Multiple sclerosis symptoms in dogs

Common Questions and Answers about Multiple sclerosis symptoms in dogs

multiple-sclerosis

Stress regulation in multiple sclerosis-current issues and concepts Mult Scler 2007; 13; 143 originally published online Jan 29, 2007 C Heesen, D C Mohr, I Huitinga, F Then Bergh, J Gaab, C Otte and S M Gold "An increasing body of empirical evidence now supports the association between stressful life events and relapses in MS, although this literature is of varying methodological quality and does not permit causal inferences.
My balance as a kid was the best in my gym class - I was schooled in the UK for awhile. I have mild symptoms of PTSD which are exacerbated by stress but these have been treated. I am not in denial about the effects of stress from witnessing domestic violence since I was age 5 - and then having a life that repeated some of those aspects. I learned to rescue my mom my whole life which she was glad to take advantage of but abusive of me emotionally and sometimes physically.
fast forward a few years (i am having major memory problems) about 6 years ago after bouts of the above you can add the following, they have either came back or become more severe and/or i have developed new symptoms, i know you are not doctors here goes, i can be ok one day and be in severe pain the next .................
Brain tumors, multiple sclerosis, epilepsy, chronic fatigue syndrome, parkinson's disease, alzheimer's, mental retardation, lymphoma, birth defects, fibromyalgia, and diabetes. Aspartame is made up of three chemicals: aspartic acid, phenylalanine, and methanol. The book "Prescription for Nutritional Healing," by James and Phyllis Balch, lists aspartame under the category of "chemical poison." As you shall see, that is exactly what it is. What Is Aspartame Made Of?
Umm, riddle me this, Batman: Exactly what test are vets using to detemine a positive or negative test for lyme in dogs? Why are the test results for people doubted, but not the dogs? And if they can get a definitive "yes" in dogs, why aren't we "humans" getting the same type of test?
However, I have been in touch with patients with symptoms very similar to mine who got it here in the States. My symptoms mimiced MS and IBS. My coinfection of Bartonella has made the GI and neuro symptoms worse. Joint pain is very common, but is not a required symptom. To me, it makes sense that a different tick can result in a variation of the bacteria that results is a somewhat different disease presentation.
http://www.medhelp.org/posts/Multiple-Sclerosis/symptoms-made-you-a-loner/show/780319?personal_page_id=524391&post_id=post_4067503 the insideous thing about this is no one on the outside can really "see" much of our symptoms but boy do we feel them. i haven't worked steady in two years. I've looked but with the econ and my lack of overall confidence with stamina and the fact i never know how i'm going to feel i don't know what kind of work i can do anymore.
A similar pattern of deficits has been observed in patients with Parkinson`s disease and multiple sclerosis.... ...... Most studies report the resolution of neurotoxic symptoms within 2 to 3 weeks following the discontinuation of IFN-a therapy. However, some patients develop neurotoxic side effects that persist for months or years after treatment discontinuation, without any intervening change in their disease status or the initiation of other neurotoxic therapies....
http://www.medhelp.org/health_pages/Multiple-Sclerosis/The-Importance-of-the-Timeline/show/765?cid=36 Channel those anxieties into useful outlets that empower you rather than drain energy. And let us know how you're doing along the way.
Another condition that presents with multiple areas of sensory disturbances that each last a few weeks is multiple sclerosis MS). If you have not had an MRI of your brain and cervical spine, this would help evaluate you for possilbe MS (although this is less likely). I hope this has been helpful.
I am wondering if a mold/dust allergy combined with a poorly maintained air-conditioning system in workplace could have anything to do with our symptoms? Would be interested in your comments on this.
I was a wreck from all that was going on. You see I joined in Oct 08. The first time I had heard the would multiple sclerosis linked with my name had been in Aug 08, just a few months prior. So I made a profile with no pic and choose the name saveone because I am passionate about saving discarded animals. There is a saying, "Save one until there are none". Now that's my story and I am sticking to it ;0) take care and live well, terry ps.
Doni, thanks for sharing this . . . I too, find the brain very fascinating! Even though I am the “lucky” recipient of a Fibromyalgia diagnosis . . . AND a daily dose of Provigil to go with it . . . I really consider myself to be in limbo. I have multiple neurological "type" symptoms that don't seem to fit and I have been referred to Neuro #3 - - whom I will meet in January.
The doctor added up some unexplained symptoms I'd had in college (vertigo, numbness and double vision)and put it together to spell m-u-l-t-i-p-l-e s-c-l-e-r-o-s-i-s. Of course there were no MRI's back then, but because my symptoms involved separate body systems and separate times, I was given the probable diagnosis. MS was much harder to diagnose back then, but my symptoms fell right for a DX.
58 AM Signed CCHS STAFF PHYSICIAN NOTE OF PERSONAL INVOLVEMENT IN CARE I have reviewed the follow-up note obtained and documented by the advanced practice nurse and I personally participated in the key components and have answered all the patient's questions. 57 year old male with non specific MRI findings which have not changed over time. The etiology of his symptoms is still not clear to me. He has on-going neck pain, dizziness, and poor balance.
http://www.nationalmssociety.org/about-multiple-sclerosis/pediatric-ms/pediatric-ms-centers-of-excellence/index.aspx Now, we here have seen some problems with the Mayo Clinic's attitude toward "adults" with possible MS, I have no reason to believe that the pediatric department would be arrogant and uncaring like some of the adult doctors are. Pediatricians are usually in that field because they truly care about children.
About the blood clot worry----- I truly don't believe you have one or you would have stroked out or been dead by now. (Gallows humor! Forgive me----- but it's sometimes the only type of humor I have some days.) First determine if your MRI was without contrast all the way through the procedure or if just through part of it. Some MRIs are done with no contrast at the beginning and then with contrast through the rest. Now you can see why we keep all our records.
Since then I've noticed it multiple times a day in multiple physical positions. I asked my father who is a doctor and he said it was probably a pinched nerve or something, and didn't seem very concerned. However, he is seldom concerned with my health worries, so I don't really trust him. I'd love to find a list of problems this could be a symptom of.
IS IT ALL IN MY MIND OF BEING PRGNANT OR COULD IT MEAN MULTIPLE BIRTHS THATS WHY EVERYTHING IS SO FAST?
I am not going to list symptoms-it is sufficient to say it resembles some symptoms of Lyme, Chronic Fatigue Syndrome, Multiple Sclerosis. MRI of brain without contrast-found "minutes of white matters" lesions MRI of brain with contrast to evaluate white matters lesions-does not enhance Evoked Potentials test-pretty much ruled out MS-the test result were either normal or negative Autoimmunes--oh, too many to list here, repeat test over and over--all negative or normal.
I have this condition and was diagnosed in the past with multiple sclerosis, fibromyalgia, and degenerative disc disease. There are a lot of neurological symptoms that same people with EDS can have. Look on the website for an article about these neurological symptoms. People with EDS also frequently have spastic colons that result in constipation and loose stools. Many times people have both EDS and fibromyalgia.
He is notably also the only specialist so far to acknowledge what I have been fearing, that my problem might be multiple sclerosis. The others have all dismissed that as a possibility, but have done almost none of the testing that could support such a decision. Their argument is that I am not a classic, textbook case of MS, while admitting that there really is no true classic, textbook pattern of MS.
Hey guys, I posted this in the Multiple sclerosis forum but was advised to post elsewhere too. I have never really had any real medical problems, so this is really scaring me. It started with muscle spasms a little over a month and a half ago. Then one morning I woke up with a wrist that hurt bad when i moved it back or forward. That lasted about a week and a half and within that time I had developed a tingling sensation in my fingers and has spread to my whole left hand.
Lyme Disease is a bacterial infection from a tick bite and can mimic diseases such as multiple sclerosis and amyotrophic lateral sclerosis. IgeneX is a Lyme specialist lab in the US.
org/posts/Multiple-Sclerosis/MULTIPLE-SCLEROSIS-RISK-AFTER-OPTIC-NEURITIS/show/664930 You'll see from reading this, that it's not a given that your wife will develop MS, but that the odds increase on other things identified at the same time. Hope this info helps - thanks for joining us!
This is thought to be caused by low protein called hypocretin, which is made in the brain. The symptoms are an urge to sleep especially after meals. Sleep studies and EEG are done to rule out other causes of poor sleep and insomnia. Eating light and frequent meals during the day helps. Also assigning a nap time during the day often helps. You can take a light meal before this. At times some ante depressants are prescribed to control the symptoms.
I saw a program today where a man's dog has multiple sclerosis and the dogs symptoms sound just like emmitts. Any ideas from anyone on what I can do to find out how to help my little one,Emmitt. I have already spent around $800.00 on him and am pretty much tapped out.
My life is not that much different than it was before surgery. I get tired but also have Multiple Sclerosis. I look younger than I have in years. No one can tell I am in chemo right now or even have Cancer. My biggest fear was pain. I have a great pain clinic and they have gotten rid of that fear. I look at Ovarian Cancer as a Chronic Illness like diabetes. I have to treat it but it is doable.
//www.arkanimals.com/service-dogs-for-multiple-sclerosis/ Congrats on the weight loss - that is fantastic. I sure understand your concern about the weight gain on IVSM. I'm with Shell - be sure to talk to your doctor about this. Too late for IVSM? I don't imagine so, because it can still help to give you relief to the inflammatory part of your symptoms. Yep, you've been AWOL from here for a while but that is understandable.
I know it is hard not to worry. I am a pro now with Multiple Sclerosis and Cancer. I worry very little these days. I have a good Primary Care Doctor. I let her worry for me. She is a good liar. I ask her if I should worry and she says "No". I can tell when she is worried. Keep good notes of symptoms. I was told I had cancer three times and some other nasty diseases and they were wrong. I do have cancer now. I have been diagnosed for a year and a half.
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