Thank you for this video. I've taken notes of everything you said, This past year has near enough ruined my life. I've felt that I don't want live. Like you I'm not suicidal at all I am so blessed with life but to live like this reaches hopeless moments. I'm constantly taken into A&E (ER) they've had to sedate me because I've been screaming so much for hours on end. My relationship has suffered greatly due to it. I'm about to have a Cystoscopy and Biopsy to properly diagnose which is scary in itself as I hear such horror stories about these diagnosis surgeries and I don't even know what will follow them. I've had many periods where I've slept in the bathroom with a blanket as I'm in such agony. I'm in pain 24 hours a day, I haven't slept for 12 months. I wake up every 20 minutes or so to wee. When I go to the toilet the pain is worse than being in labour with my son. It's like being ripped and stabbed with glass. I've known a lot of pain and experiences in my life but this is the worst. I'm trying to be as positive as possible and say what I'm grateful for every night. But it's effected every once of my relationships, my family, my boyfriend and awfully how I am able to take care of my son. Now I'm being seriously judged as I was housebound for 11 months. I've recently started going out of the house but only very locally, I can't get on a bus or be in a car for long. I take an horrible amount of prescription painkillers day and night including Valium, Tramadol and Codine. I hate that my 5 year old who I raise alone has to see me in such severe pain every day. I'm so desperate you guys. I refuse to give in to this. I will get better but oh my god it's awful. It's so awful. Sorry if this post has upset anyone, I rarely talk about this. It's a nightmare. I won't give up. I send love to all of you, we WILL get through this and be rewarded by the universe in beautiful ways. Love to all LollyBon xox #England
dear lady my heart goes out to you i hope your situation has got better? i dont suffer nothing like you but i get terrible sickness and am stuck on a chair with a bowl underneath just peeing it happens every few weeks i dont know whats causing it im menapauseal dry other bits dont help/ my realationship has sufferd badly cant do much but feel sick and awfull/im chaanging my diet cutting out alot of what i think is causing this its the not knowing and people who just dont understand how truely horrid you feel for days on end sorry about spellings god bless you and your son many women are suffering from all this painfull branches of this tree xx
How hard is this .! I’m going insane . 16 years for me .l also get up every 20 min at night . My mental Heath is just hanging on . Nobody understands and to read your story blew my mind because everything you say is me 😔.. lm a single mum also ,my son is 25 now . I’ve taken all sorts of stuff to get sleep but the pain wakes me up every time! Most days l feel like lm loosing my mind .l soldier on somehow.
After living with IC for more than 30 years, I was delighted to find thes videos. I am currently in a major flare up after ankle-replacement surgery and getting rescue treatments. Thank you for all you do, Jill. You know that your help is life-giving and hope to many of us!
Thank you so much for all you do. Thanks to the Internet so much suffering can be avoided. I almost feel blessed in the misery - cause very rapidly I was able to understand what it might be and take actions at once. 20 years ago I wouldn't even have known that I should stop coffee so I'm grateful I can learn on sb else's experience even though I'm devastated that so many people are in so much pain. I don't have pain but I'm so afraid of it. Thank you again and be well . I will watch and read all there is and when I'm healed, I believe I will, I will do my best to help others as well.
The very fact you cite Cyclosporine is an indication of an IC/autoimmune connection, something I discovered in the course of doing a lot of research on the Net. In my case, I had stopped taking another immunosuppressive med, Imuran, which I've used for Crohn's Disease and shortly after stopping my intake, I got the IC. Of course, IC wasn't the first thing considered; I've also had UTI's likely due to an enlarged prostate but a urinalysis along with a CT scan and finally cystoscopy suggested to my urologist that IC was the most likely culprit(esp. because of chronic pain and excess urination). So Imuran CAN work but it isn't as fast acting as I imagine Cyclosporine to be, usually requiring a 2-3 month time period to take effect.
I just saw a commercial on TV for Cancer Centers of America. A woman with bladder cancer had her bladder removed and the surgeon took part of her intestine and created a new bladder for her and she is now doing fine. Got me thinking. I have had IC for about 15 years and reacted to Elmiron, have had bladder instillations of DMSO with severe post pain. altered my diet, tried to manage stress, which always causes a flare.My urethra is severly damjaged due to many cathiters through the years. Currently trying Aloe Vera. Now I have been on narcotic pain medications every day to manage, and that seems to be the only thing that makes the quality of my life like other normal people. I wish they could just find a cure!!!!!!
Good, but you didn't cover pain management. Also you didn't warn patients that bladder instillation can cause damage to the urethra and make pain even worse. You also didn't cover that many people who suffer from chronic pain typically have extremely low levels of vitamin D. The reason many people don't go to level 4 or 5 is because they are not solutions to the problem and cause further problems. Also cover the long term effects IC causes such as lack of sleep which in turn can cause heart problems, weight gain, etc etc.
The video was already 25 minutes long. Further, it seemed to me the doctor was very good about wanting people to try less invasive, less risky treatments first. I don't think it's fair to demand that a person act like a robotic encyclopedia when she's obviously thought through a massive quantity of data and presented a solid, comprehensible narrative.
Thank God I found your channel! First I want to thank you for everything! From the botyom of my heart! I have Severe case of IC for 5yrs. Hunners ulcers, bladder spasm, OAB, in diappers 24/7 because - voiding more than 100x day :( Also have IBS with big impact on my bladder, almost like nerves are so connected that pain travels... Trying to do Candida diet myself but its hard because with all my health issues there are just a few things I can eat and feel I have nutrient deficiency. Taking Aloe Desert Harvest for 3yrs now....should I stop for a while or is it safe to take it for years? I was takinh Hydroxizine Hcl for 3yrs thought it helped, but than decided to stop, (dry eyes I could bearly have it open)and also have arrhythmias so dr said its nit good for prolonged usage especially for heart.... Thank you so much for everything, you gave me BIG HOPE!!! ❤️❤️❤️❤️🙏🏻🙏🏻🙏🏻🙏🏻 I wish you all to find the cure, lots of love!
Hello Jill. Excellent video. I have been taking Hiprex for almost two years for reoccurring UTIs which I've had all my adult life. Hiprex makes the urine acidic so bacteria can't live there. But could that also be causing a bladder irritation? I also just had an IUD removed which I'm sure caused an irritation to my bladder as well.
What’s a good supplement I can take I’ve read that taking an antihistamine like Zyrtec or aloe supplements really help? I would prefer to keep the cost as low as possible
I have to disagree with the pelvic floor physical therapy. My Dr wanted to try and massage my pelvic floor muscles to see if that would help. Let me tell you. I had a charley horse in my vagina for over an hour and very very painful. I would suffer with the pelvic floor pain first!!
Interesting that nothing was said about a significantly difficult side effect of Amitryptiline - it causes urine retention and difficulty urinating. I would love to use it, since anxiety, for me, creates body tension, which interferes with urine voiding in a significant, painful way. But how can I use this drug when it seriously affects bladder function in this manner? So many drugs cause difficulty with urinating, especially muscle relaxants and pain killers. So I am left to manage the horrible pain and malfunctioning bladder anxiety day by day, hour by hour without any helpful drugs.
I think most people could probably use it but maybe have blood tests I used very small amounts and after I stopped blood was normal so just worth keeping a eye on. Some people use huge amounts I have read on the mb
The last 10-12 years of my life have been controlled by IC. The pain at times is so severe, I just want to put a gun to my head and end it. It affects all parts of my life, from my marriage to socialising with friends and family. I have tried so many different medications and none seem to work. I've tried changing my diets with very little difference. I would love to hear from anyone who's managed to control their IC as I'm willing to try anything. I've been taking Elmiron for the past couple of years, plus strong painkillers but over the past few weeks, the symptoms have got worse. I've seen different urologists and they all seem a little lost as to what's the best course to take. I'm a man and to me, it's the worst pain I've ever experienced when it's at it peak. I would love any advice as I'd rather not go down the route of choosing the ultimate cure!! Thank you.
Hi what works for me is .625 MG of Premarin. The bladder needs hormones to function properly after menopause. I am morally against the production of Premarin but I was desperate.
hey,i have ic and when i go to gyneco and do the test they found mycoplasma and ureaplsma and candida...so i m 100% sure that mycoplasma ureaplasma and candida are connect to ic
What's that?? I went on antibiotics like 3 weeks ago and still have symptoms. The issue it seems is that no Dr knows anything about it and even my results are confusing. For example, my uro didn't know what ureaplasma or Mycoplasma was but found it in the system. Then another Dr called to tell me I had an infection. But when I got retested the results were blurred and the other uro in the office told me she didn't think ureaplasma was a thing. It's all so confusing
I am going through something the hospital says is typical UTI. Doesn't seem much like it. Usually on the very rare occasions i have had it, it goes away in 24/48 with really minimal discomfort and no trips to the Dr. This started with antibiotics for bronchitis! It's alarming, none of the UTC antibiotics seem to work in fact, I am worse now than when I started taking them. This is all very confusing. I have been led to believe that lemon juice is good, ACV is excellent, vit. C likewise. Don't seem to be able to buy unsweetened cranberry juice, so i avoid that. I take Bicarbonate of soda. I absolutely avoid sugar, but sounds like you are using it to sweeten drinks. Is there any way out of this nightmare? Its SO debilitating.
Gill, what do you think of taking Nitrofurantoin 50mg (bladder specific antibiotic) for life? I have had IC with Hunner lesions for 21y. It has really helped for pain and F&U in the last year (I was bed ridden), but I nervous about taking it forever. Thank you.
Louise, I took Nitrofuratoin for my I.C. too and yes it does help. I was also told it's not something you should take long term however, I know us I.C. sufferers would do about anything just for a little relief!!
I waited through all this to see if you addressed the actual issue with IC- if you only address bladder and pelvis you are not addressing IC in full because it comes with a syndrome of fibromyalgia, migraines, chronic fatigue, nocturia, etc.. In Canada it is recognized as a symptom of Lyme disease- no frankenstein treatments of the bladder and pelvis address the whole body issue that is IC
You are referring to IC subtype 5 in the Payne subtyping system… aka chronic overlapping pain conditions which has changed dramatically since I filmed his video. Discussed in depth in our live support group meetings and I do hope to make more videos on this too.
@@icnjill Giving subtypes was not mentioned back when I was diagnosed and most in the support group had the whole body issues, and diagnosis with cystoscopy. Now, I go into online support groups with people who have never had a cystoscopy that say they were diagnosed with IC- very confusing.
Thanks for this, is decaffinated coffee okay? and I had acupuncture, which involved a needle in my ankle, and it was attatched to a small machine ,which was charged up, must say it worked while I was having it, but once the course stopped it came back. I am interested in why the pelvic muscles can be too tight?? I thought the idea was to make them tight??
If you use prelief often it can give you kidney stones.I solved this problem with stone breaker supplement and baking soda. I Also, drink lots of clean water. I use zero water. I drink fresh organic juice made with beets, carrots, gala apple, kale, swisschard, and celery. Since baking soda can affect your blood pressure. That the reason why I drink juice and do coffee enema it keeps my BP.low. I have been using cystoprotek for 10 years, and it did help me a great deal. Also be careful with nightshade veg. Yoga excersive especially the one that concentrates on working you're pelvic also help greatly.
how do you eliminate the risk of hairfall while taking Elmiron ? Is there any supplements to help reduce the risk of hair fall that are bladder friendly?
I have bladder discomfort that comes and goes..seems to be related to stress...also had no problem until ended menopause...coukd i have ic..no urgency.
hi, I am not dignosed with IC yet, but i have all the symptoms . I am very affraid of Elmiron and being an algerian woman , i can nor get it here , nor afford it online :( .I have a question: are supplements really prposed as a therapy by the AUA. I cannot find it on their internet page and it worries me a bit. would you mind posting a link i to their recommandations , please?
Hi Jill, I've been having manageable symptoms with lifestyle and diet controls and physical therapy for about 5 yrs. A routine urine test lay week showed blood so my urologist, who appears to have a wonderful reputation here in the UK has said I need a cystoscopy and hydrodistention, and then likely treatments by catheter. I'm terrified that the cytoscopy will make things worse and irritate things much more than they already are. I'm also concerned by urethra damage by catheters. Is there an alternative to the cystoscopy with hydro? Should I opt just for cystoscopy simply for diagnosis? From what I have read is not as effective as diagnosing? However I'm very much against the hydrodistention. Thank you Jill, you're very knowledgeable and helpful. Melissa
Melissa Higgins hi there. I have had both treatments. I was awake for my first cystoscopy and asleep when they did it a second time along with the hydrodistention as well as stretching my urethra. Although I did get some discomfort after each procedure due to the catheter being inserted, it didn’t make things better or worse long term. You must remember, they are professionals and know what they’re doing. They know how to insert catheters correctly and know how much the bladder can take. You will be in safe hands. I agree to everything they offer because if I don’t, they can use it against me later on when something else doesn’t work; “oh well you refused to try this so we’ll never know...” I personally would recommend doing both. You’re already there on the table (so to speak) and it saves you from potentially having to go through it again if they don’t come up with an answer - I’ve also been in that position. I had to go through it more than once due to incompetence of my first urologist. Stretching of the bladder helps with retention of urine and helps with frequency and many other things (or so I was told). Although it didn’t help me, apparently it has helped others. It didn’t make things worse for me and at least I tried it so it’s there in my notes should the idea of the procedure ever come up again. Regarding the blood in your urine, that indicates an infection. Perhaps you should be put on long term antibiotics? Your urologist knows better and if going through it gives you an answer (and potentially some relief with symptoms) then why not? I highly doubt it would make things worse in the long run, you may get an infection from the catheter which happens a lot with me, but you may get a diagnosis and closer to the correct treatment you need. (Ps. I live in Scotland) Hope this helps x
@@kellie4225 Sorry to meddle, just found 2 natural remedies that have helped me I would say 40% and they are Turmeric and Neem in an empty stomach. Best of luck
Bridget be careful of to much calcium or you will get kidney stones like me 17 years of IC talking. : ) well at least we can pee as we swim in the ocean and get exercise. Peace And remember YOU are not alone we are a Family.
Kimberleigh Munn Try D-manose . I can’t cope with muscle relaxers or amitrypthiline ,I get irregular heart beats and feel like I’m getting heart attack .. natural remedies works sometimes followed with pelvic floor exercises
I am on D-mannose. You can buy them on Amazon in tablet and powder form. They have helped so much! You can take up to 6 per day and is derived from plants. I take one per day plus any others when I have a flare up. My support group recommended then to me a few years ago and I have them on subscription! (I’m in Scotland). Hope this helps!
Sophie Wright I’m also from Scotland Attending Ayr Hospital Under Mr Meddings having a really bad time of it with my IC , I’m trying D-Manose and Prelief Marshmallow root Hospital doing instillation (Cystistat but sorry to say I’m still suffering
@@margaretmeechan9490 Margaret how have you been doing, Have you tried Elmiron, It takes a month to get some relief, the bladder installation didn't do anything for me. Stay away from Mayonnaise it has raw egg in it and it will ruin your day, no cinnamon, nutmeg, or allspice But we can pee in the ocean all we want and get our exercise.. Be strong, April 9 will be my 17th year with IC and boy have I seen the quacks come and go. Peace and God bless.
I have a question that nobody has brought up. I began using Pyridium (Azo-Standard OTC) for bladder pain during an UTI as it stopped the spasming and pain associated with that. So when the tests began to come back showing no infection and I realized my IC had come back. For me a natural reaction to being catheterized during a life-threatening illness, but any catheterization created further damage on my severely scarred urethra, thus my IC, which had been in remission for 30 years, flared up and has been back intermittently for about 6 months. Anyway, because catheters, no matter the cause, always seem to do further damage, I mostly avoid treatment and/or further testing if it requires catheters. So I've been continuing to use Pyridium for pain and spasms--it doesn't help urgency or frequency for me, but those I've gotten used to--without any other treatment, or even a firm diagnosis. Is this dangerous? My PCP says it's safe, and didn't dispute my refusal to referral to a urologist. He knows that I know my own body quite well, thank you very much, and when I decide a treatment or referral is not in my best interests, there's little he can say that will affect my decision. All I want to know is if taking Pyridium about 3-4 days per week, once or twice per day, indefinitely, is dangerous? BTW, my injury was caused during a childhood catheterization by an idiot who somehow managed not to officially flunk out of medical school looking for stones, which I had. This was so many years ago that catheters were metal, and he injured my urethra first with the metal catheter, and second, forcing me to pass the stones naturally, and then when they got stuck, using a metal catheter, AGAIN, to force them out. All this with no pain medication, of course, since children "don't feel pain," or so my mother was told, despite my screaming hysterically. I am going to try the OTC meds, though. Where can I get Prelief? I've never heard of it. Thanks!
Sherry, most pharmacies carry Prelief. I tried every prescription, all the bladder installations, diet change ect. I found prelief and cystex to work great, better than any prescription that I took. Pyridium is NOT good for your bladder if taken more than 2-3 days. Most physicians will tell you that and it says it right on the bottle. I get pelvic floor pain, bladder pain, frequency and urgency EVERYDAY and I don't get more than 2 hours of sleep at a time ( i'm up 4-5 times a night to go to the bathroom) I have noticed I have been eating cinnamon buns for the past couple of weeks and I think the cinnamon in the buns is making my symptoms much better!! Bananas help calm the bladder down also!! Good luck!!
You can order prelief on Amazon, or purchase it at Walgreen. I use cystoprotek for my urethra IC and it help alots.Also be care full taking prelief if you a prone to a kidney stone. They a supplement that helps with stone it's call stone braker. you can purchase it at Amazon.
Stay away from Mayonnaise it has raw egg in it and it will ruin your day, count your water intake, have you tried Elmiron it takes a month to work but it helps me, stay away from cinnamon, nutmeg and allspice
Is it possible to have all the symptoms of IC that I had 11 years ago and have it return after 11 years that last about 6mo? I have had pelvic floor exams ultra sounds done on bladder & how it empty’s etc..My MD believe it is IC where urologist feels further testing would have to be done before he could say that is what I had. No medication was ever given except Prelief over the counter which did help…no matter what diet I was on did not help seemed to have to run it’s course thank God I have been pain free for several months ...But the last time i had this was 11 years ago have you ever heard of someone that had it like this? Thanks
You should watch our last video on the subtypes of IC. Basically, we no longer think of IC as a bladder disease... but more of a pelvic pain syndrome or injury. Why? Because it's clear that more than the bladder is involved in MANY patients... such as the pelvic floor muscles, bowel, nerves, etc. So... I think it's very helpful to think of it as an injury and, yes, your bladder OR muscles can be injured again. The fact that Prelief helped suggests that your bladder wall had been injured/compromised in some way and that it has healed well. But, like many of us, it can be hurt again. Remember too that as we get older, our bladder loses some of its ability to protect itself.. thus becomes more vulnerable to certain strong foods like coffees and green teas.
My bladder got i jured in a head on wreck. 2006, Its huge. And it feels like my insides are falling out The urlogest said i need to pee more. Ive been suffering greatly
i am consider i don't drink coffie or pop or anyother acids its been 13 years i have tried every thing i am on elmiron i have seen three bladder doctors in past three years. i did pt i am going to see my forth doctor.
Not directly though I do know that many patients have used MMJ very successfully and that IC is listed as one of the conditions that MMJ can be used for in a couple of states where it is legal.
I had breast cancer 5 years ago which was hormone receptor positive. I will finish the 5 year prescribed Arimidex medication at the end of September. The Arimidex blocks the estrogen production in my adrenal glands so therefore I have not had the hormone for the past 5 years. This has caused a significant problem with my IC which presently is in a major flare. My urologist wants me to use estrace cream NOW to help my IC. My oncologist says NO, NOT NOW OR AFTER I finish the Arimidex in September. I really don't know which way to go. Presently I am fighting an E coli UTI and going for 5 days to an infusion center for Rocephin IV's. A nurse I spoke with there said my body will produce very little estrogen once I'm off the Arimidex because of my age. So what hope is there for me at this crossroads?
diluted Cranberry juice helps for me including avoiding triggers like coffee, tea, chocolate, tomatoes....also avoid sugar and simple carbs like white flour.
I have IC, i have changed my diet and tried including alkaline to my diet and I still suffer from uncomfortable symptoms, they aren’t as bad as they are when I don’t eat certain foods, for someone with IC who doesn’t want to live the rest of their life with painful symptoms removing your bladder should NOT be something that is not an option unless you have destroyed your body with these barbaric treatments like distillation
Omgosh, it is absolutely heartbreaking to see so much pain in these comments. Please be strong! There is reason to believe that help is on the way... there are still clinical treatments being investigated... not to mention the incorporation of AI in the pharm. agency will speed up the devolopement of medication for chronic illness like this one as well. Additionally, companies like Axonics offer sacral stimulating implants that numb bladder pain and urgency
Jill, I have gone through every step available. I'm at the point of pain stim, or pain pump. My doctor rejected my cystectomy request. What do patients like me do when a doctor rejects your request? I'm in CA, do you know of any surgeons who do not dismiss IC patients?
+Jill Osborne thank you, I really appreciate it. I have my own RU-vid on IC so I've been sharing this with everyone. It's been quite a battle. I'm going to call you!
Hey MissM. My mom dislocated her hip when you called, hence the urgent yells in the background. She's still in the hospital but we hope to bring her home either tonight or tomorrow. Thank you for understanding! Hopefully I'll be here tomorrow!
not discrediting all the valuable studies and research into ic but i cured my own ic and medical treatments did not work only temporarily improved symptoms. i believe ic is caused by a fungus/yeast/bacteria that has escaped from somewhere else in your body and has housed itself in your bladder due to a low immune system causing the bladder to be irritated and excessive urination as your body wants that stuff out of there but is too weak to fix itself. i cured my ic by taking strong probiotic supplements (2-3 times recommended dosages) for 12 months and following ketogenic diet (no grains) i ate avocado tomatoes banana because our body needs those things! the ic diet made me sicker because of all the excluded foods. probiotic pills made me flare for about a week after starting them as guess what your immune system is finally getting back missing or low bacteria so its fighting like crazy to get that gunk out of your bladder. after a few weeks i then doubled the dose same thing flares for a week but then felt better then tripled. i was on 90+ cfu per day. i followed ketogenic diet (no grains or starches) to allow my immune system to focus on fixing my bladder and not being bogged down all day on my digestion. it takes time give yourself 1 full year. you do not have to live with ic or accept it as a life sentence you can drink coffee again you can enjoy alcohol again. do not let it ruin your life. i am not a doctor at all but i insist please please please stick with probiotic supplements even if you flare initially for a week or more. each time the flare passes you will feel better and better and get terrific sleep and great sex again 😉 peace out. ps i am not a doctor just an individual who has cured my own ic from lots of my own research.
Graham Langley , Hi please can you list which Strains of bacteria where in your probiotic capsules? So many over the counter- probiotics, but the strains vary . Thanks :)
My wife has been diagnosed with IC at the age of 26. Her doctor now wants her to take a medication that could cause her to lose her hair along with applying a catheter every day for the rest of her life. What can she do?
Jeremy English elmiron might be helpful to stop the pain after 6 months of use. There are natural treatments like marshmallow root and msm suppliments. Please ask if you have questions.
The best book for treating IC is by Diana Brady. The book is called IC NATURALLY. She has helped thousands of women and men worldwide with her natural approach to treating IC. Diana was named WOMAN OF THE YEAR for 2013 and 2014 by The National Association of Woman for her work in treating IC. Her book is available at Amazon Books.
Andrew, lots and lots of water or you'll get kidney stones like me. Did you try Elmiron yet, it took me a month to fill some relief. Peace and God bless.
@@brot5246 Tried Elmiron for a short period, found best results with diet and lots of water. I also take Hydroxizine and Cardura. Elmiron was pulled i believe.. www.levinlaw.com/elmiron-lawsuit Elmiron Lawsuits - Pigmentary Maculopathy The Elmiron lawsuit claims that long-term exposure to Elmiron causes maculopathy, an eye disorder affecting the macula (central part of the retina) and a major cause of blindness. Our law firm is representing individuals who took Elmiron and have suffered maculopathy or other serious eye damage.
that's not clear, cause apparently lemon becomes alkaline in the stomach, but just in case, stop it for 3-6 months. No lemons, oranges, pineapples or vit C.
No Mayonnaise either because it has raw egg in it and it will ruin your day, no cinnamon, no nutmeg, no allspice, Don't you hate stopping a movie to go pee (every time) Or waking up to go pee... Or never ride a roller coaster ... But we can pee in the ocean whenever we like... God bless.
she is an MD, right... 10 different chemical pills , nobody knows how they all interact with each other, side effects that might be worse than the pain
Martha Quintana yo tengo está enfermera y no ay cura tienes que haces dieta no beber nada asido no chile picante no tomate no soda es malo cafeina no café estoy viendo especialista y me recetó trospium colorida 25mg y la otra es elmiron 100mg pero el dolor nunca se a mi doctor familiar me recetó para el dolor gabapentin está es para la ansiedad porque está enfermera está conectada com el cerebro necesita estar relajada tranquila también me mandaron a físico terapia ejersicio para la pelvis y vagina me an puesto tratamiento adentro de la vejiga que le día en resquio pero no miro ningun alivio un día después que tengo sexo es un dolor desesperado por 3 día también te puedes poner almuada eletrica de a los en las parte de abdomen o bejiga te bien estuve en tratamiento por 6 meses para prevenir infecciones de riñones que estaba teniendo cada mes yo me siento que no tengo vida normal com está enfermedad es horrible
Martha Quintana sabes la señora está hablando que ella padese de esta enfermedad y dice de las dietas tan bien dice de físico terapia los tratamiento que ay en los Estados Unidos ay muchísimas personas com está enfermedad
Eliminating all salt from my diet is the closest thing to a complete cure I have come across. That means for the most part you have to carefully prepare all your own meals. I also quit eating meat, poultry and diary products. Salt is your enemy even when it occurs naturally in food. I am now not taking any type of medication for IC. I don't need it.
stephanie renee I have IC and when they use lidocaine in my bladder I have a sensitivity to it so I know Botox will probably cause me severe retention - so what positive effects did you have after getting Botox ? I was going to look into it
@@kellie4225 no ma’am nothing has helped and my urologist has said Botox will leave me unable to urinate on my own more than likely and I was told Botox doesn’t take the pain away - has it helped you ?
Years ago you use to promote the natural approach to treating IC like in Diana Brady‘s book IC Naturally. Now you are promoting drugs and evasive treatments for people. The only step that is worth trying is step one. The rest of the steps are expensive and evasive and you should be ashamed of yourself. Seeing a PT might be good but massage therapy would be beneficial also with a properly trained therapist.
Jill, What can you do if you have the bladder wall injury subtype? I've tried many treatments and have been successful in managing pain and spasms, but I still have small capacity because my bladder feels stiff or rigid. Is there anything I can do about that? I am still suffering a great deal because of it because I can't hold urine due to small capacity.
The AUA Six Step Treatment Protocol is perfect for bladder wall injury.... but that bladder stiffness can be challenging. If you aren't struggling with pain, then many doctors would suggest the bladder holding protocol to help improve your capacity.
