This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.

Register

FAQ

It is currently Tue May 21, 2013 3:27 am

View unanswered posts | View active topics

Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

All times are UTC - 8 hours [ DST ]

Revimmune (cyclophosphamide or cytoxan)

Post new topic

Page 2 of 5

[ 213 topics ]

Go to page Previous 1, 2, 3, 4, 5 Next

Topics

Author

Replies

Views

Last post

white count 6600!!

5

2273

Mon May 25, 2009 5:33 am

Nine Weeks Post Treatment-NC

1

1790

Fri May 22, 2009 8:20 am

white count 730 and rising

2

1543

Thu May 21, 2009 11:12 am

white count 110 and dropping...

1

1551

Sun May 17, 2009 1:08 pm

IPOP/HIPOP Post-chemo update

2

1713

Fri May 15, 2009 11:39 am

Ginger eases chemotherapy nausea

0

1331

Fri May 15, 2009 4:28 am

Days 3 & 4 - chemo done!

3

1853

Thu May 14, 2009 9:34 am

More therapies for MS disease

0

1613

Sun May 10, 2009 9:53 am

Day 2

2

1402

Sun May 10, 2009 6:15 am

Baltimore in May?

[ Go to page: 1, 2 ]

26

4804

Sat May 09, 2009 7:54 am

Depression from Copaxone

2

1529

Fri May 08, 2009 12:38 pm

Day 1

6

1782

Fri May 08, 2009 12:29 pm

Copaxone free

8

2088

Fri May 01, 2009 8:34 am

PT Schedule

13

2527

Tue Apr 28, 2009 11:19 am

Heres something interesting for you

[ Go to page: 1, 2 ]

18

3619

Tue Apr 28, 2009 8:33 am

I did High Dose Cytoxan Treatment in North Carolina.

[ Go to page: 1, 2 ]

16

4610

Wed Apr 08, 2009 10:12 am

To re-dose or not...?

2

1605

Tue Apr 07, 2009 7:36 am

Almost 12 months on from HiCy - MRI Results and Round Up

[ Go to page: 1, 2 ]

16

3445

Tue Apr 07, 2009 7:31 am

MRI comparison shots

2

1458

Sat Apr 04, 2009 3:09 pm

Getting an MRI monday

Guest

1

921

Tue Mar 31, 2009 5:19 pm

MBP8298 vs Copaxone

10

3083

Thu Mar 26, 2009 10:39 am

Letter from Baxtor

3

1464

Wed Mar 25, 2009 5:37 pm

Newbie Question

9

1939

Mon Mar 23, 2009 12:22 pm

Contact info

Guest

4

1236

Sat Mar 14, 2009 7:22 am

Finally the cat is out of the bag

0

1461

Fri Mar 13, 2009 9:15 am

Vitamin D levels

[ Go to page: 1, 2 ]

17

3146

Wed Mar 11, 2009 11:11 am

Re-dosing

7

1616

Wed Mar 11, 2009 10:20 am

*FINALLY!!* - I have my new appointment dates.

[ Go to page: 1, 2 ]

23

3531

Sun Mar 08, 2009 5:00 pm

What phase of testing is revimmue in?

Guest

13

1704

Sat Mar 07, 2009 5:19 pm

Ok...I picked my hotel....

3

1548

Sat Mar 07, 2009 5:18 pm

Notes from my HiCy experience...

11

3009

Thu Mar 05, 2009 10:03 pm

re-dosing

0

1046

Wed Mar 04, 2009 10:57 pm

Another exacerbation

4

1565

Mon Mar 02, 2009 9:54 am

Keri whats up??

4

1438

Mon Mar 02, 2009 9:24 am

MRI results

3

1191

Fri Feb 27, 2009 8:22 am

Progress...possibly.

2

1329

Tue Feb 24, 2009 9:12 am

my follow-up appt...

9

1687

Tue Feb 17, 2009 6:20 pm

JH Continues to Blow Me Off...

0

1327

Sat Feb 14, 2009 5:36 pm

Here goes 'nuthin

4

1355

Fri Feb 13, 2009 3:34 pm

Second doses?

1

1174

Sat Feb 07, 2009 10:04 am

My MRI Results

9

1565

Sat Feb 07, 2009 4:44 am

JH's Clinical trial

3

1307

Thu Feb 05, 2009 2:02 pm

So Keri and Me?

[ Go to page: 1, 2 ]

20

3218

Thu Feb 05, 2009 6:54 am

To a new year...how is everyone?

9

2032

Sun Jan 18, 2009 11:24 am

Jobs??

4

1642

Fri Jan 16, 2009 4:23 pm

symptoms while recovering from HiCy?

1

1359

Mon Dec 29, 2008 5:27 pm

Copaxone \ HiCy Reasearch

7

2221

Mon Dec 29, 2008 4:32 pm

Original HiCyers

6

2143

Mon Dec 22, 2008 8:46 pm

Still no callback from JH...

2

1484

Mon Dec 22, 2008 12:39 am

Bad news - MRI results

[ Go to page: 1, 2, 3 ]

34

5151

Sat Dec 20, 2008 8:32 pm

Post new topic

Page 2 of 5

[ 213 topics ]

Go to page Previous 1, 2, 3, 4, 5 Next

Board index » Treatments » Revimmune (cyclophosphamide or cytoxan)

All times are UTC - 8 hours [ DST ]

Who is online

Users browsing this forum: No registered users

	Unread posts			No unread posts			Announcement
	Unread posts [ Popular ]			No unread posts [ Popular ]			Sticky
	Unread posts [ Locked ]			No unread posts [ Locked ]			Moved topic

You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Jump to:

Read hundreds of Multiple Sclerosis stories on Experience Project. Experience Project is community where people connect through their life experiences. It's made by the same people who built This is MS, on the premise that no single life experience-- like having MS-- defines a person. EP covers over 10 million true stories about every possible life experience. Find yours!

Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers | Song Meanings | Stand for your Favorite Causes

This site does not offer, or claim to offer, medical, legal, or professional advice. All treatment decisions should always be made with the full knowledge of your physicians.

All logos and trademarks in this site are property of their respective owners. Content is © 2002-2011 by thisisMS.com.