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#1 | ||
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Junior Member
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How has the Tecfifera worked for you?
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#2 | |||
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Member
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I will say Tecfidera is a great drug & excellent form compared to shots.
Side effects were nill after a month or so & Tecfidera surely works. I wanted Tysabri back. My MS progresses on either but Ty has the edge. If I has to pick between any of the injectables or a pill twice/day, i'd surely try the pill IF, shots weren't holding me/you steady. For travelers, a pill's hard to beat. |
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#3 | ||
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Junior Member
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Well my meds are due here tomorrow and as much as I am happy I don't have to do shots every day, I am a little nervous about the tec, but staying positive. I'm just a bit confused about the aspirin and antacids I have to take with it. Can someone tell me what has worked best for them? What brand of antacid of aspirin?
Thank you! |
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#4 | ||
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Junior Member
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Hi everyone,
I was Dx 6/2004. My Dr put me on Avonex, after 6-8 months he changed me to Rebif because I am a major needle phobe! I used Rebif for about 4-5 years and had to discontinue because of needle site reactions. He put me back on Avonex and I have used it until about 1 1/2 months ago. I finally hit a major level of needle fatigue. My current doc prescribed Tecfidera and I started on it on Feb. 23. The 1st week and a half were very uneventful, maybe a but of flushing. The last few days I am having quite a bit of stomach cramping and mild headaches. I also have noticed more fatigue than is typical for me, but I am also dealing with a number of stressors! I plan to battle through it until the dr orders blood work. As long as that comes back ok I plan to stay on this path. |
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"Thanks for this!" says: | ewizabeth (08-28-2014) |
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#5 | |||
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Member
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called Ms active source today and they have my application for the BG12! Said they received it April 20. They told me to wait for the pharmacy to call!
__________________
. If you obsess about things that may happen and they don't come true...then you've wasted your time. If it does come true....then you've lived it twice. . |
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"Thanks for this!" says: | ANNagain (05-06-2013) |
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#6 | |||
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Senior Member
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Just called, and again, they don't have my application. Tomorrow I'll make sure my neuro's nurse has the right fax number. It won't be such a new med by the time I get it.
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RRMS, diagnosed '00 Everything will be alright in the end. If it's not alright, it's not yet the end. |
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#7 | |||
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Member
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Good news!! I pick-up starting dose 120mg 2x/day for 1 week tomorrow!!!
Next week I get the full 240mg 2x/day dose!! Hurray!! Do I look forward to flushing, pooping, and possible headaches? No, but ..Hurray!!! |
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"Thanks for this!" says: | SallyC (05-13-2013) |
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#8 | |||
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Member
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Started the 120mg twice a day for 1st week dose last night & no side effects at all..yet! Just tell yourself no problem and think of bright side.
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#9 | |||
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Member
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Just finishing my 2nd week. So far a little flushing and headaches. When I take ibuprofen or aspirin at the same time no headache. Neuro appt. next month will try to get ampyra and see if that will lessen impact of ms. Reaction better than what I had with rebif. Pop the pill and go. Flushing could be heat related, 90 degrees yesterday.
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#10 | ||
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New Member
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