Has anyone ever suffered from urinary incontinence(stress incontinence) before their first child AND pregnancy?
I am 22 years old, first time pregnancy, 39 weeks. Completely healthy other than this one problem that i have had my entire life. Ever since I was a baby I have not been able to control my bladder when I laugh. Almost every single time I laugh I wet my pants...its very embarrassing...Throughout my life I have been very ashamed of this issue and honestly have tried to hide but as I have gotten older it continues to get worse. I know have to wear pads whenever I go anywhere where i think i will laugh otherwise i soak myself through my underwear. Most doctors think it is stress incontinence. They say because I have trouble relaxing when I use the bathroom I do not empty my bladder all the way and have urine left over, hence why I have to use the bathroom every 20 to 30 minutes. Naturally being pregnant it has just gotten worse. No one can give me a REAL HONEST answer on whether or not my problem will get worse if I have a vaginal delivery I would like to have a vaginal delivery but only if my problem is not gonna get way worse. Im already in pads I dont wanna be in diapers and I only have a week left. I have scheduled the C but the doc says it up to me....NOTE: I have seen several urologists and because I have no definitive diagnosis none of them can recommend for or against the C section.
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I was diagnosed with an extreme case of RLS and have been taking Requip along with Klonopin, I am up to 2 mg of Requip 3 times a day and it worked great for a while. It seems like it quit working, my legs hurt so bad I could cry, the weight of a blanket feels like a two ton weight on them, they feel like they on on fire, and and I haven't sleep for days. I just started taking gabapentin, I really don't like taking it because it makes me feel looney kind of like in a fog. Sometimes I break out into a cold sweat so bad that I am just dripping with sweat and feel like I need to lay down, and turn the fan on me. The sweats are beginning to be more often. I just don't know what else to do.....
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I was diagnosed w/ Metabolic mitochondrial myopathy over 10 years ago. Right now I am struggling with the worst illness I have ever had. Started about 5 weeks when I woke up I noticed every time I breath in it stinks. Since then I have gotten weaker and very sick. I have bouts of vomiting, diarrhea, constipation, my head feels full, burning pressure in my ears and sinuses. My shoulders hurt so it feels like my arms will fall off. I also am having problems with this weird pain in my back & stomach, it feels swelled and I feel raw all the way down to my bladder. At times it feels like burning raw sensation all over. My face feels numb and my left foot. I know this makes me sound crazy, it is making me crazy but I just can't seem to will myself to get better. Every day I wake up with some hope and it's the same thing every day. All I have had was a z pack of antibiotics witch seemed to help a tiny bit,(I am able to sit up a little longer)but I can't stop feeling horribly sick & weak.
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Yes, I successfully cured/healed RSD! It is possible!
I effectively "cured" RSD with holistic treatments. I encourage anyone who suffers with RSD consider the holistic regime I created for myself. You can do it too.
Brief explanation of my RSD journey:
Once, I, too, suffered severe Type II Reflex Sympathetic Dystrophy to my right foot and entire right leg up to my hip which presented itself after auto accident injuries stemming from both fractures and a ruptured plantar fascia in my right foot.
I was fortunate I had an early diagnosis (from my Chinese Doctor, who called it "nerve damage" and was first to diagnose RSD. Only because I was "pro-active" and pursued another opinion regarding my symptoms outside the closed box of conventional/allopathic medicine, which was the only treatment medical insurance will pay for.
After my initial nerve damage diagnosis, I brought this vital diagnosis to my allopathic doctors (who actually missed diagnosing it despite my detailed description of the pain and symptoms) who then concurred with my Chinese doctor's diagnosis and for the first time in my life I heard the words Reflex Sympathetic Dystrophy or RSD.
I refused allopathic treatment of RSD (4-6 "nerve block" treatments were recommended to begin by several MDs, including anesthesiologists, sports medicine doctors and Podiatrists). Why? Intuitively speaking, I considered the nerve block procedures to be far too invasive and risky, and which required general anesthesia (additional risks), the use of a fluoroscope (unhealthy exposure of radiation), injections of cortisone and a long acting local anesthetic marcaine, and worse, the end results were NOT at all promising.
Instead, I committed myself to a more holistic approach toward healing because I trusted the wisdom of the body's ability to heal.
Immediately upon my nerve damage diagnosis, about 6 weeks after the auto accident, I began my daily regime of holistic treatments, which included acupuncture, naprapathy, osteopathy, physical therapy, physical exercise physiotherapy which I did for the next 6 months. (As a precaution, in case I did not gain immediate results from my holistic regime, I did arrange advanced appointments with an anesthesiologist to perform nerve blocks. However, I later canceled these appointments because I began to gain positive results relatively soon after I began my holistic regime to heal RSD.
After the first six months of intense daily regime of holistic treatments, my acute and horrible symptoms slowly began to disappear. Gradually, the dark reddish-brown discoloration of my foot and leg began to fade, the inflammation/swelling slowly began to reduce, and the distorted and abnormal shape of my right leg and foot improved (which my husband likened to a "slab of red meat" that "looked like something hanging in a butcher shop"). The over the top excruciating nerve pain (which was off the charts, not in the 1 to 10 range, when asked I rated it "100+++!") to the slightest touch or even a sheet touching my foot was far too painful to bear, slowly began to dissipate into the 1 to 10 range. The complete loss of normal ambulatory function with my right leg and foot (I required a wheelchair or crutches to hobble around on my left leg) began to slowly improve after much treatment and with my determination to be pain free, to walk, run and dance again, I "pushed through the pain" with the physiotherapy machines and "re-learn" how to walk again. I literally reprogrammed my brain to walk again.
About six months into my holistic regime, I was again able to walk on my right leg and foot without the aid of a cane or crutches. However, each time I flexed my right foot to walk, it was painful, far too painful to walk long distances. I rated it an 8 on the 1 to 10 scale when asked by an anesthesiologist which I deemed completely unacceptable live with the rest of my life.
This anesthesiologist, with whom I had a 6 months post-RSD diagnosis exam (for medical insurance purposes) was the director of the pain clinic at Kaiser Hospital in Sacramento, CA. This anesthesiologist, who would have otherwise performed nerve block treatments on me had I surrendered to them, wrote in my medical records, "patient sought alternative treatments with acupuncture, osteopathy, naprpathy for treatment for RSD and achieved remarkable results..." My Kaiser podiatrist wrote, "patient had miraculous recovery from RSD with holistic treatments..." My Kaiser internist, my private St. Francis Sports Medicine, a medical doctor, my Kaiser physical therapist all wrote similar comments in my medical records which not only validated my intuition to take the risk to explore holistic treatments but provided substantiation that they were effective and beneficial which forced my Farmer's Auto insurance company to eventually pay for my holistic treatments which were all rejected. Two years later I was reimbursed for all my holistic treatment costs.
I want to offer another perspective into the closed, blocked mindset dogma of allopathic medicine and doctors. During my final exam with the anesthesiologist(as previously mentioned), although this doctor was quite expressive about her amazement of my then-recovery with RSD, she still remained stuck in her dogma when we discussed my pain level. She actually told me that I had reached the limitations of any more recovery because I had passed the 6 months window of time for nerve damage. She said, "I am sorry but I am afraid you will have to learn to live with the pain."
This director of Kaiser's Pain Clinic which treats RSD patients continued to reinforce her assessment that I would not improve, that I reached the limits of any possible recovery. She told me how lucky I was, how much better off I am than most of RSD patients who never get better and only worsen, etc., and I assumed she meant that I would waste my time and money if I continued with holistic treatment.
She shook her head when I told her I wanted to continue with acupuncture treatments until I was completely pain free. She may have meant well and didn't want me to have high hopes of recovery and then experience failure, or whatever. This anesthesiologist, who performs nerve block treatments, gave me all the information of what she knew based upon her 20+ years of experiences with RSD patients.
Fortunately, I did NOT accept her prognosis. Instead, I passionately said, "Doctor, I trust the wisdom of the body to heal and I shall continue with acupuncture treatments until I am completely 100% pain-free. I'll be damned if I willing to live with this pain and can't go for long walks, run or dance the rest of my life because a jerk ran a stop sign and plowed into me!"
Her expression spoke volumes. She was a bit astounded by what I said but not one word of encouragement was spoken. There was a long uncomfortable pause between us. Finally, I said, "One day I will return and prove to you that I am pain free and then you can bring in an acupuncturist, a naprapath, and an osteopath into your pain clinic to help RSD patients.
It took another six months of treatment before I was completely pain free and before my right leg matched the color and size of my left leg. My internist/primary doctor was thrilled by my recovery and accredited it primarily to my "positive attitude and determination." Kaiser wasn't interested in accepting my recovery was due to holistic treatments. Instead, it was just considered "miraculous" remission of RSD which, of course, does NOT give any credit to all the beneficial holistic treatments I had.
I am still pain free after 11 years and walk miles daily and go dancing twice every week. I am grateful for all of my holistic doctors, I hope my allopathic doctor learned from my experiences and success with curing RSD.
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The bottom of my feet have been black for a few months now. Why is that? What is causing them to do it? I am 37. I so have chronic anemia and just had a blood transfusion a couple of months ago. I also have nerve damage in my neck and right shoulder that causes my hands to go numb and I'm noticing now that the palms of my hands are turning black as well. Should this be taken seriously?
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Has anyone had an exploding abscess in a pouch,? Did the medicals
tell you why and what caused it. ?,Or did you get the Mushroom treatment ?
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i was diagnosed 2 years ago and since then i have been on methotrexate but since that hasn't worked i have recently been put on sulfasalazine which i take four a day and am still on 6 methotrexate a week. i am hoping this is going to work but since i have been on this i have been having bad side effects such as really bad head aches, dizziness and feeling sick all the time and lack of appetite so hopefully that will die down over the next few months. the only thing that i have found when feeling sick is by having zantac as it helps settle the stomach.
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Does anyone have information about this type of angina? Mine is quickly getting more aggressive in nature and my most recent episode two days ago caused me to nearly pass out with the pain. I do know that it is caused by a spasm and it is generally considered a benign condition, but it is not feeling that way anymore. Please share any real knowledge you may have on this topic with me. I really hate to call the emergency services if there is something else I can do to alleviate my pain beyond using my nitroglycerine spray and chewing the aspirin.
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