From Nutcracker Syndrome to Loin Pain Hematuria Syndrome & Acupuncture

Nutcracker Syndrome:

I was diagnosed with Nutcracker Syndrome or Nutcracker Phenomenon by my nephrologist a month ago after a CT Angiogram showed signs of a compressed renal vein. He sent me up to The Cleveland Clinic to be evaluated by a renowned kidney and urological doctor. During my appointment, the first of three I had up in Cleveland, the specialist explained that Nutcracker Syndrome is a controversial diagnosis and that there is usually a bit of compression of the renal vein in most people who are thin because there is less mass to “pad” the area. It can definitely cause problems in some people, but because I am having zero symptoms on the left side, we don’t need to worry about it. No need for surgery or treatment; unless, in the future there are complications, then we can readdress the situation. That is great news.

 The Cleveland Clinic is ultra high-tech! They have GPS clip-on tags that you
wear so they can find you when they are ready for you to come back to the room. Crazy!


This, however, left me without an answer to my burning (pun!) question: what is causing my right-sided flank pain? We needed to investigate further. We reviewed the CT Angiogram. We reviewed the previous abdominal, pelvic, and spinal MRIs. Next, we had to check my “plumbing” to make sure everything was working properly. Urology Doc performed a cystoscopy with bilateral retrograde pyelogram. I had to be awake for the procedure and it was uncomfortable bordering on painful, but thankfully only took about 15 minutes. During a cystoscopy, the doctor inserts a microscope up the urethra and looks around the bladder to make sure there aren’t any abnormalities or swelling, etc., then he sticks the scope into each ureter (the tube that goes from your kidney to your bladder, one per side), and flushes contrast up the reverse way the urine usually flows (hence the word “retrograde”), while watching this flow via x-ray. When all was said and done, we had two answers and one more theory.

Loin Pain Hematuria Syndrome:

First, my bladder, ureters, and kidneys are all functioning properly with no swelling, stones, or other issues. There is nothing that physically should be causing me any pain.

Second; for years I had many urinary tract problems and sometimes would be diagnosed with UTIs or kidney infections, and other times my tests would come back negative though I was experiencing pain, burning when urinating, etc. This led a previous urologist to diagnose me with Interstitial Cystitis, a painful bladder disorder that results from a too-thin mucus lining in the bladder allowing acidic urine to irritate the bladder walls. It made sense at the time, and I was put on a drug called Elmiron to treat the symptoms. The medicine was very expensive and wasn’t keeping me from getting what I call “flares,” so I stopped taking it about a year ago. Urology Doc said, though, that I definitely do NOT have Interstitial Cystitis, because the walls of my bladder were perfectly peach in color, with the only red being the normal blood vessels that are in the walls. There was absolutely no irritation or discoloration. So…that leaves me back where I was before the diagnosis: I get a lot of Urinary Tract Infections (UTIs) and have a lot of bladder infections and kidney infections. The good thing, I don’t have Interstitial Cystitis (for which there is no cure). The bad, I have no idea why I get so many infections or flares, or why sometimes the tests come back negative though I am in a lot of pain.

Lastly, we are left with a probable diagnosis for my flank pain…(finally!)…a very rare disorder called Loin Pain Hematuria Syndrome.

Let me just say that again: I have a probable diagnosis! We finally found out what is wrong with my flank! Oh my gosh! Jumping for joy!!!

Pain Management Doctor Visit:

After the Cystoscopy, I went to a physiatrist (pain management doctor) that works with Urology Doc to discuss all of the treatments I have tried for my flank pain and to make sure we weren’t missing anything. For example, do I have a spine disorder that we missed? Have I tried every treatment option available? Is there a different set of pain meds that might manage the pain better? This appointment went well, I suppose. The pain doctor and I went over everything I have done for my flank pain, listed here:

  • Pain Meds (Opiates and Non-Opiates)
  • Muscle Relaxers
  • Trigger Point Injections
  • Epidural Spinal Injections
  • Nerve Blocks
  • Trial Spinal Cord Stimulator (Neurostimulator)
  • Psychiatric Treatment
  • Chiropractic Care
  • Massage Therapy
  • Reiki
  • Essential Oils
  • Heat
  • Ice
  • Lidoderm Patches
  • Tens Unit
  • Ultrasound Therapy
  • Physical Therapy
  • Back Bracing
  • Volteran Gel
  • OTC Topical Rubs and Creams

The pain doctor said he doesn’t see anything else that could be causing the pain and that we have tried everything under the sun except acupuncture. He is a big fan of acupuncture and recommended that I try it for pain control before opting for the only other solution I have been offered: renal autotransplantation, which I will discuss a bit later in this post. So, at this doctor’s recommendations, and at the encouragement of Urology Doc, I must seek acupuncture before we move forward or take any other steps.

Urology Doc also will be contacting my psychiatrist here in Columbus, making sure that I am on a good treatment plan and that my pain isn’t in my head (oh joy!). He must make sure the pain isn’t being caused by my depression, that my flank pain isn’t psychosomatic in nature. Let’s hope my psychiatrist is on my side on this one. I have run the gauntlet before, even been through the psych workup before the Spinal Cord Stimulator trial to make sure I was stable and these symptoms weren’t emotional. I do hope he relays that, but he has only been my doctor for a year, not the entire four I have had the flank pain. I will have to wait to see how their discussion goes. I can’t handle another doctor saying this pain is “all in my head” like so many doctors told me before I got my Ehlers-Danlos Syndrome diagnosis.

 Location of my right-sided flank pain (old photos):

What exactly is Loin Pain Hematuria Syndrome and what does all of this mean? What are my options?

Loin Pain Hematuria Syndrome (sometimes referred to as Loin-Pain Hematuria Syndrome, Loin Pain-Hematuria Syndrome, or LPHS) is a rare and not-very-understood disease. According to Wiki, it is “the combination of unilateral or bilateral flank pain and microscopic or macroscopic amounts of blood in the urine that is otherwise unexplained. LPHS is considered a diagnosis of exclusion. The syndrome presents with hematuria (blood in the urine) and flank (a region of the lower back beneath the ribs and above the ilium) pain. The condition is very rare and predominately affects females. Worldwide, only several hundred cases have been reported. 

“The cause of LPHS is currently not known. One theory proposes that it is caused by a thin glomerular basement membrane and red blood cell (RBC) renal tubular congestion that leads to swelling of the kidney and distension of the renal fascia resulting in pain. At this time no cure has been found for this disease. LPHS is a debilitating disease due to chronic pain and the inability to know how to control the glomerular aspect. The pain of LPHS can be worsened by acts as simple as riding in the car and undertaking daily activities. Many people with this disease are unable to maintain employment due to the debilitating pain. The treatment of LPHS varies considerably from centre to centre. As the condition is rare and poorly understood, a widely adopted standard of care is not existent.”

To summarize, LPHS is rare, not well understood, the cause is unknown, and the diagnosis is based on exclusion — meaning the doctors rule out every other possibility under the sun until they are left with only one possible diagnosis: Loin Pain Hematuria Syndrome. There isn’t a test they can do to give you a definitive “yes;” the docs must work like sleuths until this is the only answer remaining. For me, the combination of everything the doctors have looked for over the years, the many tests I have done, the giant list of unsuccessful treatments I have tried, and the specialist, Urology Doc, going over every other possible scenario (to no avail) and then checking out my organs and urinary system to rule out any other renal or urological cause, has left us with just one diagnosis: LPHS. I have the intractable, idiopathic flank pain and microscopic hematuria, and therefore, that is the probable diagnosis. With only a few hundred people reportedly diagnosed with this, I can add my name to yet another list of oddities! What is up with my body?! I get all the weird diseases!

So, what am I to do?

I am working with the best team of doctors I could ask for. As I mentioned in the last post about this, the Glickman Urological and Kidney Institute at The Cleveland Clinic was just ranked number one (#1) in the country (USA) for kidney and urological diseases. The Cleveland Clinic is also ranked the number four (#4) best hospital in the country overall. The doctors are world-renowned. I couldn’t wish to be at a better place or have better doctors to help me in this journey. I am beyond thankful. We are doing a step-process; I am trying acupuncture first and if it doesn’t work, I will be deciding whether or not I want to try the only other recommended treatment – the last resort when pain meds aren’t relieving the pain: a kidney autotransplantation.

Maybe acupuncture will help; I don’t know. I know I believe highly in Chinese and Alternative Medicine. I am doubtful, because nothing has worked thus-far, but I am willing to give it a chance. Considering my options, and that I am required to by Urology Doc, I don’t have any other choice. I am trying to do the “zen thing” and go into it without any expectations, good or bad. I have signed up for twice-weekly acupuncture for one month to see if I notice any help, anything better than the Norco and heating pad.

Renal Autotransplantation:

If the acupuncture doesn’t work, I will have to decide whether or not to move forward with the renal autotransplantation. Let me explain to you just what that is:

A kidney (renal) autotransplantation is where the doctor does a kidney transplant, but with my own kidney. They would make an incision (I have the choice of one long one down the middle, about a foot long, or one six inch incision on each side of my body, two total.), remove my right kidney, and sew it into the left side of my body by my left kidney. The “hole” where my right kidney was would be filled with the intestines and other organs, things would just “slide” in place over there, and I would have two fully-functioning kidneys on the left side of my body. The idea being, when you remove the [right] kidney from the body, the one with the pain, you sever all nerves attached to the kidney. When the kidney is replaced in the other side, it now has no nerves, so I shouldn’t feel any pain from the kidney. An example of how this works outside of these circumstances; a person who undergoes a complete kidney transplant with another person’s kidney, feels no pain in that kidney even if the kidney has stones or other issues. It is because there are no nerves attached to the donor kidney when it is implanted. In the same way, my reattached right kidney would have no nerves and it should “fix” the pain issues I am having.

The doctors at The Cleveland Clinic perform this type of surgery often, for various reasons, most of them not related to LPHS. But, when a patient presents with LPHS and they have tried every other treatment with no success, they perform renal autotransplantation in a lot of those cases. The success rate for the body to receive the kidney and accept it, and have the kidney return to a fully functioning kidney, is about 95%, according to Urology Doc. That is a very high success rate. More than likely, if I had this surgery, I still would have two working kidneys. The tricky part in deciding whether or not to try this surgery lies in the other statistics; there is only a 50% chance that the autotransplantation will relieve the pain completely. There is about a 70% chance it will relieve some of the pain. So, I could go through the surgery, and have very minimal pain relief, or no pain relief at all. There isn’t any way to tell beforehand how the surgery will affect me, if it will be successful in pain relief or not. The other thing to take into account, there has been some evidence shown in a couple of studies, that the nerves that are causing the pain could regenerate in the transplanted kidney and I could go back to having the same pain I have now, just in a different spot. This is not-well researched, though, and some doctors believe it is impossible, with others saying it is very likely. Urology Doc told me it is unlikely, but can’t be ruled out.

The doctor doesn’t think that my Ehlers-Danlos Syndrome will pose too many problems. He is aware of the need for extra anesthesia and we also talked about doing stitches and glue (if we do surgery) like when I had my gall bladder removed, that way we ensure proper closure and healing of the incision. He also doesn’t think that there would be any problems stitching the kidney in place, but he will be talking to a connective tissue specialist if we decide to go this route.

An autotransplantation surgery requires roughly a seven day stay in the hospital and one month of being totally out of commission at home, then slowly returning to normal daily function over five or so months. It is a long recovery, and most likely even longer for me because I heal very slowly. The surgery would be performed at The Cleveland Clinic by Urology Doc and his team of experts. If the pain returns, there won’t be anything else they can do, and it would just be a waiting game to see if the autotransplant was successful or not in terms of pain relief.

There are some very successful statistics in the most comprehensive journal article on “Renal Autotransplantation for the Loin Pain Hematuria Syndrome: Long Term Followup of 26 Cases,” published in the Journal of Urology in 1998. Urology Doc says that not much has changed in the way they do these surgeries over the years, and so the journal article is an accurate representation of what to expect.


 “Purpose: We review the long-term results of renal autotransplanation as a form of nephron sparing renal denervation for patients with the loin pain-hematuria syndrome.

“Materials and Methods: From 1985 to 1997, after exclusion of other urological, nephrological and psychiatric causes for severe intractable flank pain and recurrent hematuria, 22 patients with severe debility and heavy narcotic dependency underwent 26 renal autotransplantations for pain control [22 patients, 26 kidneys, because some had this done on both sides/both kidneys]. Postoperative pain relief, narcotic use, level of function in daily activities and status of the autograft were assessed.

“Results: Median and followup was 78.5 and 84.7 months (range 30 to 138), respectively. There were 2 technical failures. Pain recurred within 2 years after 6 procedures, of which 3 resulted in transplant nephrectomy and 3 were managed with a reduced analgesic requirement. Of the 16 patients with a minimum of 5 years followup 12 (75%) were pain-free after surgery with 3 additional patients pain-free after transplant nephrectomy. Overall, 18 of the 26 autotransplant procedures (69.2%) resulted in pain relief, in some cases beyond 10 years, with patients returning to normal daily activities.

“Conclusions: Renal Autotransplantation results in durable narcotic-free favorable results in the majority of meticulously screened loin pain-hematuria syndrome patients. Although some failures, which usually occur within 2 years after surgery, can be expected, autotransplantation is justified as a nephron sparing denervation therapy for select loin pain-hematuria syndrome patients [meaning it is a favorable kidney saving, nerve severing option].

“[Mostly] Full Article:

“The loin pain-hematuria syndrome is a rare clinical entity, first described by Little et al, comprising intractable flank and loin pain with microscopic gross hematuria. The etiology is still poorly understood, and the diagnosis is made by exclusion of urological and nephrological conditions. Recent therapeutic efforts have been concentrated primarily on pain management, ranging from percutaneous regional nerve blocks to surgical sympathectomy to open surgical procedures. The latter include renal capsulotomy, vascular pedicle denervation, ureterolysis, nephrectomy and renal autotransplantation. First described by Aber and Higgins in 1982, renal autotransplantation as a nephron sparing procedure has since been reported as having favorable outcomes in the loin pain-hematuria syndrome in small series by Sheil et al in 1985 and 1987, and Chin in 1992. Other reports on successful cases have appeared in the literature. An important reason for preferring autotransplantation to nerve nephrectomy for pain control is that 30% of patients have bilateral, usually metachronous involvement. Although referred to as providing long-lasting effective pain relief, followup of these renal autografts, except for 1 case, has been relatively short at less than 4 years. Concern that pain relief may only be transient following renal autotransplantation has been raised by some groups, with reports of recurrent graft pain within 3 to 4 years. To address the issues of durability of pain relief with autotransplantation and to define further its role in the loin pain-hematuria syndrome, we report the results of 26 renal autotransplantation in 22 patients with a median followup of 78.5 months (range 30 to 138). We also include an update on the 10 patients reported on in 1992, at which time 8 of 9 with minimum followup of 1 year were pain-free.

“From 1985 to 1997 inclusive 64 patients were evaluated as tertiary an in some cases quarternary referrals to 1 of us (J. L. C.) from other urologists and nephrologists with the possible diagnosis of the loin pain-hematuria syndrome. All patients had severe loin pain and 54 had persistent microhematuria including 20% with periodic gross hematuria. Clot colic or severe bleeding episodes did not correlate with the timing or severity of flank pain. Ten patients had no or insignificant microhematuria with intractable flank pain as the only complaint.

“Patients underwent the standard urological evaluation for hematuria and loin pain outlined previously elsewhere. The diagnosis of the loin pain-hematuria syndrome was made only after exclusion of all other urological and nephrological causes for the reported symptoms. A formal psychiatric evaluation was performed when surgical intervention was contemplated, and narcotic dependency and pain management problems were anticipated. In addition, 6 patients had sympathetic nerve blocks as part of the assessment. Of these patients 3 had transient pain relief and subsequently underwent autotransplantation. We did not perform this procedure routinely as a prerequisite criterion to surgery. Surgical candidacy was based on satisfying the 4 criteria of absence of urological and nephrological causes for the symptoms, formal psychiatric evaluation, excluding underlying major psychoses, significant narcotic dependency and significant debility from pain causing disruption of employment and daily activities.

“The majority of cases deemed unsuitable for autotransplantation were rejected because the degree of pain or disruption of daily activities was judged not severe enough to warrant surgery. Five patients had definite underlying conditions identified during the psychiatric assessment. The patients who did not satisfy all criteria were referred to a pain management specialist or psychiatrist for treatment, whichever was deemed more appropriate.

“Patients who presented with contralateral flank pain subsequent to the first autotransplantation were reassessed using the same standard investigations and criteria listed previously. The decision to proceed with a second autotransplantation was made independent of the outcome of the results on the first side, although the patients were advised of the increased risk because of the possibility of technical failure leading to dialysis dependency. The same strict criteria had to be satisfied before the second autotransplantation was performed.

“A total of 28 autotransplantations were performed in 15 women and 9 men 21 to 55 years old (median age 36.2) with the loin pain-hematuria syndrome. Two patients with followup of less than 30 months were excluded from the analysis, and 4 underwent sequential bilateral procedures. The standard living related type donor nephrectomy via a flank incision with complete division of the ureter was performed in all patients. An unusual finding encountered in a small number of patients at nephrectomy was an excessive amount of perivascular adventitial nervous and fibrous tissue. A standard Gibson renal transplant incision was used. The usual vascular anastomoses to the iliac vessels were performed (end-to-side anastomosis to the external iliac vein and artery, except for 4 cases of end-to-end anastomosis to the internal iliac artery). The ureter was reimplanted using an extravesical approach in 22 cases and transvesical approach in 4. Postoperative pain control was managed by the pain management team with patient-controlled analgesia using intravenous narcotics, switching to oral analgesia and tapering off the dosage as soon as possible. The psychiatrist and pain management team who had assessed the patients preoperatively were involved in the followup, providing the necessary support.

“Renal autograft function was assessed in the early postoperative period by a nuclear renogram in the first 12 cases, while the latter 14 were assessed with color Doppler ultrasound. Analgesic requirement was recorded before and after surgery, along with the level of daily living function. Updated data on the earlier reported patients were obtained by direct patient telephone interview or through local physicians. The procedure was judged successful by improvement in pain control leading to freedom from chronic narcotic usage, return to gainful employment, normal daily living activities and satisfactory autograft function.


“Followup of the 26 cases ranged from 30 to 138 months (median 78.5, mean 84.7). The current status of the autograft and pain control is listed in the table 1. Since patients who underwent bilateral procedures may have discordant results on the 2 sides, the denominator for the success rate was the number of individual autotransplant procedures rather than the number of patients. There was 1 immediate failure in patient 11 with renal vein thrombosis resulting in transient nephrectomy on the postoperative day 2. Left graft ischemia was demonstrated in patient 6 on postoperative Doppler ultrasound, and persistent pain necessitated transplant nephrectomy 2 months later. In 6 other cases pain recurred at the graft site, usually within 1 year. Of these 6 patients 3 have subsequently undergone  transplant nephrectomy and have remained pain-free. Three patients still have the graft in situ, 2 periodically need narcotics and 1 uses nonnarcotic analgesia. The remaining 18 of 26 autotransplantations (69.2%) can be classified as long-term successes, although 3 cases with recurrent pain, reduced analgesic requirements and less severe disruption of daily activities could be classified as partial successes.

“Patients 1, 2, 4 and 6 underwent sequential autotransplantations. Patients 2 and 6 had successful procedures on both sides, although success or failure on 1 side did not necessarily predict the outcome on the contralateral side. Three other patients had undergone prior nephrectomy on the contralateral side elsewhere for pain control and, thus, autotransplantation was performed on the solitary kidney. Histopathological examination of the nephrectomy specimens revealed the expected ischemic changes in patient 11 with postoperative renal vein thrombosis and patient 6 with graft ischemia on the left side. However, the remaining kidneys did not show any consistent histopathological condition. Of 5 kidneys 1 stained positive for the third component of complement.


“Since the etiology of the loin pain-hematuria syndrome is poorly understood, numerous medical and surgical treatment modalities have been tried with little success and, thus, most therapeutic efforts are now directed toward pain control. A sympathetic nerve block has been used by some as a preoperative procedure to differentiate visceral pain from nonorganic pain, although with our limited experience we had not found that essential in our management decision process. Attempts at renal denervation have met with transient success, although Andrews et al recently reported cures in approximately 25% of patients with chronic renal pain (not necessarily the loin pain-hematuria syndrome) via surgical sympathectomy. However, a significant proportion of the patients underwent multiple procedures.

“As a natural extension of the principle of renal denervation, renal autotransplantation has been used increasingly in serving renal function of the involved kidney. The initial reports were encouraging, and early results from our center revealed an approximately 90% success rate. These favorable figures were corroborated by Weisberg et al in their informal survey. However, concern regarding the transient nature of the pain relief derived from renal autotransplanation has been raised by some. As many as 75% of theses patients in these series have had recurrent pain and, thus, doubt has been cast on the long-term benefits of renal autotransplantation for the loin pain-hematuria syndrome. Renal reinervation has been suggested as the mechanism of recurrent pain in the autograft area. Canine studies have documented regeneration of autonomic nerves following renal autotransplantation. Similar findings have been observed clinically by Gazdar and Dammin, who described neuronal regeneration in human isografts and allografts. Since this reinervation process has been noted to extend to the interlobular arteries in some cases within 8 months of transplantation, recurrent pain in the autograft can be expected in a certain proportion of patients despite complete denervation at the time of surgery. The question of necessity to divide the ureter has been raised. We believe that leaving the ureter in tact would, at least theoretically, risk incomplete denervation or encourage reinervation of the autonomic nerves and, this, may jeopardize the success of the procedure. Therefore, our bias is that the division of the ureter may minimize the surgical failure rate.

“Since  the previous report of 1 failure in 10 patients, there has been 1 subsequent failure from that initial cohort. Patient 2 with failure on 1 side has subsequently undergone successful autotransplantation on the contralateral side with followup of 68 months for that autograft. On the contrary, patient 6 who had a successful outcome on 1 side subsequently had failure on the contralateral side, although graft ischemia demonstrated on Doppler ultrasound was likely the cause. Thus, having expanded the original series and extended the followup to more than 10 years in several cases, the current series supports the notion that renal autotransplantation when performed in meticulously selected individuals provides long-lasting pain relief in the majority, although the long-term success rate is closer to 70 than 90% as previously reported. If the mechanism of failure is due to renal reinervation via the iliac vessels, it does not affect all patients uniformly. Pain recurrence appears mostly within the first 2 years after autotransplantation.

“There has been considerable evidence that a significant underlying psychopathological condition exists in these patients as summarized by Kelly. There have been proposals to include psychiatric assessment in the treatment algorithm before surgery. All of our patients had undergone formal psychiatric assessment to rule out obvious psychoses. Despite meticulous patient selection with strict adherence to the defined surgical criteria, there was still a 30% failure rate. Attempts have been made to delineate predictive psychosocial factors for outcomes with autotransplantation. However, it would be difficult to use undiagnosed psychopathology as the explanation for discordant results on the 2 sides in some patients with bilateral autotransplantations. The discordant surgical results of the bilateral cases mend lend support to the theory of neuronal regeneration being the mechanism of failure.


 “The loin pain-hematuria syndrome is a complex clinical entity which clinicians have attempted to treat, rather simplistically, with renal autotransplantation. Failures tend to occur within the first 2 years. The mechanism(s) of failure may be equally complex, with psychosocial issues and sporadic renal reinervation being operational. However, in the absence of other viable alternatives, autotransplantation does provide sustained relief and return to normal daily activities in some cases beyond 10 years, in approximately 70% of carefully screened patients.”

Okay, now that you got through that long article, I will quickly summarize: There is a 70% chance that autotransplantation will relieve pain. If it doesn’t work, it could be due to psychiatric issues or the nerves regenerating on the kidney making it possible to feel the pain again.

There is another article comparing Renal Autotransplantation to Radical Renal Neurectomy and the conclusion is that autotransplantation is much more successful in relieving pain. Also, there were more cases of probable nerve regeneration when the neurectomy was done. A neurectomy is where they open you up and instead of taking out the kidney, which in doing so severs all of the nerves, the doctor just goes around the kidney and cuts all the nerves they can find while leaving the kidney in place. It is a much less invasive procedure, but the problem, said Urology Doc, is that there are many nerves which are too tiny to see and it would be impossible to cut them all without removing the kidney entirely. If they leave any nerves there will still be pain. So, both this article and Urology Doc agree that autotransplantation is much more effective than neurectomy.

I found a nice article by Dr. Marc F. Brazie, Division of Nephrology at University of Maryland Medical Center, Baltimore, that does an interview about LPHS, if you are interested.


For now, I am going to acupuncture and will see what the results are. If it relieves the pain enough, I won’t need to worry about this surgery. If, however, it does not relieve the pain, I am seriously considering the renal autotransplantation. Urology Doc and I have decided that I will revisit him after this course of acupuncture to reassess.

My first appointment with the acupuncturist at Urban Acupuncture Center was last week. We had a brief evaluation and discussed our goals. We are going to treat the pain in my flank and also, from a Chinese Medicine viewpoint, my liver has a lot of problems, so we will help that as well. The place I am going to has a very unique setting, apparently very common in China, but just picking up some steam here in the states. It is one large room, a community setting, with 12 recliners. All patients are together in the same room having their needles in and relaxing at the same time. They base their fees on a sliding scale, and you decide what you can pay, $15-$40 per visit (plus $10 for the initial consult). Their goal is to provide affordable acupuncture to the community. Those of you who live in Oregon – that is where this got started here in the U.S. There are about 100 of these open space clinics in the states, so you can always look up acupuncture in your area and see if you have one.

According the my acupuncturist, I should see results soon. She said usually people feel some relief after the first visit, although, for me, it just caused a major flank flare-up. I will keep you abreast of the progress in future posts. We have me set up for one month of visits, twice a week.

Alright, I am exhausted and sore from typing, so I will catch up with you all another day. Much love and peace to you. For those of you with flank pain, I recommend talking to your doctor about LPHS. Happy International Day of Acceptance for those of us with disabilities!



  1. Paul A. Bohnen, MD

    Keep going, one day at a time. There is so much in medicine we don't understand, especially when considering the complexities of EDS…and how it contributes to everything else that is going on. It may be that there is a spectrum of things all related to one process higher up in the organization of things. Unfortunately, you're the one who has to live it. But, you'll be teaching us all, too. Do your best!


  2. Derek Desranleau

    Hi I hope this isn't weird – But today I may have been diagnosed with LPHS and I am kind of freaking out… I was just prescribed blood thinner as a potential help so I am trying that tonight, but this is after a 2 year journey of trying to figure out what is causing pain in my right side flank area (back into my front)… Please keep me updated as to what's going on with you – it's not a fun potential diagnosis to receive but I feel better seeing someone post about this recently!


  3. Erin W

    There's a big group of us on Facebook with LPHS. If you contact carol who runs the website she will give you more information. Most of them are very against auto transplantation, one of my best LPHS friends had it done late last year and although the kidney ended up dying her pain is totally gone. Good luck, will be looking forward to following your journey. I am considering an AT too, although here in New Zealand its not common practice.


  4. missamberlee

    I have had right sided flank pain for almost right years now. I tried accupuncture about a year ago for the pain and kidney infections and it really only made the pain worse. After trying to unsuccessfully donate the kidney (my urinary excretion of calcium is too high, making me a potential stone-former) I got a nuclear medicine scan to check on the function of both kidneys. Painful kidney is doing 52% of the work so I decided to go with the autotransplant in spite of my fears about the huge midline incision. It turns out that they can do the surgery laparoscopically (at least the nephrectomy part) so ill just have a few smaller incisions and one larger one. (Or two larger ones, counting the transplant site) My surgery date is just around the corner (May 29th) and I've been told to expect a five to ten day stay in the hospital. I am so ready for this, all of my fears about my multiple renal arteries and complications from surgery are being replaced with daydreaming about being able to run, being able to let a friend hug me without being terrified of the possibility of the pain that will come if they pat my back, stuff like that. I'm glad I found your blog and your drawing of the happy kidneys made me smile, thank you.


  5. sara58

    I have had episodes of horrendous flank pain since I was a little kid. Had everything imaginable poked in orifices and crowds standing about expecting me to urinate myself as they took radiographs. I have chronic hematuria. All sorts of theories and surgeries proposed, but no real diagnosis shows up. The last time I went in cystoscopy, my ankle was in a cast for repair of torn ligaments and displaced tendon. The surgeon had asked me if I had any other orthopaedic problems. Well, let's see …in the previous few years, torn rotator cuff, bilateral labral tears of the hips, and two back surgeries. He then asked if I could bend my fingers back…. I am headed soon for a third back surgery….then there's all of those bleeding problems that even the hematologist never could diagnose. I am just now beginning to connect the dots. Thanks for your blog. 🙂


  6. Anonymous

    I am a very slim person and have had the same problems as you describe. You might consider having a look at any upright and lying down regular x-rays you've had (if you had some) and check the location of your Right kidney when you are upright vs. lying down. It took 4 years of Right flank pain to find out that my right kidney was dropping into my pelvis (nephroptosis) every time I went upright and this did not show up on CT's since I was lying down because the kidney returns to the normal position when lying down. My left kidney drops some as well but not as much as the right. My nephroptosis happened due to ligament laxicity (ligaments not holding my kidneys up) but I don't have EDS and the laxicity was caused by another reason. Being slim can add to the problem. It takes a lying down and upright IVP study to verify the severity of it but a nephropexy (tacking up the kidney to the normal position)takes care of the problem. I had the procedure done myself. If it is severe it could cause hematuria due to stretching of the arteries, veins or stretching or kinking of the renal duct. It can also cause urine to back up into the kidney. It can also cause recurrent UTI's. Regarding Left Nutcracker syndrome as a possible cause for your hematuria. I would ask for a angiogram or venogram for this. They checked mine by angiogram after seeing it by CT and I had this condition as well. Everyone with this condition does not have flank pain because the left renal vein alternatively drains through collateral veins such as your lumbar veins into your spinal veins (and ovarian veins if you haven't had a total hysterectomy). When the left renal vein drains into the ovarian veins it can cause Pelvic congestion syndrome which can be very painful and cause various female related problems which I also had. Pelvic congestion syndrome can be seen on CT's but is often missed by radiologist and physicians. There are a subset of physicians and interventional radiologist that now believe that this collateral venous drainage which causes venous congestion also causes problems even within the spinal cord and can cause headaches and a bunch of other problems. Do a search on the internet for Nutcracker Phenomenon and you should immediately find a 2006 detailed medical article about this. I had to purchase the full 10 page medical article but it was well worth it. Also be aware that many people with Nutcracker Syndrome/Phenomenon also have Superior Mesenteric Artery Syndrome which is compression of the first part of the small intestine and this can can painful gastrointestinal symptoms. I have this as well. I hope this information helps you out. Take care, Dee


  7. Victoria Gail

    Hey there thank you for posting this I am almost in shock how similar my story is to yours. I'm a 20 year old female diagnosed with Elhers Danlos and loin plain Hematuria syndrome. I have intractable right flank pain with hemturia nausea and vomiting and having to go to the ER almost weekly to try and get help because I'm passing out from the pain and losing too much fluid. My nephrologist has no idea how to help. I tried a renal denervation which was unsuccessful and I'm stuck taking opioids for the past few years to try and help my pain which barely helps. I'm getting to the point where I'm ready to give up because I feel so stuck and so sick of doctors treating me like I'm making this all up. I would be so forever grateful if you see this if you could give me any advice or just let me know you read this. I don't know how to contact you other than the comments I'm so sorry I'll keep checking here! Thank you soooo much for writing this you are an angel I hope all is well for you!


  8. Anonymous

    Dear Victoria, Sometimes people with Elhers Danlos do develop nephroptosis due to abdominal ligament laxity. It can also cause hematuria. Right side nephroptosis is usually worse than left especially regarding symptoms and yes it can be extremely painful. So it sounds like it could be something to consider in your case. My right kidney dropped so much that it was lying on it's back in my pelvis. Looked like a bean on it's back. Lying down radiology studies like x-rays, CT's MRI's etc will not show ptosis of organs. I finally found this on some upright/standing vs lying down x-rays and then requested an upright and lying down IVP study to confirm the nephroptosis when standing. It was also putting tremendous pressure on my right Colon and causing downward placement of it into my pelvis and gas to even get trapped there. Sometimes this pressure on the Colon can even cause appendicitis or symptoms like appendicitis. I was in so much pain in my right abdomen, right pelvis, and right flank that my right leg would collapse from under me when I would try to walk. When I would go upright I could even feel the upper part of my kidney (a hardened area) in my right lower abdomen. Area next to and just below belly button. Stupid doctors thought for years I was constipated and it was my kidney they were feeling. Unfortunately people with EDS can also have gastroptosis and that is where the stomach drops into the pelvis as well. I have that also. This can cause nausea, vomiting and gas pressure, delayed gastric emptying, etc. Viseroptosis can be another problem in EDS and that is where the intestines drop into the pelvis which I also have. Go to this EDS web site and you will find an article that includes some of this information that you can provide your doctors. Go down to paragraph 5.8. Are you real slim, low weight? If you are, other things that can go along with the above are Left Renal vein entrapment and/or superior messenteric artery syndrome. Left renal vein entrapment can also cause hematuria. SMAS can also cause nausea, vomiting and sometimes excess gas in the stomach. In SMAS and gastroptosis, if a person can belch they might not have the gas pressure pain in the abdomen especially in the upper abdomen. Please keep me apprised of your situation if you would like. I'll try to check back often if not daily.


  9. kmb1072

    I have many doctors none of whom know what to do with me so they passed me back and forth each one doing nothing. I have severe pain and microscopic and gross hematuria. Is there anyone Who can tell me someone I can contact for more info. I am in the United States thank you


  10. JessicaLPN

    I was diagnosed with nutcracker syndrome and pelvic congestion syndrome, but experience no pain on the left side at all. All my pain is either right pelvic pain or right flank pain. I recently saw an interventional radiologist at the Cleveland Clinic who is the one who diagnosed me, but am now planning on seeing another doctor at University Hospitals for a second opinion. May I ask who you are seeing in at the Cleveland Clinic in case I decide to go back there? It would be extremely helpful. I'm on my 10th doctor and I'm sure as you know it's a frustrating process.


  11. Ashley Benda

    I was diagnosed with LPHS and I am having an auto-transplant next Friday, June 24, 2016. This pain is so out of control and i'm so sick of it running my life. I'm attempting to get it back through this surgery. I don't know what else to do.


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