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#1 of 11 Old 12-31-2011, 07:00 AM - Thread Starter
 
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Hi! I have read quite a few of the threads re: ETC. We just went down to see them on the 29th of January because of our 10 1/2 yo dd's bedwetting issue. Like many others, she also has not had a dry night since she was born. Very frustrating for her. I was also a bedwetter. So, this was nothing new to me. I had a "surgery" to correct issues with UTI that also "cured" the bedwetting. We have tried a number of things, including homeopathic remedies. Based on descriptions of people who have deep sleep disorders and observing my dd daily, I am pretty confident that this is the issue. However, like most others, the cost seems pretty prohibitive. To top it off, our insurance company has indicated they would be willing to consider a pre authorization, but need specifics of what they will be doing. They e-mailed us a letter to the insurance company that basically covers what is on their web page. That certainly won't convince the insurance that this is worth paying for. I understand that they tailor to each child and situation. Also, their "money back guarantee" doesn't apply to everyone. Apparently, because there is a history of seizures in our family, even thought my dd doesn't have seizures, this precludes us from that guarantee. Very frustrating as we know we need to do something for our dd...but don't know where to turn. Also, they talk about breaking the sleep patterns....that are genetic/inherited....how, by simply using an alarm, is this supposed to occur? I don't really get it and they seem reluctant to truly explain it.

 

Any help would be greatly appreciated. I not only want to help my dd with her bedwetting, but also with her sleep issue.

 

Thanks!

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#2 of 11 Old 12-31-2011, 07:04 AM - Thread Starter
 
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another question....do they just have the kids do kegels? What is strengthening the bladder? My dd had a leak issue a few years ago and we worked with a PT to strengthen the pelvic floor muscles. Worked well, but my dd is saying she is starting to have some leak issues again.

 

Thanks!

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#3 of 11 Old 12-31-2011, 11:04 AM
 
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I can't answer your questions, but I've read lots about food allergies and sensitivities and have read that bedwetting can be closely associated w/wheat intolerance. I too was a bedwetter, but "grew" out of it at a young age, and my best friend's daughter was as well. She didn't "grow" out of it til puberty started. Both she and I have celiac disease, but didn't find out til after the bedwetting years. It might be something to look at for you guys... It's a lot cheaper than going to a center, and seizures are on the list too (of things affected by wheat intolerance). So, many things could be related and corrected by something as simple as a diet change. I'm happy to offer support/recipes, whatever if you choose to explore that option.


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#4 of 11 Old 01-02-2012, 03:03 PM
 
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We are a private clinic that has been putting an end to bedwetting for 37 years and are able to offer a money-back guarantee.   Because we receive telephone calls from all over the world we understand how frustrated parents become when they have not been able to find a solution to help their child.

 

Prior to entering treatment we require a consultation with one of our directors, either by telephone or at our clinic.   At every consultation the following information is vital:   

 

-  Family history

-  Medical issues and medications used

-  Methods previously tried to end the bedwetting

-  All symptoms related to the inherited deep sleep and bedwetting

 

In response to the mom who recently had a consultation in our clinic for her 10.5 daughter who continues to wet the bed, we are offering clarification.

 

During her consultation the director was informed of a long family history of seizures and mom stated she currently is investigating her daughter’s possible seizure activity. While the bedwetting is not the result of a medical problem, an underlying medical disorder could adversely affect our ability to successfully end the bedwetting.  Mom was informed that if her daughter is diagnosed with an underlying neurological problems, the guarantee would not apply.  

 

Medical insurances routinely do not pay for non-medical problems.  As requested, we routinely supply information for flexible spending and health savings reimbursement.  

 

No two cases are the same, therefore, details are provided throughout the course of treatment by a trained skilled professional.  As part of our bedwetting treatment protocol, a biofeedback monitor is provided to gather necessary data.  It is simply a diagnostic tool.  We understand alarms alone will not end bedwetting.   

 

We always encourage parents to contact us directly should additional questions arise.

 

Warm regards,

Barbara Moore

Clinical Director

The Enuresis Treatment Center

www.NoBedwetting.com  

248-785-1199

 

 

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#5 of 11 Old 01-10-2012, 12:45 PM
 
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One of my ds wet the bed, what worked for us, in one week, was the potty pager that Dr Sears recommends. It is not an alarm in that it doesn't make a noise, it vibrates. Does your dd sleep through the wet? If so this maybe a good low intervention thing to try.

 

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#6 of 11 Old 03-03-2012, 02:18 PM - Thread Starter
 
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Just a follow up on my original post. After much research and testing for my daughter (to see why she was falling asleep during school work, hitting her head and not knowing why), it was determined that she did NOT have seizures, nor did she have complex migraines, and all of her blood work came back normal. So, our neurologist wanted to do a sleep study. The sleep study indiated that she did NOT have a deep sleep disorder either. On doing a lot of study on my own, talking to other clinics who were much more forthcoming and willing to work with our insurance company should that be the way we decided to go, we chose to go it alone. I bought overlays, a good mattress pad and an alarm. We worked with some of the basics found in a few different books written on the subject. We initially eliminated the pull ups, measured her bladder capacity and began "elevator exercises" as recommended by her pediatrician and a physical therapist who specializes in bladder and bowel issues. We also took her to our pediatrician to check and see if she had any constipation...which she did have a little and are currently working on eliminating so that constipation is not a factor. We also increased the fluids during the day to determine just how much she was drinking. Twice a week, we are also having her "hold it" for 5 minutes. And, she is practicing starting/stopping exercises to help strengthen the pelvic floor muscles. We intended on setting an alarm to see how easily she would wake up at night. Ultimately, a number of different things to see if she was ready for some type of program (we are basically using the waking up dry book, but have also read through 7 steps to a dry night as well as a few others which we borrowed from the library). Fortunately for us, we never had to use the alarm. Her first night without the pull ups, she woke up while emptying her bladder...she was able to hold it, get out of bed and go finish on the toilet. Since then she has experienced many ups and some downs. She has had 5 consecutive nights 100% dry followed by a night with only a little wet (finishing on the toilet). I understand that each child/teen/adult is different. I have a nephew that does not wake to his own alarm clock and still has sleep wetting. However, as much as a deep sleep disorder may be common in children who sleep wet, it isn't the ONLY reason. One of the books I read on the subject says that children wet in their sleep in ALL stages of sleep. There was a lot of other information that I read as well that was very interesting. I am SO glad that I did. By using all the information gathered, we were able to set up a program for our daughter that is working for her WITHOUT spending nearly $3000 on a clinic. In addition, our pediatrician STRONGLY recommended that we NOT use the alarm (I sent it back, we have never used it or needed it...I know this isn't everyone's situation, but it is ours). Why not use the alarm? Because their have been more recent studies that she has reviewed indicating that the alarm is MORE detrimental to the fatigue of the child (as well as the family). She personally recommended it for many years in her practice, but did not have patients with success. She has also had a number of patients who have gone to the center. Of those, she could only think of a couple of them that had success. We also have close friends of the family who went their and did not have success. I am not trying to put down the work that the center does. Having met the people there and read over the materials, I know they are genuinely concerned about helping people who have this issue and they are going about it in the way they believe, through their years of experience, to be the best. Kudos to them and the work they are doing trying to help people, like my daughter, to get over this. However, from my experiences, I would highly recommend that anyone who is dealing with this issue research, research, research. As mothers, and many of us attachment parenting families, we know our children best. Do what works best for you. If that is developing a plan/program of your own, like we did in our family, then go for it. If that is utilizing the knowledge of the different clinics out there, then do that. If you wonder if your child truly does have a deep sleep disorder, contact your insurance company and see if there are any reasons they will pay for a sleep study. My pediatrician told me that most insurance companies will pay for the study for possible diagnoses of apnea, fatigue and enuresis. I truly expected the results of my daughters study to come back with a deep sleep disorder. But, armed with the knowledge that that was NOT what was happening made it that much easier to jump into the program that we planned. As I have talked to her about her sleep and how rested she has been feeling since we started our plan, she has told me that she feels like she is sleeping better and is waking up more rested. I am thankful. I am hopeful, that by the time she goes to camp this summer, that she will be 100% dry. I was led to believe, by the clinic, that her case was complicated and that the likelihood of her being 100% dry in 9 months wasn't very favorable. After this first 3 weeks (of which she has had a total of 7-10 dry days 5 being in a row), I am confident that she will be dry before June. We know our children best. Do your research, and then do what is best for your child. In case you are wondering, I purchased my overlays, mattress pad (which has never gotten wet!), and the Malem alarm from the bedwetting store. You can be led to believe that you can't do this on your own. I have found, in our case, that we certainly can!

 

Thank you to those who also metioned the possibilities of allergies and/or celiacs. For many years, my daughter was allergic to milk, wheat and soy. According to our most recent visit to the allergist, she has outgrown them...and even when we were totally avoiding all milk, wheat and soy, she continued to have the sleep wetting. However, since we do have seizures that run in our family, I continue to keep that information filed away should I need it another day.

 

God bless you all on this journey as well as all others!

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#7 of 11 Old 03-05-2012, 04:41 PM
 
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Thanks for coming back for a follow up post!


mom to a 7 year old lego fanatic and a 5 year old cross dresser
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#8 of 11 Old 03-09-2012, 07:58 PM
 
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There was an article in a medical journal about a month ago that found that 80-something% of enuresis issues could be cured by addressing constipation.  Many of the parents had no idea that their kids were even constipated.  I know this was an issue with my son that we had no idea of for years--until it got so bad, that it became encopresis.  Cleaning out the colon, and then putting the kids on enough Miralax so that the stool was mashed-potato/ice cream shake consistancy was the cure.... and it took about 3 months.

 

Here's an article about the study...something to consider... :)

http://children.webmd.com/news/20120130/study-constipation-may-cause-bedwetting

 

 


Mom to DS(8), DS(6), DD(4), and DS(1).  "Kids do as well as they can."

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#9 of 11 Old 12-10-2012, 07:55 AM
 
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This is very helpful and interesting information. I would love to correspond about this privately as i also have a 10 yo dd who wets and a 7 yo ds with the same problem. I have similar books and have been hesitant to go it alone since it seems so overwhelming. You make it sound possible! Thank you!!

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#10 of 11 Old 05-12-2013, 05:18 AM
 
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I have a 7 year old boy that has never had a dry night. We have tried the alarm but we didn't have any success. I was considering the Enuresis Treatment Center, but now I'm having second thoughts. I don't mind putting in the work, getting up a million times at night or any of that, I just need an idea of where to start. Any advice would be wonderful!
 

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#11 of 11 Old 05-27-2013, 08:50 PM
 
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What she said.

 

Some good resources along those lines:

Cinncinnati Colorectal center website

It's No Accident by S. Hodges

yahoo group encopresis kids

 

Good luck!!!!!

 

Quote:
Originally Posted by umsami View Post

80-something% of enuresis issues could be cured by addressing constipation.  Many of the parents had no idea that their kids were even constipated.  I know this was an issue with my son that we had no idea of for years--until it got so bad, that it became encopresis.  Cleaning out the colon, and then putting the kids on enough Miralax so that the stool was mashed-potato/ice cream shake consistancy was the cure.... and it took about 3 months.


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