copaxone new zealand

It’s why I had such a love affair with copaxone. Most natural. Latest mri had shown 4 new lesions/ mild progression. But noted overall disease burden is mild. I guess the argument is my doc wants to keep it that way. Any thoughts? Ty!! Andrea.

Any other new zealand mummies to be out there? Im 24 and 18/4 due 7th June with my first. Just wondering if anyone else is from NZ as ive only been living here a few months and maternity care is all totally different from the UK.

we hate changes, don't we? Will you call them about the new Copaxone dosing? Going to that 3 times a week may be more confusing with this lack of diagrams but I know you can handle it!

Hi, my names Demelza, I am 37 and live in New Zealand. I am a stay at home mum with 4 awesome kids aged 4,6,8,10. I came here as I have just had my third MRI in a year and I am still very confused. Public funding of MS drugs is limited to older ones and you must met strong criteria to get them. Our public health system has very little user pays in it. So hi.

Is there anyone in new zealand on this site. If so I have started a page on facebook for you to come and join if you would like. I am looking for people in new zealand as I am the only one that I know of. There are also other sites for other places like america and australia. All you need to do is join facebook and then search for New Zealand Chiari or if you are from else where just put where you are from then chiari. These are support groups as well and you can share your story.

just want to know how safe would be my partner if we get married? we are planning to get married in new zealand because my bf is in new zealand..is it also possible that nz immigration granted my finace visa though i am hepa b carrier?

Sorry about my English , I am from New Zealand , 33years old male, recived unprotect oral sex from sex worker on 10/07/14 has been 17days am so worry about syhilis hiv ect especially I fond out coupe red spot on my balanus yesterday ,had std test at 14 days every thing was fine I know a bit early however really scare about syhilis hpv and hiv please help only had oral sex no others

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Hi! I just moved to new Zealand, and dont know what to do about my contraception, I usually took pills but I'm running out of them and don't really know what to do or take here. Going to a doctor is going to be really expensive now, so I was thinking to start using the BASAL Thermomether system? Does anybody know something about it??

Since then when I wash my hands I have this burning sensation when the water hits them. Has anyone else experienced this? Is it the copaxone or just a new symptom/flare with the ms? Thanks in advance for the comments!

Hi Trude! Glad to see you made it home ok! Did you enjoy the rest of your holiday? We sure enjoyed meeting you and I hope that we can be of some help here for you! I am going to send a message to Monotreme...that is whose hubby was just diagnosed with PPMS and ask her to send you a message about the Copaxone he is taking. She may be able to help you out somewhat and at the very least you can swap notes on what is going on ok?

What is the best way to get help paying for copaxone or is there a generic version that is less expensive? I was hoping to start taking it soon, but Im afraid I can't afford it. Also, has anyone taken the new oral version? Is it less expensive? I was advised not to use it but I certainly will if I can afford it. Plus, what are the other benefits of using copaxone othr than slowing down the formation of new lesions. Will I get my energy back? Will my concentration get better?

I am new to the website, and new to Capaxone. My question is what side effects does any one have to this stuff. Injection site is to be expected but the general body feeling. It is driving me nuts. I appreciate any remarks and comments.

Copaxone new zealand

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