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Get Moving 200,000 Signatures Needed December 07, 2006 5:32 AM


http://capwiz.com/nmss/issues/alert/?alertid=9167296&queueid=[

Action Alert

Petition Drive to Increase Federal Funding for MS Research


Sign On and Send to a Friend

More federal funding for medical research is desperately needed to investigate multiple sclerosis. Scientists do not fully understand its causes, therefore an aggressive investment in medical research could lead to a more treatable, and potentially curable, disease.

The National MS Society is circulating this petition to collect at least 200,000 signatures from people who support additional federal funding for medical research for MS. If you know someone with MS or would like to help end its devastating effects, sign the petition by filling out the form below. Then forward it to someone you know.

MS is a chronic, often disabling disease in which the body attacks itself, resulting in damage to the nervous system. Symptoms can be mild, such as numbness in the limbs, or severe with paralysis or loss of vision. Most people with MS are diagnosed between the ages of 20 and 40, the prime years of their lives. The disease course is unpredictable for each person diagnosed with MS, but for every person with MS, the physical and emotional conditions of the disease also impact their families, their jobs, every part of their well-being. By making this commitment to medical research, we can help people with MS and their families.


To Sign the Petition Today, Just Fill Out the Form!

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 December 07, 2006 6:57 AM

I hope that soon MS will beiong to history . They'll say : "once upon a time there was a disease . . . ."

Then we'll be very happy , also many people around us ;

Lots of love , Theo  

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 December 12, 2006 12:56 PM

This petition is for US nationals.... I wish you good luck in this endeavour. There must be an answer.

If only we applied good healthy habbits I just wonder if it would have made a difference.

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 January 06, 2007 4:21 PM

Signed! I don't have MS (I don't think!) however, I have chronic pain and a good friend with MS. She seems to be coping very well with it, runs an animal rescue agency. I also watch Montel Williams and consider the way he handled talking about MS on his show heroic. I've heard of new medications coming out for MS and hope these show some promise for patients.  [ send green star]  [ accepted]
 
Thanks, Theo! January 09, 2007 5:36 AM


I think we all hope that MS and all such horrible diseases and afflictions end in our lifetime!

Please spread the word, so our friends and loved ones can join the fight, too!!

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Thanks, Yvonne! January 09, 2007 5:56 AM


We all hope that MS and all such horrible diseases and afflictions end in our lifetime! In the meantime, every nation must be working on searching for cures, and for providing coping strategies for those afflicted with MS and other such diseases. Alternatives certainly fall into the category of "helping".

Please spread the word, so our friends and loved ones can join the fight, too -- but also make sure every government is moving forward by funding the search for cures as well as providing comfort while we all try to live "normal" lives!!

As you'll find in reviewing other threads, this is an international effort, as it must be, because MS and other afflictions are international curses.

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Thanks Jennie, January 09, 2007 6:12 AM


for signing and for joining!!

I've seen studies that suggest that what we call Multiple Scleroses is as many as three diseases. ALS ("Lou Gehrig's disease") may be closer than people think, as well.

Pain management is certainly an issue for many folks with MS.  From those who just suffer from muscle inflexibility and resulting pain, to those like Montel, (and you), who who suffer excruciating, debilitating pain every day, we have a common problem, and it is all too real!!


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I signed and forwarded... February 14, 2007 7:33 PM

Hi,

My name is Elle and I was dx in September of this past year.  The MRIs say I have had MS for at least ten years and never knew!  I thought the intermittent inability to walk was related to three herniated discs in my spine and neck caused by an assault and robbery.   My left leg became paralyzed in late August and that put me in the hospital.

I can walk fairly well, and I can go to the grocery store, etc.  I can take care of my home and my pets - including 3 horses.  I rescue horses that were on their way to slaughter and I can still ride them and rehab them and I was pleased to find an alternative modality is horseback riding!  Now my horses whom I have saved, can help me! 

The one thing I cannot do is write.  I am unable to read my own handwriting and this has put an obstacle to filling out job applications!  Very frustrating.

I am taking Copaxone every day and it is fine.  I don't mind injecting myself and I haven't missed a single dose.  Since I was unemployed at the time of the major attack, I don't have health insurance.  NORD has sponsored the copaxone for a year. 

I can feel the signs of an attack coming on, but it does not really come out all the way.  Of course, the major attack that led to hospitalization and diagnosis was in the middle of a heatwave and it was 95 degrees in my condo.  My A/C works, but the building has settled and if I had run the air, it would not have cooled anything off!

I do get fatigued easily, and I don't like that.  But, I have the most common form - Relapsing and Remitting - and I find myself fortunate because I have a male friend who has primary progressive and he's not doing so well.

I am very glad to have found this group!  Be well and keep well!!!



elle

Manes and Tails Org.


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