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07-22-2009, 06:43 PM | #31 | ||
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The link wouldn't post, but it's on google: MS Breakthrough?
February 10, 2009 2:31 PM Edwin McClure contracted Multiple Sclerosis as a high school senior but after undergoing new stem cell treatments, his family says he is "cured." Debbye Turner Bell reports. |
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10-26-2009, 01:21 PM | #32 | ||
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Call 888-477-2669 Partnership for Prescription Access. They will direct you to the proper drug company that carries the drug you are prescribed.
If you need Wellbutrin, call 1-866-728-4368. Baclofen, Klonopin & Xanax and a number of other drugs comes from Rx Outreach; but most importantly it includes the middle income people. 1-800-769-3880. You can even have Part D coverage which doesn't cover Xanax or Klonopin and get these drugs if your income allows; 1-800-769-3880. Help from MS disease modifying drugs: AVONEX: 1-800-456-2255 BETASERON: 1-877-836-5724 COPAXONE: 1-800-887-8100 NOVANTRONE: 1-877-447-3243 REBIF: 1-877-447-3243 TYSABRI: 1-800-456-2255 I have tried to post National MS Society's sites but they keep changing; the best I can recommend is go to their main site and use their search engine to find information you are looking for. |
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08-07-2010, 05:19 PM | #33 | |||
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Legendary
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If you have small children, or grandchildren, and have been looking for an easy way to explain MS to them, try this website from The National MS Society. It's interactive and has been formulated especially for the little ones.
Keep S'myelin: A Fun Resource for Kids about MS http://main.nationalmssociety.org/KS...ue1/index.html
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Eastern Australian Daylight Savings Time and my temperature . |
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04-03-2011, 05:21 PM | #34 | ||
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Are there any clinical trials listed for CCSVI? I didn't find any. It helped my daughter so much.
Thanks |
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11-07-2011, 03:05 PM | #35 | |||
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Wisest Elder Ever
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I inquired about possible assistance from the NMSS for medical equipment and received this very helpful email. It has lots of assistance options and links with valuable information. I wanted to share it here so others could take advantage of the help offered. Here it is:
There are a variety of resources that might be able to help fund a piece of assistive technology or durable medical equipment, like a rollator. I have included information about the process and possible funding sources in the email below in addition to including information about our financial assistance application. PROCESS: Please see these articles for some basic information about theprocess: Finding the Right Stair Lift, Ramp, and Wheelchair : National MS Society Affording Stair Lifts, Ramps, and Wheelchairs : National MS Society POTENTIAL FUNDING RESOURCES: NATIONAL MS SOCIETY’S FINANCIAL ASSISTANCE PROGRAM: The National MS Society has a limited financial assistance program that can be used for an MS-related expense, like assistive technology or durable medical equipment. We ask that you access your health insurance and community resources first, but please feel free to apply to our program if you need assistance. I have attached our cover letter and application above. Note: you will want to return the completed application to the contact information listed on the cover letter. Do not return it to me, as I am in a different office. COMMUNITY RESOURCES: Here is information about four organizations that are often able to help: Multiple Sclerosis Foundation (MSF) 6520 N. Andrews Avenue Fort Lauderdale, FL 33309 Phone: 888-673-6287 Fax: 954-351-0630 Email: support@msfocus.org Website: http://www.msfocus.org/ Eligibility: Persons with MS who have need for financial assistance for equipment or services. An application is required for most of MSF’s grant programs. Services Information: The MSF offers the following financial assistance programs:
MS Association of America: 706 Haddonfield Road Cherry Hill, NJ 08002 Phone: 800-532-7667 Fax: 856-661-9797 Email: msaa@msassociation.org Website: http://msassociation.org/ Eligibility: Persons with MS who need financial assistance for cooling vests, MRI exams and personal use equipment. Also serves people who need an initial MRI to establish a diagnosis of MS. An application is required for each MSAA grant program. Services Information: The MSAA offers the following financial assistance programs:
Friends of Man P.O. Box 937 Littleton, CO 80160 Phone: 303-798-2342 Website: http://friendsofman.org/ Eligibility: Applications are accepted from U.S. residents and must be submitted by an agency on behalf of the individual. Rent, utilities, deposits, past due bills and reimbursement are not eligible requests for this program. Services:
ModestNeeds.Org 115 E 30th Street, FL1 New York, NY 10016 Phone: 212-463-7042 Website: http://www.modestneeds.org/help/grants/ Eligibility: § At least 18 years of age § Legal resident of the United States or Canada § Intend to apply for assistance either for yourself, or for a person living in your home § Household has at least one active bank account § Have regular access to a computer and the Internet and can check your email the Modest Needs website daily for the entire time that your application is active; § Have the ability to access either a scanner or a fax machine at my home, my place of business, or a shop like FedEx Business or Office Max for long enough to send the documentation that Modest Needs will request from me during the grant application process to Modest Needs' office for evaluation; and, if you rent (rather than own your residence) § Household has a legal lease that my landlord and a member of your household both have signed. This lease shows the monthly cost of your apartment, whether or not you pay all of this amount. Services Information: Offers the following types of grants:
I hope this information is helpful. If you have any other questions or concerns, please do feel free to contact us by phone at 1-800-344-4867 or by email at contactusnmss@nmss.org to have an MS Navigator assist you.
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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"Thanks for this!" says: | msbluis (05-10-2014) |
03-07-2013, 03:39 PM | #36 | |||
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Senior Member
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Some of this is a repeat:
Here are some companies that might be useful to help pay for medications: Montel Williams MS Foundation: (888) 324-2773 Partnership For Prescription Assistance: (888) 477-2669 Wellness 2 Wellness: (866) 317-2775 Together RX Access: (800) 444-4106 The Commonwealth Fund: (212) 606-3800 The Medicine Program: (800) 921-0072 NeedyMeds: (978) 865-4115 National Organization of Rare Disorders (NORD): (203) 744-0100 Rx Council: (866) 794-3571 Alternative Funding Group: (866) 426-2906 Patient Access Network: (866) 316-7261 Bridges to Access: (866) 728-4368 Rx Outreach: (800) 769-3880 Look above in this thread for the phone numbers to the DMDs' patient assistance programs.
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RRMS, diagnosed '00 Everything will be alright in the end. If it's not alright, it's not yet the end. |
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"Thanks for this!" says: | SallyC (03-07-2013) |
04-30-2013, 06:20 PM | #37 | |||
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Member
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I just saw my neurologist today (every 6 months since I'm on Tysabri). He is at a big medical school and does research as well. He has been reading research on copper and zinc deficiencies which are associated with demyelinating disorders.
He and the NIH are doing research on the JCV antibody test. They used to think the false negative rate was 2.5 %. Now it could be more like 10-12%. In other words, some people who were negative are becoming positive (he didn't say how many cases). They are trying to figure out why this is happening. He's now adding a PCR test for the virus with every infusion (I get them every 8 weeks) which looks for JC virus DNA in your blood. It's a way, on an offhand chance, to pick up the virus in your body if you have a false negative situation going on. They also think the problem might be there is more than one strain of JC virus so the assay test might not be picking up the strain you have, or maybe your body doesn't produce the antibodies in a great enough number to register on the assay (test). They think that maybe only one particular strain causes PML. He said it will take a year for them to sort all of this out. He said this spring they refined the JCV antibody test so I will get the new one at my next infusion. I think it has been refined to catch some of the false negatives. I can't remember how exactly the test has been made better. Thought I would share!
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On Tysabri and love it. . |
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"Thanks for this!" says: | SallyC (04-30-2013) |
05-10-2013, 06:07 PM | #38 | |||
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Wise Elder
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Great, informative site for both newbies and experienced MSers. Lots of information on this site and I recommend it to anyone seeking more info on MS.
http://my-ms.org/ms.htm |
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"Thanks for this!" says: | SallyC (05-10-2013) |
10-13-2013, 12:13 PM | #39 | |||
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In Remembrance
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A good article about LPs, from Web MD.....
www.webmd.com/multiple-sclero...13_promo_1&mb= And Evoked Potentials... http://www.webmd.com/multiple-sclero...otential-tests
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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"Thanks for this!" says: | Kitty (10-13-2013) |
04-19-2015, 12:58 PM | #40 | ||
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Junior Member
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http://www.neurology.org/content/82/...t/P3.155.short
Study has been going approx. 1 year, Pilot Trial Of Recombinant Human Growth Hormone For Remyelination In Multiple Sclerosis: Current Status And Preliminary Safety Analysis (P3.155) Dr. Then Bergh has received personal compensation for activities with Biogen Idec, Novartis, Merck Serono, and Sanofi-Aventis Pharmaceuticals Inc. as a speaker or member of an advisory board. Dr. Then Bergh has received research support from Bayer Schering, Novartis and Teva Neuroscience. In other words, every large Pharma is interested in the outcome of this one.. I am too. |
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