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Multiple
Sclerosis
What is Multiple Sclerosis?
 It is an Auto Immune Disease which is when the body
starts to destroy itself.
 It is a life-long disease with no cure.
 In MS, the body attacks and destroys the fatty tissue called
myelin that insulates an axon/nerve, and is called
demyelination.
 If damage is severe it can also destroy the nerve/axon itself.
 MS affects the central nervous system and inflames the
white matter in the brain which creates plaques. White matter
is below the top layer of our brain and spinal cord. Plaques
block a signal from being passed from the body to the spinal
cord and brain.
 Currently in the US, 250,000-300,000 people have been
diagnosed with MS and there are 200 new cases diagnosed
every week.
History of Multiple Sclerosis
 Multiple Sclerosis, also known as MS, was given its name,
multiple because of the numerous sites of demyelination and
  ‘sclerosis’ which means scarring. “There are accounts of
 probable MS dating back to the 14th century but the history
 of the disease really begins in the 19th century with the first
   illustrations and clear clinical description of the disease
beginning to appear in 1838” (Barnes 16). It was in Holland
on August 4, 1421, that the earliest descriptions were seen.
  Even though the previous description, the first actual case
  was first diagnosed in 1849. It was Jean-Martin Charcot
 who is credited with giving us the first signs and symptoms
                   of Multiple Sclerosis.
What Causes MS?
“Despite extensive research, we still don’t
 know what causes MS” (O'Connor 8).
  However they have found associations
 and links between many factors including
        genetic and environmental.
Genetic
Environmental
Sex                          Latitude
Racial Group                  SES
Family history               Migration
                              Infections
Genetic Factors
Sex:      Women are more likely to have MS than men by a 2:1
ratio. They also think that this is true because women are in
general more likely to have an Auto immune Disease.

Racial Group:               “Whites are more than twice as likely
as other races to develop MS” ( Hope 2).

Family History:                   In a normal population the chance
of someone to exhibit the symptoms of MS is only 0.1%. Now if
someone in your family has MS, the risk increases. If your parent,
brothers, or sisters (your first-degree relatives) have MS your
chance increases to 3%. If a second-degree relative has it, you
only have a 1% chance of having MS. If both of your parents have
the disease you have a risk of 20%. Other percentages are if you
have a half sister/brother, identical twin, or fraternal twin your
risks are as follows, 1.5%, 30%, and 3-4%.
***Remember that women have a slightly higher risk and that if
one identical twins has MS it is not 100% positive that the other
twin will have MS due to the environmental factors.
E nvironmental Factors
Latitude:              As you increase latitude, mainly above and below
40° latitude, MS is more common. These are temperate and cooler
climates. It is five times more likely in these regions.

SES:       Your socioeconomic status can also affect the occurrence of
MS. It is least common in the lower class and in rural residence.

Migration:                 The age at which you may move may also be an
important factor. “If you move before the age of 15, your risk is that of
the people in the country you move to. If you move after the age of 15,
your risk stays fixed at that of the country you grew up in” (O’Connor
15).

Infection:             “They believe MS is a delayed reaction to a viral
infection contracted during childhood by a genetically susceptible
person” (O’Connor 13). The viral infections may include shingles,
chicken pox, measles, or certain herpes. An idea they also have is the
age at which you get the infection. The older you are the higher the risk
for MS.
***Remember that in warm countries, children contract viruses at a
younger age.
What actually happens in the
                    Immune System?
  “T immune syst – acompl net or ofspeciaized cels a or ns – defends t bodya inst at cks by
     he           em          ex w k             l     l nd ga             he        ga ta
“for inv der such a ba er , v uses, fungi, a paa es” (Hope 3 Itgoes outl
     eign a s           s ct ia ir             nd r sit        ).            ooking fort inv der a
                                                                                       he a s nd
 kils t In ourbodyw ha e differ a igens, w ca a immune r
    l hem.               e v       ent nt        hich use n       esponse, fordiffer inv der W
                                                                                    ent a s. hen
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ofM T hel keep t immune syst in or a dir l destoyt infect orda ged cel. Howdo t
     S. hey p          he          em der nd ecty r he                ed      ma        l        hese
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  - l        ha he l hey r ta               n a ? el        ch         l her r r s ha et
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           em                 n l         eign            S ut                 se ha sons
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          he       ence w        f nd sel l not spect he                        em ha hey r ooking
                                           a is t bl br in
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 bar (bbb). T bbb is amembr ne t tsuround t br in a al s subst nces t cr fr t bl t t
    rier        he              a ha r he a nd low                  a o oss om he ood o he
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     rl v          em.           ha he          ea     nd      he             em           oss er nd
                                        ca da ge t t CNS.
                                           use ma o he
Diagnosing MS
• “The most important principle to consider when
  diagnosing MS is whether the person fulfils the diagnostic
  criteria on clinical grounds” (Barnes 29).
• To date there is no diagnostic or blood test for MS.
• Family physician will send you to a neurologist who goes
  over your symptoms and history.
• You can be given one of four test to help the doctor see if
  there is damage to the spinal cord and brain. These test are
  only half of the diagnostic process. The tests you can take
  are MRI, MRS, evoked potentials, and lumbar puncture.
• These tests may be able to rule out a viral infection that
  can exhibit the same symptoms as an MS attack.
• Remember that these tests are just as important as a
  clinical evaluation.
Diagnostic categories of MS
    •   “The phrase ‘multiple abnormalities in space and time’ sums up
        what a physician needs to find a diagnosis of MS” (O’Connor 32).
    •   There are three categories of MS; Definite, Probable, and Possible
        MS.
    •   Definite MS: “Consistent course (relapse-remitting course with at
        least 2 bouts separated by at least 1 month or slow or stepwise
        progressive course for at least 6 months) of documented
        neurological signs of lesions in more than one site of brain or spinal
        cord white matter” ( Hope 7). The age of onset is between 10 and
        50 years of age.
    •   Probable MS: Here the signs are not previously documented and
        there is one current sign of MS. There is more than one site of
        lesions, they have a good recovery and have a history of relapse-
        remitting symptoms.
    •    Possible MS: There is no documented signs of MS and more than
        one lesion. There is also a history of one relapse-remitting
        symptoms.
Courses of MS
Listed below are the different paths that MS can take.

• Relapse-remitting MS (RRMS): •      Secondary-progressive MS
   Here you have an attack, go        (SPMS): This stage of MS
  into complete or partial            starts with RRMS symptoms
  remission, then have the            and continues on to show signs
  symptoms return.                    of PPMS.
• Primary-progressive MS          •   Progressive-relapsing MS
  (PPMS): Here you continually        (PRMS): This is a rare form
  decline and have no remissions.     but here it takes a progressive
   There may be a temporary           route made worse by acute
  relief in symptoms.
                                      attacks.
• A few patients have malignant
  MS which is where they have a •     20% of the people with MS
  quick decline which leaves          have a benign form. Here they
  them severely disabled or even      show little progression after the
  lead to death.                      first attack.
Symptoms of MS
•   Fatigue                •   Weakness
•   Depression             •   Dizziness/Unsteadiness
•   Memory change          •   Numbness/Tingling
•   Pain                   •   Ataxia
•   Spasticity             •   Euphoria
•   Vertigo                •   Speech disturbance
•   Tremor                 •   Bladder/Bowel/Sexual
•   Double Vision/Vision       dysfunction
    Loss
Is disability inevitable?
 As mentioned above there are numerous
  different paths that MS can take you on.
“Although MS as a disease is much feared,
 the prognosis in general is not as poor as
      commonly thought” (Barnes 15).
 5-20% of all patients will develop benign
MS, and another 33% will have little to no
      disabilities allowing them to live
     independently while not in relapse.
   Only 33% of MS patients will have a
              severe disability.
Can I still have children?
   This question is important to many sufferers. This
   question is mainly for women though. It was once
  thought that women should not have children at all if
     she was diagnosed with MS. Actually during the
 mothers’ last trimester there is a 70% reduction in the
relapse rate. The thought behind this process is that the
mother’s immune system changes so her body does not
    reject the unborn child who has a different genetic
       makeup. Although there is a brief decrease in
 symptoms, within three months after the child is born,
 there is a similar increase in the relapse rate. Also, be
  aware of the medication and the effects it will have.
    Some drugs are not to be taken if you are going to
     become pregnant, are pregnant, or are nursing.
Medications used for MS
•   Spasticity- Baclofen, Tizanidine, Diazepam, Dantrolene
•   Optic Neuritis- Methlyprednisolone, Oral steroids
•   Fatigue- Antidepressant, Amantadine
•   Pain- Codeine, Aspirin
•   Sexual Dysfunction- Viagra, Pravatine
•   Tremor- Isoniazid, Primidone, Propranolol
•   Disease-Modifying Drugs- Interferon beta 1a and
    1b, and Glatiramer acetate
Disease-Modifying Drugs
• Interferon Beta 1a                  • Interferon Beta 1b
  (Avonex and Rebif):                   (Betaseron): is slightly
  is a protein that is a replica of     different from our own
  human interferon. It suppress         interferon. This medication
  the immune system and helps to        does the same thing as beta 1a,
  maintain the blood-brain              but is injected just under the
  barrier. You inject Avonex into       skin every two days. Side
  the muscle once a week and            effects include irritation,
  Rebif is injected under the skin      bruising, and redness at the site
  three times a week. This drug         of injection and the flu like
  is useful to people who have          symptoms. This is also given
  definite progressive MS. One          to people who have definite
  side effect of the drug is a flu      progressive MS.
  like symptom.
Disease-Modifying Drugs (con’t)
• Glatiramer Acetate ( Copaxone):                            “is a
       small fragment of a protein that resembles a protein in
     myelin” ( O’Connor 106). It decrease the reoccurrence of
     relapse. It is injected just under the skin every day. There
     is no flu like symptoms but occasional redness may occur
    at the injection site. A few amount of people do experience
                      brief shortness of breathe.

•    In summary all three of these drugs decrease relapses by
     33%, have manageable side effect, are injected, stabilize
              the disease, and tend to be costly.
At naiv Teament
                ler t e r t s
•   Acupuncture            • Homeotherapy
•   Aromatherapy           • Injection of Venom
•   Cannabis (Marijuana)     such as snake and bee
•   Chiropractic           • Massage
•   Cold Immersion         • Meditation
•   Dietary Supplements    • Reflexology
•   Herbal Medication      • Tai Chi
                           • Yoga

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madicine.Multiplesclerosis.(dr.muhamad tahir)

  • 2. What is Multiple Sclerosis?  It is an Auto Immune Disease which is when the body starts to destroy itself.  It is a life-long disease with no cure.  In MS, the body attacks and destroys the fatty tissue called myelin that insulates an axon/nerve, and is called demyelination.  If damage is severe it can also destroy the nerve/axon itself.  MS affects the central nervous system and inflames the white matter in the brain which creates plaques. White matter is below the top layer of our brain and spinal cord. Plaques block a signal from being passed from the body to the spinal cord and brain.  Currently in the US, 250,000-300,000 people have been diagnosed with MS and there are 200 new cases diagnosed every week.
  • 3. History of Multiple Sclerosis Multiple Sclerosis, also known as MS, was given its name, multiple because of the numerous sites of demyelination and ‘sclerosis’ which means scarring. “There are accounts of probable MS dating back to the 14th century but the history of the disease really begins in the 19th century with the first illustrations and clear clinical description of the disease beginning to appear in 1838” (Barnes 16). It was in Holland on August 4, 1421, that the earliest descriptions were seen. Even though the previous description, the first actual case was first diagnosed in 1849. It was Jean-Martin Charcot who is credited with giving us the first signs and symptoms of Multiple Sclerosis.
  • 4. What Causes MS? “Despite extensive research, we still don’t know what causes MS” (O'Connor 8). However they have found associations and links between many factors including genetic and environmental. Genetic Environmental Sex Latitude Racial Group SES Family history Migration Infections
  • 5. Genetic Factors Sex: Women are more likely to have MS than men by a 2:1 ratio. They also think that this is true because women are in general more likely to have an Auto immune Disease. Racial Group: “Whites are more than twice as likely as other races to develop MS” ( Hope 2). Family History: In a normal population the chance of someone to exhibit the symptoms of MS is only 0.1%. Now if someone in your family has MS, the risk increases. If your parent, brothers, or sisters (your first-degree relatives) have MS your chance increases to 3%. If a second-degree relative has it, you only have a 1% chance of having MS. If both of your parents have the disease you have a risk of 20%. Other percentages are if you have a half sister/brother, identical twin, or fraternal twin your risks are as follows, 1.5%, 30%, and 3-4%. ***Remember that women have a slightly higher risk and that if one identical twins has MS it is not 100% positive that the other twin will have MS due to the environmental factors.
  • 6. E nvironmental Factors Latitude: As you increase latitude, mainly above and below 40° latitude, MS is more common. These are temperate and cooler climates. It is five times more likely in these regions. SES: Your socioeconomic status can also affect the occurrence of MS. It is least common in the lower class and in rural residence. Migration: The age at which you may move may also be an important factor. “If you move before the age of 15, your risk is that of the people in the country you move to. If you move after the age of 15, your risk stays fixed at that of the country you grew up in” (O’Connor 15). Infection: “They believe MS is a delayed reaction to a viral infection contracted during childhood by a genetically susceptible person” (O’Connor 13). The viral infections may include shingles, chicken pox, measles, or certain herpes. An idea they also have is the age at which you get the infection. The older you are the higher the risk for MS. ***Remember that in warm countries, children contract viruses at a younger age.
  • 7. What actually happens in the Immune System? “T immune syst – acompl net or ofspeciaized cels a or ns – defends t bodya inst at cks by he em ex w k l l nd ga he ga ta “for inv der such a ba er , v uses, fungi, a paa es” (Hope 3 Itgoes outl eign a s s ct ia ir nd r sit ). ooking fort inv der a he a s nd kils t In ourbodyw ha e differ a igens, w ca a immune r l hem. e v ent nt hich use n esponse, fordiffer inv der W ent a s. hen t r inv dera a igen met t a igen mulipl t destoyt inv der Tcels ae aso impora in t r e he ight a nd nt , he nt t es o r he a . - l r l t nt he ol ofM T hel keep t immune syst in or a dir l destoyt infect orda ged cel. Howdo t S. hey p he em der nd ecty r he ed ma l hese Tcels knowt tt cel t ae at cking is a inv der W lon ea ofourcels t e ae maker t tl our - l ha he l hey r ta n a ? el ch l her r r s ha et immune syst knowitis ourow cel orafor body. Since M is aa oimmune disea t tper bodydoes em n l eign S ut se ha sons notknowt differ bet een sel a non- fcels. A hera oft immune syst t tt ae l he ence w f nd sel l not spect he em ha hey r ooking a is t bl br in t he ood- a bar (bbb). T bbb is amembr ne t tsuround t br in a al s subst nces t cr fr t bl t t rier he a ha r he a nd low a o oss om he ood o he cent a ner ous syst Some feelt tt bbb is br ched a some oft immune syst defense cr ov a rl v em. ha he ea nd he em oss er nd ca da ge t t CNS. use ma o he
  • 8. Diagnosing MS • “The most important principle to consider when diagnosing MS is whether the person fulfils the diagnostic criteria on clinical grounds” (Barnes 29). • To date there is no diagnostic or blood test for MS. • Family physician will send you to a neurologist who goes over your symptoms and history. • You can be given one of four test to help the doctor see if there is damage to the spinal cord and brain. These test are only half of the diagnostic process. The tests you can take are MRI, MRS, evoked potentials, and lumbar puncture. • These tests may be able to rule out a viral infection that can exhibit the same symptoms as an MS attack. • Remember that these tests are just as important as a clinical evaluation.
  • 9. Diagnostic categories of MS • “The phrase ‘multiple abnormalities in space and time’ sums up what a physician needs to find a diagnosis of MS” (O’Connor 32). • There are three categories of MS; Definite, Probable, and Possible MS. • Definite MS: “Consistent course (relapse-remitting course with at least 2 bouts separated by at least 1 month or slow or stepwise progressive course for at least 6 months) of documented neurological signs of lesions in more than one site of brain or spinal cord white matter” ( Hope 7). The age of onset is between 10 and 50 years of age. • Probable MS: Here the signs are not previously documented and there is one current sign of MS. There is more than one site of lesions, they have a good recovery and have a history of relapse- remitting symptoms. • Possible MS: There is no documented signs of MS and more than one lesion. There is also a history of one relapse-remitting symptoms.
  • 10. Courses of MS Listed below are the different paths that MS can take. • Relapse-remitting MS (RRMS): • Secondary-progressive MS Here you have an attack, go (SPMS): This stage of MS into complete or partial starts with RRMS symptoms remission, then have the and continues on to show signs symptoms return. of PPMS. • Primary-progressive MS • Progressive-relapsing MS (PPMS): Here you continually (PRMS): This is a rare form decline and have no remissions. but here it takes a progressive There may be a temporary route made worse by acute relief in symptoms. attacks. • A few patients have malignant MS which is where they have a • 20% of the people with MS quick decline which leaves have a benign form. Here they them severely disabled or even show little progression after the lead to death. first attack.
  • 11. Symptoms of MS • Fatigue • Weakness • Depression • Dizziness/Unsteadiness • Memory change • Numbness/Tingling • Pain • Ataxia • Spasticity • Euphoria • Vertigo • Speech disturbance • Tremor • Bladder/Bowel/Sexual • Double Vision/Vision dysfunction Loss
  • 12. Is disability inevitable? As mentioned above there are numerous different paths that MS can take you on. “Although MS as a disease is much feared, the prognosis in general is not as poor as commonly thought” (Barnes 15). 5-20% of all patients will develop benign MS, and another 33% will have little to no disabilities allowing them to live independently while not in relapse. Only 33% of MS patients will have a severe disability.
  • 13. Can I still have children? This question is important to many sufferers. This question is mainly for women though. It was once thought that women should not have children at all if she was diagnosed with MS. Actually during the mothers’ last trimester there is a 70% reduction in the relapse rate. The thought behind this process is that the mother’s immune system changes so her body does not reject the unborn child who has a different genetic makeup. Although there is a brief decrease in symptoms, within three months after the child is born, there is a similar increase in the relapse rate. Also, be aware of the medication and the effects it will have. Some drugs are not to be taken if you are going to become pregnant, are pregnant, or are nursing.
  • 14. Medications used for MS • Spasticity- Baclofen, Tizanidine, Diazepam, Dantrolene • Optic Neuritis- Methlyprednisolone, Oral steroids • Fatigue- Antidepressant, Amantadine • Pain- Codeine, Aspirin • Sexual Dysfunction- Viagra, Pravatine • Tremor- Isoniazid, Primidone, Propranolol • Disease-Modifying Drugs- Interferon beta 1a and 1b, and Glatiramer acetate
  • 15. Disease-Modifying Drugs • Interferon Beta 1a • Interferon Beta 1b (Avonex and Rebif): (Betaseron): is slightly is a protein that is a replica of different from our own human interferon. It suppress interferon. This medication the immune system and helps to does the same thing as beta 1a, maintain the blood-brain but is injected just under the barrier. You inject Avonex into skin every two days. Side the muscle once a week and effects include irritation, Rebif is injected under the skin bruising, and redness at the site three times a week. This drug of injection and the flu like is useful to people who have symptoms. This is also given definite progressive MS. One to people who have definite side effect of the drug is a flu progressive MS. like symptom.
  • 16. Disease-Modifying Drugs (con’t) • Glatiramer Acetate ( Copaxone): “is a small fragment of a protein that resembles a protein in myelin” ( O’Connor 106). It decrease the reoccurrence of relapse. It is injected just under the skin every day. There is no flu like symptoms but occasional redness may occur at the injection site. A few amount of people do experience brief shortness of breathe. • In summary all three of these drugs decrease relapses by 33%, have manageable side effect, are injected, stabilize the disease, and tend to be costly.
  • 17. At naiv Teament ler t e r t s • Acupuncture • Homeotherapy • Aromatherapy • Injection of Venom • Cannabis (Marijuana) such as snake and bee • Chiropractic • Massage • Cold Immersion • Meditation • Dietary Supplements • Reflexology • Herbal Medication • Tai Chi • Yoga