General :: Sensitive Gag Reflex
Mar 2, 2015
Ok I'm 19 years old and I think my health is good. Anyways, my gag reflex started one day after I was eating and I just looked at the food I was eating and suddenly didn't want it. At first it was just when I would brush my teeth and after using mouthwash, I would usually cough and heave or spit out water. And now I have noticed that after I eat, I can feel my gag reflex. Like I can feel that there is food stuck there (it's probably not, but I can feel something nasty there), and one time I touched my throat (outside neck area) and I wanted to vomit. Now I have an issue sometimes with the front of my shirt collar touching my neck area, because I feel suffocated and it makes the food feeling even worse.
I do salt gargling sometimes, but I still have it! Any help? I also get stomach aches more frequently now (I have gotten 3 so far in these past months and have thrown up.)
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I am a 42 year old mom of 2 boys. I have been healthy most of my life. In 2011, I noticed some numbness in my left hand and it seemed to be "clumsy". My mom has MS so it scared me. Considering my family history, my family doc sent me to neuro and to have an MRI. The MRI and my exam turned out to be normal. The neuro said it could be my ulnar nerve. 2012, another episode and this time with worst headache ever and blurred vision. Once again I checked out fine. Then in July 2014 while on vacation, I became dizzy and started to stagger. I went to an urgent care and they told me I had vertigo. After that the vertigo/clumsy remained, and I started having myoclonic jerking of my muscles and headache. I was checked by neuro when I got back from vacation. The vertigo went away but muscle jerking remained. Normal exam and bloodwork. August 21, it came back the vertigo/clumsy feeling, headache, my legs being sensitive to touch, and I occasionally repeat things when speaking like my brain can't remember. I went to a recommended neurosurgeon. His exam revealed Babinski reflex, Hoffmann reflex and brisk reflexes. It was symmetrical on both sides He ordered an MRI. I couldn't get in for almost 2 weeks. The waiting is making me crazy.
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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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My sense of smell is so sensitive that I've had to ask my husband to change his deodorant, we've changed our laundry detergent to one without a fragrance, and if anything is seasoned with Italian herbs or herbs in general I become nauseous. Is anyone else sensitive to smells?
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I am a 54 year old female who has suffered from migraines most of my adult life. Smells have been a trigger for them. Lately I smell things no one else does and always followed by a migraine.
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Ever since I could remember the tip of my penis has been very sensitive to touch, even if I realize that uncircumcised mens' penises are somewhat sensitive to the touch, mine is like borderline impossible to feel without getting extreme discomfort. It's also quite reddish almost all the time. For quite a few years I know I wasn't cleaning it properly, and up until a couple years ago I know I had some smegma under the foreskin that I was too hesitant to peel off due to the pain. A couple years ago I finally decided to do it and got all of it off, and now I can pull the foreskin all the way back, but the discomfort is still there. I started using a balanitis cream thinking it would help, but it hasn't really done much. Do you have any idea as to what may be going on?
I'm 21 years old right now, if that matters.
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I am a 56 year old who was circumcised three weeks ago.i am having problems because the head of my penis is so sensitive I cannot touch it or wear pants/boxers.tried a dressing but found it sticks so badly its too painful and damaging to remove.i am desperate to get back to work but can see no improvement even after three weeks.
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So my boyfriend has been fingering my for the last couple days and afterwards and during it. My clit will get very sensitive. I'm not sure if it's natural and will go away and be fine or if it's something I need to worry about. Also its very sensitive and can sting when i go pee.
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Ever since I can remember my tastebuds have been very sensitive to taste and to pain. For instance whenever I drink a fizzy drink I have to stir it around a lot because otherwise it hurts to drink it and I can't eat spicy foods without extreme pain to my tongue (even mildly spicy). I can also taste things in food and drinks that others can't, such as limescale in water and pesticides used on vegetables. I was wondering if there was a name for this or if it was a condition or something, also I would like to know if anyone else has this problem so I know I'm not alone.
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I'm 21 and have been sexually active since I was 15. For as long as I can remember, I've had a clitoris that is way too sensitive to touch. It's very easily irritated by my pants digging into it, etc. I ride horses (jumping) and a lot of times I have to wear a pantiliner just to keep my pants from rubbing against it uncomfortably. I can't even touch it myself. The only thing that ever truly touches it is the water in the bathtub.
I've instructed partners (including my current boyfriend) to avoid directly touching it as much as possible. As long as they touch around it, I'm fine and things are great. But if they get too close, that extreme, intense sensitivity ruins the mood for me. It's almost painful, if that makes sense.
(Sex is still very enjoyable for me, so that isn't an issue.)
But is there anything I can do, or is this just the way that I was "wired," so to speak?
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This is my second bout of PMR. The first time I really did not experience any side effects of the pred...with the exception of small weight gain and slightly moon faced.
I have been back on pred for 2 months. Started at 20mg. I am now down to 15 mg. I will be reducing by 1 mg / month until I reach 10 mg. Then I will reduce by 1/2 mg/month.
Anyway, I am having a very difficult time with depression this time. I am usually a pretty upbeat person, but I find myself sinking. I am so unhappy,
I am also starting to have 'mild' suicidal thoughts.. aka maybe I should just take the whole bottle of Attivan. As quick as the thought enters my mind, its gone.
Adding to this PMR...my husband passed away 8 yrs ago. I am now feeling like I did in the 2-3 yrs after. I am 62 yrs old. The only thing that keeps me going are my 9 grandkids. The problem is that I have built my whole life around only these guys. Prior to PMR and pred, I was doing fine.
Anyway...has anyone else experienced this. And if so what did you do?
I keep telling myself to stop feeling sorry for myself and move on.
I have no pain, Thank God. It's just the head confusion, lack of focus and now depression.
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I am really nervous. I am 14 years old and my foreskin has gone off the head and retracted back the way. Now the head is out and it is very sensitive and hurts when anything touches it and I am finding it very comfortable
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Recently, I visited a dentist , and my teeth were cleaned. I was asked to be repeating that every six month. However, after the visit, a tooth became very sensitive to anything that touches it, whether hot or cold, or even ordinary water, a kind of pain sends me jumping.
I went back to the Dentist and he directed for an X-ray on the affected tooth. The X-ray showed a hole in between the teeth(an abscess). Some drugs were given to me( Amoxicillin 500mg; Flagyl 400mg; Cata? 50mg) which I have taken for some days. The pains are still there, and the dentist says the tooth will have to be removed, which I do not like at all! Instead, I have decided to to start brushing my teeth twice a day using Sensodyne toothpaste, and Listerine Mouthwash, twice a day. Doctor, will the alternative procedure that I have prescribed for myself eventually save me from the removal of the tooth, which I very much detest?
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I'm 25 and have struggled with phimosis for most of my life. I had never been able to see my glans before as they were always covered. During an erection I still could not get them exposed and wearing a condom was just so painful so yes, still a virgin at 25.
Recently I went to the doctor and got circumcised to correct this. Its been 3 days now, still have the stitches there and the pain is ok (except for the occassional erection). My main problem is the glans..they are super sensitive,even passing a cloth there sends me to hell and back. And they are bright red in colour and swollen. How can I desensitize them?
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The past 9 weeks I treated with olysio and sovaldi. They stopped at 9 weeks. The test came back at week 8 still positive. Tx was stopped. Geno 1A, Past biopsies showed stage 1 mild fibrosis. In 2010 they didn't get a good sample but told me it was probably still stage 1, but not sure. Now after an ultrasound that's "suggestive" of cirrhosis I fear after failed tx the progression will bring me down even quicker. Anybody have any GOOD info that olysio/sovaldi speeds up the virus progression? Dr.says no. Have been positive for 50 years. Since 1999 I have lived a very healthy lifestyle. For most of the years I supplemented and took the herbs to keep my liver in as good of shape as I could until a "cure" came along. So much for that idea. I never did the interf/riba. The past couple years for some reason I stopped taking my supplements, (glutathione raising supplies etc) I used to be a member of a group that was alternative oriented, then I stopped that. I did the q80 variance test and it was positive, and so I went ahead with the tx. My question is: Is this new drug coming out only for those who weren't sensitive to the q80? Or is it supposed to take care of tough bugs like mine? Im hopeful I will be eligible for the new tx. Im 68 now. I am starting to experience symptoms, unpleasant symptoms. Good days/bad days. Sorry for rambling but I saw Blue Metals comment about disease progression after failed tx and it kinda spooked me.
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My latest lab results read:
TSH with reflex to FT4 - 19.825
T4 free 0.4
I keep seeing a lot lower numbers on this board and cannot find anywhere that shows more info on my numbers.
How bad are those numbers? My Dr just upped my levothyroxine but acted like it was no big deal.
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The neuro scrapped the bottom of my foot and could not get it to jump like it used to. he kept trying but nothing happened. I thought this was important but nothing was said and when I asked my physician, he said this was normal. what's it mean if the foot doesn't react?
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What is this test? I had this test done last month among others and this one came back as 7.46 mIU/L and the reference range is 0.40-4.50 . Dr. Wrote "elevated-over 7."
Also my calcium was high at 10.6 mg/dL and reference range from 8.6-10.2
Free T3- 4.3 ph/mL reference range from 2.3-4.2 , slightly elevated.
T-4, free- 1.5 B&G/dL reference range from 0.8-1.8
My main question is what is the tsh 3rd generation with reflex to ft4?
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I wanted to get feedback on sedation , I get procedures every 10 days for the pain I have my doctors so SGBs on one foot then the other for I have RSD in both feet and the surgeon uses versed to sedate me and I now I've built up a tolerance , they use 4 doses where as when I first started I only received 1 dose but now this last procedure I felt no relief so the sedation is not working and it's very painful to do these nerve blocks without sedation so I'm lost as to what to do I'm considering stopping the injections because of this has anyone experienced the sedation not working anymore and if so what did you do?
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Anyone else with MS have this? I developed pulsatile tinnitus over the summer and saw an ENT recently to look into it further. It's only in one ear, which is coincidentally on the side where I have the majority of my dysesthesia. My hearing was fine, but acoustic reflex came back abnormal and there were no ear issues found, so he ran a CT scan to look for tumors. None turned up, so they are saying this could all be from MS. Seems strange to me, but many things are with this disease. Anyone think this sounds right or should I push a little more for answers?
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In pain after botched bunion surgeries by podiatrist, underwent reconstructive surgeries with OS. Still in pain, now was diagnosed by OS with RSD. 3 phase bone scan showed "increased blood flow and soft tissue uptake in the right ankle and foot. There is intense increased uptake in the right first metatarsophalangeal joint likely represent reactive postoperative change and consistent with postsurgical changes and reflex sympathetic dystrophy in the right lower extremely". Pain management said that as I DO NOT have swelling, change in color and temperature, it is not RSD and sent me back to OS, who already told me that there is nothing else he can do surgically. So I have terrible burning and stabbing pain and muscle spasms. I just want to understand if RSD is a nerve pain or is the result of some abnormal process in bones as was indicated in my test?
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