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01-23-2011, 03:42 PM | #21 | ||
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I am new to Tysabri, and should be starting my infusions real soon. My question is....How do I know if I am a part of the stratify II study? Do you sign up or are you asked to join?
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01-24-2011, 03:21 PM | #22 | ||
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If you received a JC Virus antibody test, you are in strafiy II study as the test is only available in the study.
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01-24-2011, 08:34 PM | #23 | ||
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I just heard from the Tysabri assistance program, and I qualified for a $10.00 co-pay for the Tysabri. But they told me there is a second fee for the infusion site that Biogen does not/can not help with. According to my insurance company that is an additional $40.00 co-pay.
I should begin my infusions real soon now. Just curious....what do you all pay for your infusions? I am sure I am getting a good deal, however, I am not sure where I will get an extra $50.00 a month from....yes, it is really that tight financially in our home. Still have three kids at home too. |
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01-25-2011, 06:16 PM | #24 | |||
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The cost of my medication went up a year ago. Now I pay $125 for the medication plus a $35 co-pay for a doctor's visit to get the infusion. At $160 an infusion I still consider that a steal compared to some other stories I have heard about costs. And I have a major insurance company PPO plan with a company that has thousands of employees.
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On Tysabri and love it. . |
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01-26-2011, 01:01 PM | #25 | |||
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Magnate
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I'm no help with insurance costs. I have a full service plan from the old days that pays all my hospital costs, and my infusion is done in an oncology center at a local hospital. I have no copay.
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I know the sound the river makes, by dawn, by night, by day. But can it stay me through tomorrows that find me far away? . I have this mental picture in my mind of you all, shaking bones and bells and charms, muttering prayers and voodoo curses, dancing around in a circle of salt, with leetle glasses and tiny bottles of cheer in the middle...myyyyyy friends! diagnosed 09/03/2004 scheduled to start Tysabri 03/05 Tysabri withdrawn from market 02/28/05 Copaxone 05/05-12/06 Tysabri returned to market 06/05/06 Found a new neuro 04/07 Tysabri 05/25/07-present Medical Marijuana legally 12/03/09 . Negative for JC virus antibodies! . I'm doing alright and making good grades, The future's so bright, I gotta wear shades! . |
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01-26-2011, 01:53 PM | #26 | ||
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I am on Medicare and have a federal plan (husband was a federal firefighter) for my secondary. I do not have a copay- I am very fortunate for the healthcare my husband and I have.
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01-26-2011, 08:52 PM | #27 | |||
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can anyone clue me in to side effects? i had my 1st infusion on Jan 14th and on the 24th i started to feel sick, like a chest cold. if this is from the tysabri will it go away like a regular cold ? i'm also very fatigued. my headaches have stopped though
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Multiple Sclerosis Diagnosed August 2010 |
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01-27-2011, 09:34 AM | #28 | |||
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Magnate
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Side effects: I think each body is different. For me, I get a sinus infection and a uti that both hit around the same time, 3-5 days after the infusion. The day of infusion I usually get really tired, and just drained of energy and that lasts about 2 days.
I also have really bad joint pain but I don't know that I can blame that on the ty seeing as I was having that issue long before I stared it. But on the plus side, my last 2 MRIs have shown no new lesions. Some people feel great with it and can tell when they are getting close to their infusion. Personally, it hasn't happened for me. Good luck though. Glad to hear the headaches are gone. I know that is a relief.
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. I am not spoiled! |
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01-27-2011, 12:37 PM | #29 | ||
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Quote:
I was sooo fatigued one day I almost couldn't move off the chair. I was scared that my ms symptoms has worsened The next day I was much better and today I am back to normal !!! Glad your headaches have stopped, hope you feel better soon and that Ty works great for you Linda |
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01-27-2011, 02:57 PM | #30 | ||
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I am scheduled to get my first infusion on Feb 2. We are leaving on vacation on Feb 10th.
I realize that everyones reactions are different, but, if you do get side effects, do they last more than a week? I am hoping I will feel okay on the day we are to leave. thanks |
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