Tysabri outreach unified commitment
Common Questions and Answers about Tysabri outreach unified commitment
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When I agreed to live together I was already certain that I wanted to marry him, but no commitment of that sort has ever come from his side. I have mentioned the subject at several occasions, I have hinted and I have even accused him of not wanting to commit, but he just sticks to the excuse that he cannot marry me if he is not in a financial position to support me.
3 months ago we bought our house which i put the deposit down for. I know we have made a big commitment buying a house together, but my partner will not discuss our future, i have tried to mention it a few times. I have now given up, he will just say who is getting married or who is having children! His family are going on at him about marriage and children but he just ignores their comments and conversations. Im wondering why he agreed to a mortgage if he isnt sure what he wants?
Sounds "commitment phobe-ish" to me.
Dear Carmenmiranda,
The term commitment-phobic is convenient, but doesn’t tell us much beyond what we already know, that your boyfriend is betwixt and between, ambivalent as anything, all over the place. Yes he’s phobic about making a long-term relationship, but why? My best guess from pondering your email, is that he’s right about there being something missing. However, my other guess is that what’s missing is in him, not you or the relationship per se.
They found out the reason people contracted PML was because they were taking Avonex/and the other MS medications with Tysabri. I think the Tysabri has given me a second chance at helping slow my disease progress, but with out it I would be on no MS medications to slow the disease. I did alot of research before I decided to start the medication and the one resource that helped me make my decision was reading the Tysabri diaries on line.
www.msrc.co.uk/index.cfm?
I have had MD for 18 years. Been on Avonex, Betaseron, Tysabri, and now Tecfidera. Unfortunately, I'm also on lots of other medications, mostly due to terrible central pain. My neurologist made me stop the Tysabri after 24 infusions because of safety concerns. I felt my overall best while on Tysabri and have asked him if and when I might be able to go back on the monthly infusions. He does not have an answer for me at this point.
Are any of you on Tysabri? My doctor has suggested that I consider starting Tysabri treatment. His neurology practice runs a TOUCH infusion center. I've been on Copaxone for four years and have just had my first flareup. My recent MRI shows progression of MS with T2 hyperintense white matter lesions in the pons of the brainstem and the frontal lobe. Several of the older lesions have increased in size. Five years ago I was on Avonex. I had multiple flare-ups the whole year on this med.
I would like some information/details from anyone who has had (or seen) the rash you can get from Tysabril and/or PML?? I have been on Tysabri 10 years so far without any major issues. I was outside after my treatment for 10 minutes or so. After taking my shirt off, my husband gasped and asked what was wrong with my back.
I think they are lacking in leadership because they don’t seem to be unified in what they are standing for or fighting against. This makes them look like nothing more than a group of contentious, complaining, whiners. It is going to be interesting to see what happens from here, will it grow or will it fizzle out? Nature itself teaches us that anything that doesn’t grow will die.
So now he wants to take me off of the Copaxone, I have been on for a month and a half, and put me on Tysabri. I started the application process and now waiting for them to call me and get the ball rolling on that. Now he mentioned that this is the top of the line MS medication so that does give me some relief.
P.S. I did test negetive for the JC Virus.
Any thoughts, experiences etc on this Tysabri??!!
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