RE: The High Price of the New MS Pill

[Guest guest]

nne, I am already past that stage.  I am in therapy now but

I still can’t get my thoughts under control.  I found a guy on line who asked

my permission to beat me up and I said yes, met him and he did just that,

From: MSersLife

[mailto:MSersLife ] On Behalf Of nne Svihlik

Sent: October-11-10 7:37 PM

To: mserslife

Subject: RE: The High Price of the New MS Pill

Oh I am so sorry to hear about the meds. I have heard

the prices are out of control. I had chemo back in 1990 and I cannot understand

how they can charge the outrageous prices they charge now. You are in my

prayers. Please come here and talk to us. Don't do anything in desperation.

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 Life

http://breastcancerpatientssoulmatesforlife.bravehost.com/

Anxiety Depression and Breast Cancer

http://health.groups.yahoo.com/group/AnxietyDepressionandBreastCancer

Angel Feather Loomer

www.angelfeatherloomer.blogspot.com

The Cancer Club

www.cancerclub.com

RE: The High Price of the New MS Pill

You know, this is really getting out of hand. The one hope I had was

an oral medication being cost effective to people. Now, there is little

hope for that. I cannot afford the current MS meds and now it looks like I am

going to have to win a multi million dollar lottery to even think about an MS

oral medication. I cannot live with MS and all the other life

complications. It is all getting out of hand. Not only with the

side effects of current MS drugs but trying every month to find the money to

pay for it all. I tell everyone now that I am a hooker for the drug companies.

I work for medications first and after, if I have any money left, I pay my

bills. Canadian and provincial programs are a joke here. I

still cannot afford my medications with their co pay system they have based on

my income. They fail to see any income coming in is going straight back

out for drugs. It all sucks. I have told my family that if I get

anymore bad news about my health that is chronic or life altering, I am going

to disappear and live my life off the grid until I die ... I can’t it anymore.

Between MS, diabetes, hypothyroidism, arthritis, depression, anxiety,

migraines, undiagnosed cause of daily dizzy spells, my ear problems, my eye

problems and pharmacies not being able to fill my prescriptions because the

drug companies cannot make them fast enough or, I have had

enough.

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[Guest guest]

What?!?!?!?!?

~*~Hugs~*~

~*~Akiba~*~

-- RE: The High Price of the New MS Pill

nne, I am already past that stage. I am in therapy now but I still can’t get my thoughts under control. I found a guy on line who asked my permission to beat me up and I said yes, met him and he did just that,

From: MSersLife [mailto:MSersLife ] On Behalf Of nne SvihlikSent: October-11-10 7:37 PMTo: mserslife Subject: RE: The High Price of the New MS Pill

Oh I am so sorry to hear about the meds. I have heard the prices are out of control. I had chemo back in 1990 and I cannot understand how they can charge the outrageous prices they charge now. You are in my prayers. Please come here and talk to us. Don't do anything in desperation.

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: koala5@...Sent: Mon, 11 Oct 2010 17:54:12 -0400To: mserslife Subject: RE: The High Price of the New MS Pill

You know, this is really getting out of hand. The one hope I had was an oral medication being cost effective to people. Now, there is little hope for that. I cannot afford the current MS meds and now it looks like I am going to have to win a multi million dollar lottery to even think about an MS oral medication. I cannot live with MS and all the other life complications. It is all getting out of hand. Not only with the side effects of current MS drugs but trying every month to find the money to pay for it all. I tell everyone now that I am a hooker for the drug companies. I work for medications first and after, if I have any money left, I pay my bills. Canadian and provincial programs are a joke here. I still cannot afford my medications with their co pay system they have based on my income. They fail to see any income coming in is going straight back out for drugs. It all sucks. I have told my family that if I get anymore bad news about my health that is chronic or life altering, I am going to disappear and live my life off the grid until I die ... I can’t it anymore. Between MS, diabetes, hypothyroidism, arthritis, depression, anxiety, migraines, undiagnosed cause of daily dizzy spells, my ear problems, my eye problems and pharmacies not being able to fill my prescriptions because the drug companies cannot make them fast enough or, I have had enough.

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[Guest guest]



,

your email has me very concerned as well...I know I don't really know you yet, but I would like the chance to get to know you. I can tell just how purely frustrated you are and you are completely and totally overwhelmed here......I wish there was something I could do for you, or say to you, I really do....

how supportive IS your family? do they not offer you any help at all?? I am blessed to have a huge support system in my family and friends and more than enough people I know will be there for me when and if I ever need them....so it hurts me to see YOU hurting so.......

i wish i were near you so i could assist you somehow to make your life easier, i really do..........

big, big hugs.........

Jen

RE: The High Price of the New MS Pill

You know, this is really getting out of hand. The one hope I had was an oral medication being cost effective to people. Now, there is little hope for that. I cannot afford the current MS meds and now it looks like I am going to have to win a multi million dollar lottery to even think about an MS oral medication. I cannot live with MS and all the other life complications. It is all getting out of hand. Not only with the side effects of current MS drugs but trying every month to find the money to pay for it all. I tell everyone now that I am a hooker for the drug companies. I work for medications first and after, if I have any money left, I pay my bills. Canadian and provincial programs are a joke here. I still cannot afford my medications with their co pay system they have based on my income. They fail to see any income coming in is going straight back out for drugs. It all sucks. I have told my family that if I get anymore bad news about my health that is chronic or life altering, I am going to disappear and live my life off the grid until I die ... I can’t it anymore. Between MS, diabetes, hypothyroidism, arthritis, depression, anxiety, migraines, undiagnosed cause of daily dizzy spells, my ear problems, my eye problems and pharmacies not being able to fill my prescriptions because the drug companies cannot make them fast enough or, I have had enough.

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[Guest guest]



Wow Sharon, I am very sorry to hear this too

Jen

Re: The High Price of the New MS Pill

Dear I hear you loud and clear. I am in the same boat as you are now. I used to have really good, affordable insurance but now the insurance is so expensive I can't afford it. I don't want to get all political here but the reason the cost of my insurance went up is because of the first of the new rules for our new universal insurance coverage. I think the main reason for the increased costs is that now every insurance has to cover adult children on their parents policy up to age 26. That has really raised the costs to the insurance company. My insurance cost doubled. I don't qualify for Medicaid (free) so I am out of luck.I also thought well when the oral med comes along maybe I'll be able to afford that. Ha! love to you

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