Guest guest Posted September 10, 2010 Report Share Posted September 10, 2010 Well, being off therapy since May is killing me!!!! My neuro has decided to put me on Copaxone until "the pill" comes out. Funny, "the pill" always had a different meaning to us ladies didn't it? So, all you fellow MSers need to fill me in on this drug! I've done the Rebif, Avonex and Tysabri. They all quit working so I've got to get on something to thwart some of these symptoms until "the pill" is approved by our glorious FDA for use in the good ole USA. Been having some lovely numb spots everywhere! The other day I swear I woke up to an epidural, but only in my back. Now that was a nice feeling for a change! Usual I ache so bad from the fibro in my lower back that I actually welcomed that nice MS symptom. But the numbness and tingling and sometimes almost paralizing symptoms have gotten to be too much so Copaxone here we come! Tammy, Tx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 10, 2010 Report Share Posted September 10, 2010 Tammy I am sorry you are having a rough time. You are in my prayers. Hugs nne To the world you might be one person, but to one person you just might be the world""May the Lord Bless you and keep you,May the Lord Make his face shine upon you, and give you Peace...Forever"Breast Cancer Patients Soul Mates for Lifehttp://breastcancerpatientssoulmatesforlife.bravehost.com/ Anxiety Depression and Breast Cancerhttp://health.groups.yahoo.com/group/AnxietyDepressionandBreastCancerAngel Feather Loomerwww.angelfeatherloomer.blogspot.comThe Cancer Clubwww.cancerclub.com -----Original Message-----From: tamatha_tx@...Sent: Fri, 10 Sep 2010 06:20:58 -0700 (PDT)To: mserslife Subject: Copaxone-I'm starting Well, being off therapy since May is killing me!!!! My neuro has decided to put me on Copaxone until "the pill" comes out. Funny, "the pill" always had a different meaning to us ladies didn't it? So, all you fellow MSers need to fill me in on this drug! I've done the Rebif, Avonex and Tysabri. They all quit working so I've got to get on something to thwart some of these symptoms until "the pill" is approved by our glorious FDA for use in the good ole USA. Been having some lovely numb spots everywhere! The other day I swear I woke up to an epidural, but only in my back. Now that was a nice feeling for a change! Usual I ache so bad from the fibro in my lower back that I actually welcomed that nice MS symptom. But the numbness and tingling and sometimes almost paralizing symptoms have gotten to be too much so Copaxone here we come! Tammy, Tx Free 3D Earth Screensaver Watch the Earth right on your desktop! Check it out at www.inbox.com/earth Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 10, 2010 Report Share Posted September 10, 2010 Hi Tammy, I hope it works for you. Take care of yourself. Love Margaret >Well, being off therapy since May is killing me!!!! My neuro has decided to put me on Copaxone until " the pill " comes out. Funny, " the pill " always had a different meaning to us ladies didn't it? So, all you fellow MSers need to fill me in on this drug! I've done the Rebif, Avonex and Tysabri. They all quit working so I've got to get on something to thwart some of these symptoms until " the pill " is approved by our glorious FDA for use in the good ole USA. Been having some lovely numb spots everywhere! The other day I swear I woke up to an epidural, but only in my back. Now that was a nice feeling for a change! Usual I ache so bad from the fibro in my lower back that I actually welcomed that nice MS symptom. But the numbness and tingling and sometimes almost paralizing symptoms have gotten to be too much so Copaxone here we come! > >Tammy, Tx > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 10, 2010 Report Share Posted September 10, 2010 Dears TammyI'm sorry to hear of your current/continuing problems. I sure hope the Copaxone works for you!big hugs SharonThis email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: mserslife <MSersLife >Sent: Fri, September 10, 2010 6:20:58 AMSubject: Copaxone-I'm starting Well, being off therapy since May is killing me!!!! My neuro has decided to put me on Copaxone until "the pill" comes out. Funny, "the pill" always had a different meaning to us ladies didn't it? So, all you fellow MSers need to fill me in on this drug! I've done the Rebif, Avonex and Tysabri. They all quit working so I've got to get on something to thwart some of these symptoms until "the pill" is approved by our glorious FDA for use in the good ole USA. Been having some lovely numb spots everywhere! The other day I swear I woke up to an epidural, but only in my back. Now that was a nice feeling for a change! Usual I ache so bad from the fibro in my lower back that I actually welcomed that nice MS symptom. But the numbness and tingling and sometimes almost paralizing symptoms have gotten to be too much so Copaxone here we come! Tammy, Tx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2010 Report Share Posted September 11, 2010 Hi Tammy,I too was on tysabri, and now I'm back on Copaxone. I amstable, and my MRI did not show any worsening of lesions.If you have any further questions,let me know; I'd be happyto answer any.hugs, Kate Copaxone-I'm startingTo: mserslife > Well, being off therapy since May is killing me!!!! My neuro > has decided to put me on Copaxone until "the pill" comes out. > Funny, "the pill" always had a different meaning to us ladies > didn't it? So, all you fellow MSers need to fill me in on this > drug! I've done the Rebif, Avonex and Tysabri. They all quit > working so I've got to get on something to thwart some of these > symptoms until "the pill" is approved by our glorious FDA for > use in the good ole USA. Been having some lovely numb spots > everywhere! The other day I swear I woke up to an epidural, but > only in my back. Now that was a nice feeling for a change! > Usual I ache so bad from the fibro in my lower back that I > actually welcomed that nice MS symptom. But the numbness and > tingling and sometimes almost paralizing symptoms have gotten to > be too much so Copaxone here we come!> > Tammy, Tx> > > love and blessings,Kate Attachment: vcard [not shown] Quote Link to comment Share on other sites More sharing options...
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