If you own MS, know someone beside MS or are surrounded by the medical corral I would appreciate any info on MS. My Dr say nearby's a fate that I might enjoy MS. I enjoy trouble walking. Feel unbelievably stiff especially within hips. Right immediately to be exact solely symptoms I own. I hold have a spinal MRI & am going to hold a brain MRI subsequent. I enjoy have several blood test for other diseases such as Lupus and Lyme disease. All test be denial. I am a 47 yr feeble feminine. I be aware of similar to I am contained by pretty moral strength excluding the trouble walking. Are injections not easy to bequeath yourself? Does pills sustain so you can do everyday undertakings? Any info is appreciated.
Answers:
Hello,
I enjoy have MS for lots years..I am 49 F and doing great.I work full time wallow in an busy life span beside my kids and regal kids.
I hold the most adjectives form of MS ,Relapsing Remitting MS.. I enjoy long period beside few to no symptoms.It's be more than 7 years since my finishing exacerbation (attack).
I do steal Betaseron (one if the inject ables) and it's a piece o cake..I appropriate 3 shots a week, respectively one stings for nearly 10 second..that's smaller number than 1 minute a week of discomfort for tons of benefits.
If you are diagnosed next to MS. don't nouns..it's really not that impossible. The treatments enjoy come so far contained by the finishing 10 years.Do your research on which disease modifying drugs fit best into your lifestyle and requirements, respectively hold their own advantages and disadvantages. Stay stirring..yoga is a great exercise to keep hold of you flexible and facilitate near stability, munch through a honourable in proportion diet and stay positive !
Good luck !
I also thought I have LD but be talk out of it by my neuro at the VA. I took alot of doxycycline for a couple of years and quit at his urgence and I agreed because I wasn't getting any better (I'm in a power chair). I was starting to stride near my person on foot and can't any more. Now I'm starting to re-think LD because of the timing. I be origionally on Avonex and consequently Copaxone for 5 + years neither of which slowed down what ever this is I hold. I'm very soon doing Tysabri infusions every 4 weeks. My brain MRIs hold un-active lesion so he desires to see my spine again which be never lit up earlier. Oh okay, a spine cord MRI should answer the LD/MS request for information hopefully. Sorry just about my lacking coherence but the injections didn't work for me and I kept slipping further until I dabble next to the doxy/LD which I might own to check since I'm struggling again. I'm 58 and be properly diagnosed MS support within 2000 (MS be suggested rear as far as '93). The blood test other seem to be to come hindmost denial for LD.
I be diagnosed concluding November, several years after my first symptom, at which time I be also told that I might eventually develop MS.
----------------------
From the first join posted below:
"There are no laboratory test, symptoms, or physical findings that can, by themselves, determine if a creature have multiple sclerosis. Furthermore, in attendance are frequent symptoms of MS that can also be cause by other diseases. Therefore, the MS diagnosis can one and only be made by supportively ruling out adjectives other possibilities.
The long-established criteria for diagnosing MS are:
There must be ambition evidence of two attacks (i.e. two episodes of demyelination in the intermediate timid system). An attack, also certain as an exacerbation, flare, or relapse, is defined clinically as the sudden appearance or worsening of an MS symptom or symptoms, which last at lowest 24 hours. The target evidence comes from findings on the neurologic exam and extramural test.
The two attacks must be separated contained by time (by at lowest one month) and space (indicated by evidence of inflammation and/or sabotage contained by different areas of the interior anxious system).
There must be no other explanation for these attacks or the symptoms the soul is experiencing."
--------------------------
I outstandingly much express sympathy beside what you are going though presently, and I will you adjectives the best. I can update you, from my experience that the solitary predictable entity give or take a few the disease is that it is NOT predictable, but here are multiple resources available for anything an MS paitent might stipulation, and oodles, tons areas of research loyal to finding a impose and an eventual cure MS
Best to you.
Many associates who are told they enjoy MS latter turn out to in truth enjoy Lyme. It's a thorny query. Be aware of a couple of things: lab test for Lyme are disreputably problematic. They normally miss as various cases as they entrap. Also, a brain MRI won't prove anything one route or the other in relation to Lyme. (neither will a spinal hit.) You really should be evaluated by a doctor who is comfortable near neurological Lyme.
Good sources of info just about Lyme disease:
http://www.canlyme.com
http://www.lymenet.com
http://www.lymeinfo.net
http://www.lymediseaseassociation.org...
http://www.ilads.org
http://www.betterheatlhguy.com
http://www.publichealthalert.com...
Below is a knit to an MS-site, which you might find polite. If your MRI indicates that you hold MS, you will probably own to hold a lumbar puncture as okay to further confirm the diagnosis.
The inteferon tablets is used to lower the number of exacerbations and slow the progress of MS, it should not hold an effect on the problems you are already have. There are, however, plenty of other drug and treatments (physiotheraphy), which can address your symptoms - have a chat to your doctor/neurologist in the order of these.
As another answerer said, the injections are a piece of cake. I inject myself once a week intramuscular, it take going on for 10 minutes, including adjectives the preparation. The medication can enjoy some side effects, such as flu-like symptoms, headache etc. which last for in the region of 24 hours. These usually disappear after a while. I judge the majority of patients experience no side-effects after a one year maximum. For me it took longer and I still draw from an occasional lower than the weather year.
You obligation to jump for regular check-ups and shouldn't pinch aspirins or drink hulking amounts of alcohol if you are on inteferon drug (it's complicated on the liver and blood-thinning.
MS is a markedly individual disease and one heaps culture (also those who enjoy no clue) enjoy an belief almost in relation to cures, treatments and the overall progression of your disease - which will usually be a intensely distrustful estimation, because they read this and hear that. Thing is that you regularly hear going on for the worst cases surrounded by the medium. IF you should be diagnosed near MS, afterwards don't frenzy, listen to your adjectives sense and your neurologist/doctor.
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Answers:
Hello,
I enjoy have MS for lots years..I am 49 F and doing great.I work full time wallow in an busy life span beside my kids and regal kids.
I hold the most adjectives form of MS ,Relapsing Remitting MS.. I enjoy long period beside few to no symptoms.It's be more than 7 years since my finishing exacerbation (attack).
I do steal Betaseron (one if the inject ables) and it's a piece o cake..I appropriate 3 shots a week, respectively one stings for nearly 10 second..that's smaller number than 1 minute a week of discomfort for tons of benefits.
If you are diagnosed next to MS. don't nouns..it's really not that impossible. The treatments enjoy come so far contained by the finishing 10 years.Do your research on which disease modifying drugs fit best into your lifestyle and requirements, respectively hold their own advantages and disadvantages. Stay stirring..yoga is a great exercise to keep hold of you flexible and facilitate near stability, munch through a honourable in proportion diet and stay positive !
Good luck !
I also thought I have LD but be talk out of it by my neuro at the VA. I took alot of doxycycline for a couple of years and quit at his urgence and I agreed because I wasn't getting any better (I'm in a power chair). I was starting to stride near my person on foot and can't any more. Now I'm starting to re-think LD because of the timing. I be origionally on Avonex and consequently Copaxone for 5 + years neither of which slowed down what ever this is I hold. I'm very soon doing Tysabri infusions every 4 weeks. My brain MRIs hold un-active lesion so he desires to see my spine again which be never lit up earlier. Oh okay, a spine cord MRI should answer the LD/MS request for information hopefully. Sorry just about my lacking coherence but the injections didn't work for me and I kept slipping further until I dabble next to the doxy/LD which I might own to check since I'm struggling again. I'm 58 and be properly diagnosed MS support within 2000 (MS be suggested rear as far as '93). The blood test other seem to be to come hindmost denial for LD.
I be diagnosed concluding November, several years after my first symptom, at which time I be also told that I might eventually develop MS.
----------------------
From the first join posted below:
"There are no laboratory test, symptoms, or physical findings that can, by themselves, determine if a creature have multiple sclerosis. Furthermore, in attendance are frequent symptoms of MS that can also be cause by other diseases. Therefore, the MS diagnosis can one and only be made by supportively ruling out adjectives other possibilities.
The long-established criteria for diagnosing MS are:
There must be ambition evidence of two attacks (i.e. two episodes of demyelination in the intermediate timid system). An attack, also certain as an exacerbation, flare, or relapse, is defined clinically as the sudden appearance or worsening of an MS symptom or symptoms, which last at lowest 24 hours. The target evidence comes from findings on the neurologic exam and extramural test.
The two attacks must be separated contained by time (by at lowest one month) and space (indicated by evidence of inflammation and/or sabotage contained by different areas of the interior anxious system).
There must be no other explanation for these attacks or the symptoms the soul is experiencing."
--------------------------
I outstandingly much express sympathy beside what you are going though presently, and I will you adjectives the best. I can update you, from my experience that the solitary predictable entity give or take a few the disease is that it is NOT predictable, but here are multiple resources available for anything an MS paitent might stipulation, and oodles, tons areas of research loyal to finding a impose and an eventual cure MS
Best to you.
Many associates who are told they enjoy MS latter turn out to in truth enjoy Lyme. It's a thorny query. Be aware of a couple of things: lab test for Lyme are disreputably problematic. They normally miss as various cases as they entrap. Also, a brain MRI won't prove anything one route or the other in relation to Lyme. (neither will a spinal hit.) You really should be evaluated by a doctor who is comfortable near neurological Lyme.
Good sources of info just about Lyme disease:
http://www.canlyme.com
http://www.lymenet.com
http://www.lymeinfo.net
http://www.lymediseaseassociation.org...
http://www.ilads.org
http://www.betterheatlhguy.com
http://www.publichealthalert.com...
Below is a knit to an MS-site, which you might find polite. If your MRI indicates that you hold MS, you will probably own to hold a lumbar puncture as okay to further confirm the diagnosis.
The inteferon tablets is used to lower the number of exacerbations and slow the progress of MS, it should not hold an effect on the problems you are already have. There are, however, plenty of other drug and treatments (physiotheraphy), which can address your symptoms - have a chat to your doctor/neurologist in the order of these.
As another answerer said, the injections are a piece of cake. I inject myself once a week intramuscular, it take going on for 10 minutes, including adjectives the preparation. The medication can enjoy some side effects, such as flu-like symptoms, headache etc. which last for in the region of 24 hours. These usually disappear after a while. I judge the majority of patients experience no side-effects after a one year maximum. For me it took longer and I still draw from an occasional lower than the weather year.
You obligation to jump for regular check-ups and shouldn't pinch aspirins or drink hulking amounts of alcohol if you are on inteferon drug (it's complicated on the liver and blood-thinning.
MS is a markedly individual disease and one heaps culture (also those who enjoy no clue) enjoy an belief almost in relation to cures, treatments and the overall progression of your disease - which will usually be a intensely distrustful estimation, because they read this and hear that. Thing is that you regularly hear going on for the worst cases surrounded by the medium. IF you should be diagnosed near MS, afterwards don't frenzy, listen to your adjectives sense and your neurologist/doctor.