Physical therapist recommendations?

Body: 

Recently in some thread or another Christine recommended the work of physical therapist (physiotherapist) Diane Lee in Canada (www.dianelee.ca). This looked brilliant to me --- someone who is actually using diagnostics to assess what muscles are doing, and to work toward better patterns of muscle use and balance, while being attentive to avoid further damaging lower back and pelvic prolapse issues. I'm about 2 months into a diagnosis of stage 2 rectocele, but my main symptoms, and the only ones I find so intolerable that I'm considering surgery if I can't find a way to reduce them, are very acute 1-2-day episodes of pelvic pain and/or lower back pain and instability. I injured my back last fall and think it likely that I never really returned to proper balance in using my abdominals/back musculature after a difficult childbirth 9 years ago, I just recruited whatever muscles were readily available and muddled along until increasing overweight and an overload incident pushed things to failure. I am doing the wholewoman beginning routine and attempting the posture, but I have always felt a bit daft in properly mimicking prescribed movements or orientations with my own body. I also feel that I may have more longterm muscle inadequacies or disconnects. I would love to try working with a physical therapist whom I could trust to be very diagnostic, to assess what's going on and perhaps find a program toward balanced muscular use which wouldn't strain all the wrong places, who could really give me feedback on what I can do that's constructive or destructive and try to reawaken muscles I fear are in disuse. At least I could learn if focusing on muscular development is an issue that could help my symptoms, or not . . .

Would anyone have any recommendations for such physical therapists in the Southeast United States (Atlanta, GA especially)? Is there a professional organization I could look to for a recommendation? What really appeals to me is the level of assessment and diagnostics Diane Lee's site describes, not just following a regimen but having some readout on what muscles are being mobilized, etc. Is there any jargon/label I should know for this approach, if I'm to google search for more local practitioners?

Thanks,
alphamom

Hi Alphamom

Robin has given you some good starting points. I think your idea of getting out of a *good* PT all you can is wise. As you have had the previous back problems there is no guarantee that the problems you are now having is directly related to your rectocele, thought he back problems may be aggravating the rectocele by not allowing the full range of movement, and the rectocele may be causing some back and pelvic pain, though nobody has ever found which causes what. They just seem to occur together.

You could end up having surgery and still having the pain, or else having another lot of pain as well. I'm not trying to be alarmist about this, but most conservative doctors will try physical and other non-invasive therapy first, then drugs, then surgery last of all, for almost any condition.

What impressed me with Robin's story is the whole body approach taken by her PT.

Hey, I just had another idea. What about contacting Robin's PT and asking her if she knows any other PT's in your part of The States who use the same model as she does? At worst she'll say no. At best you have some local leads to follow up.

Cheers

Louise

Well, I didn't get any word-of-mouth referrals, but I went through the www.apta.org website (I don't know if this is the only US physical therapists' professional association, or if there are alternative ones.) They have several specialist certifications and just established board testing for a women's health one this year. So, though I don't know too well the basis for their women's health certification, I looked for physical therapists certified in women's health and preferably orthopedics (for the lower back issues), then looked at whatever I could find of them online for their approach. I found one that has most of the techniques I was impressed with --- ultrasound imagery to detect which muscles were activating, the possibility to work on reinnervating muscles. Though she's out-of-network for my insurance, hence largely out-of-pocket, I have an initial appointment for next Friday!

I feel like I have learned what I can about the surgery, and as far as surgery goes, it's pretty gold standard, aiming for natural reattachment and avoiding egregious known dangers, by a very highly peer-regarded, publishing, academic surgeon. I think there's a very good prognosis that it would fix what my surgeon considers the obvious structural problem (and he's shown me through a rough pelvic exam that exacerbating the rectocele can cause an agonizing episode). But even a well-implemented and designed vaginal surgery is very traumatic. And the link between the symptoms I can't cope with - the acute pain and weakness episodes - and the simple presence of the rectocele seems tenuous to me. Better to at least exhaust every possibility to deal with the pain symptoms directly, first by trying to improve any muscle imbalances that contribute, with good guidance. I have never really managed to make progress on repairing obvious muscle deficiencies, not after childbirth when my lower vaginal tone was totally lost and remained unresponsive to kegels, and not after the more recent back injury. At worst I will learn something about my body, and better evaluate the unspoken assumption that this is as good as it can get without surgery. And I feel the handholding will make me more confident about implementing the posture, and maybe some of the elements like firebreathing and nauli that seem utterly baffling and a bit scary to me now.

I also feel I should give my recent switch back to hormonal birth control a chance to settle in. My cycle had been getting more acutely crampy, more frequent, more breakthrough in between, and seemed to be precipitating these episodes. It's as if I was spewing out progestins in an open invitation for any malcontent muscles nearby to cramp and spasm . . . and the ones that responded most strongly were the most susceptible ones due to old injury, overfull bowel/rectocele, etc. Regulating that cycle may get rid of some of the egregious triggers. My body's often been known to have reactions far worse than what triggered them --- fainting, asthma attacks, many ways to get caught in escalating feedback loops that are only cured by a full reboot. I think these pain episodes may be like that, some self-reinforcing cascade that becomes a much bigger problem than anything that started them. Trying to limit the hormonal triggers and at least knowing I have one tool to break the cycle (vicodin, though I've only used it twice) gives me a lot more confidence to patiently explore an approach like physical therapy.

Thanks,
alphamom

Hi Alphamom

Not sure where I read about it, but I have just started St John's Wort to try and lessen my muscle spasms that have plagued me on and off since a teenager. It is supposed to take a few weeks for clinical improvement. I have only been taking it for about a week but I do seems to be suffering less. It has also taken the edge off my irritability, which may be related to lessening of pain, but may also be its antidepressant qualities. It may also be because I have taken a positive step towards lessening the pain, so is a placebo effect. Who cares? I'll keep you posted.

Anyone else tried this herb?

Cheers

Louise