need the muscle in your calf, extended. I see the way it's putting pressure on the bone underneath the foot". (I wasn't there, but Alan remembered everything the Ortho said).

So February 14 is the due date. He will be in a cast for 3 weeks (on crutches too), and then the shoe boot thing for another 3 weeks.

And the ortho is consulting with Dr. Fred. The ortho gave Alan a big folder thing with instructions on when to get the blood work. So Alan will follow procedure.

I guess it's all been pointing to this for a long time.

Alan is worried about one thing. Not the operation, he knows he'll be put out for that and he had no problem with the former foot surgery for his tailor bunions (he asked if this guy would do the other tailor bunion and the guy said "Is it giving you any problems?" and Alan said 'no" so the guy said 'we're not going there then".

But Alan is worried about the pain afterward because he'll be in a cast, and he has to shake his foot when he gets the PN pain. I told him 'they will give you something for the pain", He doesn't use any pain meds now, he just uses his massage thing on his legs and the pain goes away. Other than that, he just tolerates it.

But what happens after this kind of surgery is anyone's guess.

I would have asked the doctor how high the case will reach. I mean does it go right up to but below the knee (so he can flex the leg), or will it be a full leg cast??)

I wish he would have asked.

So he's having two things done, the shaving of the bone, and the extension of the calf muscle.

If anyone knows any info about these things, now's the time to start sharing.

lol

Melody

I know the surguries I'd had since I got PN took a longer recovery - Dahlek I'm sure will pipe in - but you need to talk to doc about best time to get IVIG in relation to surgery to help him recover best he can..... also, anesthesia seems to hit much harder with the PN - so I'd be sure to discuss with anestheisologist prior to surgery....

Well, hopefully Allan will be up and about by Spring. Let's hope this works for him. It has been a tough problem and I am sure he is sick of dealing with it. I am sure his surgeon will put his heart into it...great date for a surgery....Valentine's Day.

I'm glad someone found something positive about this surgery. I call it "Valentine's day gift to his foot". lol

and Kmeb, what do you mean Anaesthesia is harder with the PN?? What should he be looking for?. Alan has had foot surgery before and it was just fine.

And the odd thing was that they gave him pain meds for afterward, and he never needed to take a single med. His feet are completely numb (except for of course the PN pain between certain toes.

And about the ivig and the operation. We don't even know if he gets to get another IVIG treatment. they now demand a $500 co-pay with each treatment. That's not going to happen. Of course we are talking to people.

If he gets approved, (and the surgery is on the 14th of Feb), when's a good time to get the IVIG??

Mel

Mel,

I am sure the anesthesiologist will speak with Allen if they are doing anything more than a local. I don't know if he is getting a general anesthesia or regional or local. They tend to avoid general anesthesia as much as possible, so just ask.

Some people with PN have problems with some meds, but we are all different. Some people with PN, especially those with idiopathic small fiber, may have other diseases, some of which are associated with anesthesia complications. I am one of those lucky people who has general anesthesia problems....other folks breeze thru things. I am an anesthesia nightmare....but it might not be the PN....it might be what is causing the PN that also causes the anesthesia and drug problems for me in general. That said, PN is a disturbance in neurotransmitters and that is what an anesthetic does....so, yes it is always good to let the doc know....I bet you already have!

HI Mel and all!
I have problems with anesthesia too.....it doesn't work for me. They have to give me heavy doses of the stuff and Fentanyl based anesthesia doesn't work at all on me. I've wondered if it has to do with me PN or not.
I hope Alan breezes though this surgery and is up and running by spring!

are going on at once?
OK think, read and learn as as possible about the surgery Alan will be having. The prep parts are usually the easiest, as is surgery itself. RECOVERY afterwards is a bum deal all around tho! Recovery, not using that foot at all, losing muscle tone and able to do only very limited exercising makes one weaker than ever imagined. I speak from experiences having had to be off feet, tho not in casts, for the last 2 years running [plus a knee surgery a few years ago as well]. Time to ask questions about physical therapy is NOW! For my knee surgery I'd done 4 weeks of PT before the surgery and another 4 weeks more 3 weeks after. Now is the time to learn the key strength building exercises that can be done at home in prep and what to do during recovery.

SECOND relates to the anathesia? Alan has a 'demeyelinating' condition with his CIDP. MS is also a 'demeyelinating' condition and many anathesias can do more 'demeyelinating' due to the meds used. The MS communities are the ones who are best versed about this. If you even do a search here, using 'MS+Surgery' I bet you will get an eyeful and earful...There are other meds used that can help avoid more 'demeyelination'. As long as the docs and the anathesiologists KNOW about the connection with that key word: DEMEYELINATION...I have had 3 surgeries since my CIDP onset and speaking up and loud about the D-word I've not had problems..ounce of prevention or caution for sure. CIDP and MS are different in that the D-word occurs at opposite ends of the body...so to speak -MS in the brain, CIDP at the 'extremeties'.

THIRD AND LAST, the IVIG and timing: I have been told by my neuro that a wait of 7-14 days...ideally 10 days after an infusion gives you most benefit for the condition you are getting the IVIG for, and yet you still have enuf 'boost' from the IG to help keep infections at bay. As for the pain pills? After surgery they WILL be a must! I didn't need to take my full 10-day supply of Oxy...I believe I only took 5 days for the first surgery, 4 days the second and 2 days the last. Along with a LOT of peri-colace for the Oxy side effects! Keeping well hydrated during recovery and moving about a little bit [ergo the pt at home exercises] will help stimulate circulation overall and minimize side effects for the long run.

Sure hope this helps ease your mind and preps YOU for the whole experience! Alan is truly lucky to have you to care for him! I did 90% of my recoveries on my own...and I know how hard it is just to get a bottle of water from the kitchen to my 'chair', then other trips. You should/must make him move as much as possible tho...surpising how a person can adapt and do it when they have to..I believe that helps speed up recovery too! - j


Roxie It does have something to do with the PN....now you know.

HI J!
Yep I do know! I sure get some strange looks from nurses tho when I say I want to talk to the anesthesiologist myself! I don't take that look for an answer anymore! If I have to have any more surgeries at that hospital I'm going to ask for that anesthesiologist because he was great! I've had some real turkey's before!
I've learned to bump up my Lyrica when I'm having something medical done now......never do the "wait and see" anymore!