Patients Helping Patients®
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| General Questions and Answers For learning, sharing your experience, and exchanging information about Multiple Sclerosis. Please discuss medications in the Medications forum, and natural supplements in Tara's forum. |
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#16
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Dx at 27, 36 now.
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#17
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DX at age 57, history of overlooked symptoms reaching back ~35 years.
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#18
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First sx near 50, dx of RRMS at 58. Drop foot and later, a weak hand, both right side. Now 62... Male BTW.
Have to say my MS doesn't seem very remitting.... Jer |
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#19
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I was DX'ed at 30 but in hindsight my first symptoms were showing a year earlier. I'm 39 now...
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" An eye for an eye; and soon the whole world is blind" -- Mahatma Ghandi |
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#20
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age 49
first symptom age 49, dx. age 49 progressive ms. in 4 years went from only a hand tremor and dropfoot to wheelchair.
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"Be kinder than necessary because everyone you meet is fighting some kind of battle" |
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#21
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ANOTHER REASON TO HATE THIS DAY
DX'D APRIL 15, 2002.
i'd turned 40 in january. during my 30th year i was dxd and treated for Lyme Disease in 3rd stage (brain) i turned 50 in jan. don't want to be superstitious, but wondering what this yr will bring. unfortunately there are some things worse than MS. and I DONT WANT THEM! ![]() back to dx, he back dated it at least 10 yrs if not more. probably my 2nd pregnancy at 27 is what he thought, either that or the lyme flipped the MS switch. of course, they don't know for sure i pray that all are managing well. that first dx really threw me, but the Lord brought me through it without all the bitterness that was trying to creep in. take care and God bless ya! ![]()
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"Nothing is impossible., the word itself says I'm possible" Audrey Hepburn |
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#22
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47 when diagnosed, but can remember symptoms from in my 30'sl
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Sue Previous Meds: Avonex, Copaxone Beta Babe: January 2007 |
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#23
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For me 36 and I'm still 36 so I guess I am a noob lol
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Ankylosing Spondylitis DX- Sept 2008, MS DX- November 2011,RRMS- 1-11-12, Copaxone -3-2-12 |
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#24
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AGE 53
Finally found out had PPMS at age 53 but had symptoms for 2 yrs before. Am in power wheelchair now. Can't walk.
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#25
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Hi everyone,
I guess I am the oldest so far: Never have a problem and at 62 from no where was DX RRMS with my first attack!! Ms hug, fatigue, dizziness, vertigo and all the good staff. I am now 65, on Copaxone and stable. I try to stay healthy as best I can, mostly vegetarian, yoga and now ride my bike. Good luck to you all. Alain |
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#26
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I'll add my age to this old group: 45 at diagnosis, 42 first bout of ON. Earlier symptoms? It's either 42 or 30, but there are many causes of the symptom I had - no numbness or tingling until after 42.
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#27
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49 and 11 months. 1 relapse and 1 new symptom after about 4 years.
Undxed last fall. 62 now techie
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Another pirated saying: Half of life is if. When today is bad, tomorrow is generally a better day. Dogs Rule!
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#28
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My first flare was at age 43 2008
Diagnosed at age 45 Age now 47 |
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#29
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Dx age 48, although told probably MS age 42.
Twenty years ago I lost my sense of smell. Ten weeks later it was replaced with the most offensive smell and taste. Everything in the world smelt and tasted just as disgusting. Three years later my normal smell/taste slowly came back. I still wonder today if that was a sign of MS. |
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#30
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First symptoms..... I have been tired since age 15 in '85. Blurred vision and Tingling on Right side began at age 35. Headaches followed shortly. Fast forward to age 42. A flare like a scud bomb.
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Sx: 12/30/11. Dx: 2/3/12. 6-8 lesions medulla/cervical spine. Copaxone 3/12. Trileptal 100 mg 4x/day Amantadine 300 mg, Baclofen 1/2 pill 4x/day. |
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