Patient Testimonial: Cluneal Neuralgia - The pain is still there, but so is the fight to stay positive

Published Nov 7, 2019 • Updated Dec 11, 2019 • By Louise Bollecker

After several false diagnoses, Peggy found out she was suffering from cluneal neuralgia, a condition that causes such intense pain that she can’t stay seated for more than a few moments. In this testimonial, she talks about her journey toward diagnosis and her daily efforts to live a normal life.

Patient Testimonial: Cluneal Neuralgia - The pain is still there, but so is the fight to stay positive

Hello and thank you for agreeing to talk about your condition. Can you tell us a little about yourself?

I’m a 46-year-old woman who’s always suffered from health problems: slipped disks, sciatic nerve, cervicobrachial neuralgia, tendinitis, endometriosis, Irritable Bowel Syndrome, I could go on and on. I have three grown-up and beautiful children with perfect health and I love to help others.

When did your first symptoms appear?

6 months after I had a hysterectomy at the end of November 2016, I was suffering from incontinence and a slight pain in my groin. I was told to see my surgeon to make sure there were no problems linked to my operation. She immediately asked to do a pelvic ultrasound which showed that I had a prolapsed bladder and perineum.

That set off a whole production. I had to go see a urologist who had me do a whole battery of tests: cystoscopy, cystography and half a dozen others that I don’t remember the names of, but it lasted a year, with an appointment every two months or so. I had to undergo an operation to “put my organs back in place”. I found out I had a bladder and rectal hernia. After a year of waiting, I finally saw the head surgeon who directly turned me down. She said she wasn’t about to operate on me and also said:

"There’s no reason to operate on you. Your bladder is perfectly fine and you can live very well with a prolapse, besides I don’t know how you did it, but your prolapse is getting better and even moved up a bit."

"That’s probably because I have been living flat on my back for the past 2 months", I said.

"Then you need to keep doing that", she replied.

"I’m in pain", I told her, "It hurts so bad I can’t even stand up."

"A prolapse doesn’t hurt." she said, "If you’re hurting that means there’s something else that is going on, maybe because you had a recent death in the family."

Did your symptoms have an effect on your love life, social life, or professional life?

It hurt more and more to stand up and last September, I broke down. I went to see my GP who decided to put me on sick leave for the time it would take to get a handle on my pain. I haven’t been able to work since. Most of the time, I‘m lying down and I can’t see any of my old colleagues. I only talk with my aunt who’s like a mother to me and since I can’t stay seated I can’t go out to a restaurant, or to a friend’s house, or travel. Talking on the telephone is well and good, but after a while, you run out of things to say, especially when you have no social life and since I can’t feel anything below my waist, my sex life is shot too. My husband’s a good man, he has stayed by my side, but this is no way to live, always lying down.

Did you see a lot of doctors before you were able to get a proper diagnosis? What did you believe was wrong with you?

I went to see a gynaecological surgeon who specialised in endometriosis, then I went to see a urology surgeon who told me, wrongly, that I had a prolapse and that was what was causing the pain, and then the head surgeon. I thought maybe I was hurting because of the bladder and rectal hernias: since they were tangled up with each other, that must have been what was pressing on my bladder…I went to see a gastric surgeon who told me there was nothing wrong there, that it was a neuropathic issue, without explaining to me what that meant.

I’ve seen my GP God only knows how many times. I went to the emergency room twice, but they told me to wait until I did an EMG (electromyography). I’ve also been to a general medicine specialist that told me that it was surely pudendal nerve neuralgia but we had to wait for the EMG to know for sure. And finally, I went to a pain specialist who was the only one who could tell me what was actually wrong with me.

When did you finally get the correct diagnosis? How did it happen and how did you feel?

I was diagnosed on the 28th of August, 2019, the doctor finally understood what was wrong and she told me, “It’s cluneal neuralgia”. It was almost a relief to hear the diagnosis; that this wasn’t all in my head and that what I was feeling was real... that it was this nerve that controls the lower abdominal and gluteal muscles. It was aggravated by the fact that my hip muscles had atrophied due to lack of use. When my organs fell down, they pressed on that nerve and caused my hip muscles to atrophy. Every time I eat or drink something, my organs, which are already in a fragile state, work very slowly since everything is knotted up from all of the surgical interventions and the delayed diagnosis…Everything got inflamed because no action was taken.

When I stand up, it presses on those muscles and the muscles don't can’t understand why they’re being called on to do so much work, causing them to contract as hard as they can... which is where the pain was coming from.

You were prescribed specialized osteopathic and abdominal-genital fasciatherapy sessions, how was that?

The osteopath was very kind, she took note of all the notes from the doctors I had seen. She asked me how I felt, where I hurt, and did a surface exam. She explained to me in detail what was wrong with me and what she was going to try to do to help me.

I laid down, and she tried massaging my swollen stomach. She asked me to breathe in and puff out my stomach. My stomach puffed out on the top but not on the bottom. She massaged it gently without hurting me, and then she pressed lightly on the nerve so that I could know exactly where it was. It was quite painful. She then asked me to sit down and she put her hands under my backside to see where the pain was coming from. As soon as I put my weight down on her hands, in just a few seconds, the pain was unbearable. She then observed me as I took a few steps.

She told me to wait 48 hours before I did anything of of large effort, and that I should rest for the time being.

Do you still get treatment for your condition?

I take 600 mg of Pregabalin (e.g. Lyrica), spread out over 4 times a day. Acetaminophen paired with Tramadol when I’m hurting and 3 to 5 drops of Amitriptyline. For my stomach, I take 2 Phloroglucinol tablets before every meal, a dose of Gaviscon and an Omeprazole (e.g. Prilosec OTC) tablet once a day. I also take one dose of Polyethylene Glycol 3350 (common brands: MiraLAX and GaviLax) a day for constipation.

Do you do any sort of athletic activities?

I have physical therapy twice a week, which includes stretching exercises and perineal therapy. Once a day I use a device to stimulate the nerves. I don’t use seat cushions. For the moment, I’m not due for any more surgery; we’re waiting to see how I respond to my current treatment.

How do you feel now? And how do you stay positive?

I stay positive because I must. I still have my third child to raise, so I can’t lie around like a vegetable. I’m in pain, but I still have to laugh sometimes... you just got to. My older children also need me, so I can’t quit just yet.

What are the symptoms that won’t go away? What’s hardest for you during the day?

The pain is still there despite all the medication I take, and even if it’s hard to stay standing, I feel like I’m getting stronger, and I’m able to walk longer distances.

The hardest thing is having to do everything standing up or lying down. I’d love to sit down, go to the cinema or even to a restaurant. It’s hard not to be able to do those things.

Do you feel like your friends and family support you?

Yes, anyone who’s close to me knows I don’t complain for no good reason, and they want me to get better. My husband would like to be able to do more for me, he feels useless sometimes and my children all want to see me get better. My youngest hates to see me like this; he’d love for me to get up and move about, so he gives me little pinches on the arm or the ears and other bothersome things. I’d like to be able to go outside with him, but I can’t, so I keep quiet.

I’m the secretary of a renter’s association. the president is a friend of mine who thinks it’s all a little in my head, and that if I just got up and kept busy, I could get back to work and do the things I used to do... like help her with the association.

What advice would you give to a patient who’s still waiting for a diagnosis or just got diagnosed?

Whatever you do, don’t stop moving and get some help from a counselor (or a therapist) because you need to talk to someone who isn’t going to judge you. You’ve got to laugh a little and if you can’t do something you love anymore, find a substitute. For example, I replaced the cinema with Netflix and I watch a load of series and I play internet games, sketch – all of that calms me down. And most of all, don’t give up and let yourself sink into a funk. If you get depressed, call someone who can cheer you up.

Thank you Peggy for sharing your experience.

What about you? How were you diagnosed with Cluneal Neuralgia or a similar nerve pain/nerve entrapment condition? What treatments have you experienced with and what has worked for you?


avatar Louise Bollecker

Author: Louise Bollecker, Community Manager France

Community Manager of Carenity in France, Louise is also editor-in-chief of the Health Magazine to provide articles, videos and testimonials that focus on patients' experiences and making their voices heard. With a... >> Learn more


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