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I am also on several other list and have been in awe of the response to this

horror. Many people from other countries writing to show their support and

love it is awesome!! One country that has really seemed to be reaching out

at least in the emails I have been reading has been people in Austria. It is

sad that it takes something like this to bring people together but how

awesome it is that we can support and encourage one another when it does

happen. The Internet has really opened up a lot of doors for us to be get to

know people who are not from our country and that we can see how we are all

just humans.

I for one really appreciate all the concern and caring that has been shown.

I do have a sister in law close to DC and we have a good friend who lives in

DC. Though neither of them would have been around the pentagon. I do not

know anyone who lives in NY personally but my heart goes out to them.

I lived in OK at the time of the bombing and the thing that really touched

me the most was to see how people came together and worked so hard to help a

stranger. To see people standing in the rain for hours to give blood. They

even refused to go home when red cross tried to closed for the night and

they ended up working late into the night as the people gave blood to help

people that had never met.

Sometimes I get frustrated with some of the things I see going on around me

then something like this happens yes there are evil crazy people but it is

in seeing the ones that are risking their own lives and the outpour of

support and prayers that overwhelm me and make me see that there is more

than just hope for our country and for others!

blessing to you all!!

Sherry

> Thank you for your e-mail. It is appreciated.

> I am on numerous lists for my different interests and it has been

> touching to have people from other countries write in expressing their

> feelings and support. Even a person from Israel was shocked at the

> magnitude of the act of war.

> It still seems unreal to me, the horror is too much to process.

>

>

>

>

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  • 1 year later...

Who are you thinking of seeing in Fargo??? I live in Moorhead which is

across the river from Fargo. I have a wonderful rheumatologist that I see.

http://albums.photo.epson.com/j/AlbumList?u=4096322

[ ]

> Living in this " small town " everyone knows everyone... not too many

> doctors...and they are partners.... I was thinking of heading to

> Fargo....3 hrs away though so I think I'll give this a try... I have

> been living on Advil which seems to help somewhat.

>

> is there a way to stay with this group but not have email sent?

> I try to get on as much as I can, but don't always get to the mail

> box and it fills up very fast. I love getting all the advice from

> this group and it really is a great support, but would rather read it

> all on the board instead of email. I'm so new to message boards I'm

> not sure I understand too much of how they work.

>

> Thanks

>

> Chris

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I don't have a clue... can you let me know who it is your seeing??

--- In , " Pederson " <linda@7...>

wrote:

>

>

> Who are you thinking of seeing in Fargo??? I live in Moorhead

which is

> across the river from Fargo. I have a wonderful rheumatologist

that I see.

>

>

> http://albums.photo.epson.com/j/AlbumList?u=4096322

> [ ]

>

>

> > Living in this " small town " everyone knows everyone... not too

many

> > doctors...and they are partners.... I was thinking of heading to

> > Fargo....3 hrs away though so I think I'll give this a try... I

have

> > been living on Advil which seems to help somewhat.

> >

> > is there a way to stay with this group but not have email

sent?

> > I try to get on as much as I can, but don't always get to the

mail

> > box and it fills up very fast. I love getting all the advice from

> > this group and it really is a great support, but would rather

read it

> > all on the board instead of email. I'm so new to message boards

I'm

> > not sure I understand too much of how they work.

> >

> > Thanks

> >

> > Chris

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Hi Chris

I see Dr. Carpenter with MeritCare Clinic. He's been great. I have

heard good things about him from others.

http://albums.photo.epson.com/j/AlbumList?u=4096322

Re: [ ]Chris

> I don't have a clue... can you let me know who it is your seeing??

>

>

>

> >

> >

> > Who are you thinking of seeing in Fargo??? I live in Moorhead

> which is

> > across the river from Fargo. I have a wonderful rheumatologist

> that I see.

> >

> >

> > http://albums.photo.epson.com/j/AlbumList?u=4096322

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  • 1 month later...

,

I'm sorry I missed this email and didn't respond earlier. Are you referring

to helping digestion?

I don't know-- I'm sure others have better suggestions than me. A good

enzyme supplement, and lots of it, and some sort of intensive program with

probiotics and only easy to digest foods, maybe some sort of fast, Primal

Defense, and

lots of it, etc. If you have any root canals get them taken care of, etc.

Chris

In a message dated 10/3/03 6:53:48 PM Eastern Daylight Time,

STEVEN.CARROLL@... writes:

> What do you suggest I about tied everything I can think of and more.?

>

> > Subject: Re: Fat soups help required

> >

> > Steve,

> >

> > While I think your first priority should be to treat your digestive

> problems,

> > if that in itself does not lead to sufficient weight gain, you might

want

> to

> > try lifting weights and taking colostrum.

> >

____

" What can one say of a soul, of a heart, filled with compassion? It is a

heart which burns with love for every creature: for human beings, birds, and

animals, for serpents and for demons. The thought of them and the sight of them

make the tears of the saint flow. And this immense and intense compassion,

which flows from the heart of the saints, makes them unable to bear the sight of

the smallest, most insignificant wound in any creature. Thus they pray

ceaselessly, with tears, even for animals, for enemies of the truth, and for

those

who do them wrong. "

--Saint Isaac the Syrian

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  • 1 year later...

Hi Chris:

If you have been dx with RA, you have certainly come

to the right place to talk with people who have the

same illness. Pain in the feet is very common in RA,

and there is no rhyme or reason as to where the RA

will cause pain on any given day for me, but I do have

pain in much more than just my feet. For me, the foot

pain is in the tops of my feet and up into my ankles.

I also take Mtx, but take all of mine at the same time

once a week - do you know why your doctor has you

spread out the dose? How was your RA dx? For me, it

was with physical exam as well as lab work - RA factor

was positive, and other labs were also indicative of

RA. I was dx 6 years ago, and have been on many

different meds - right now I am on Mtx, Enbrel, Mobic

and Tramadol for it.

Perhaps our moderators, or a, could better

address the question as to why you have pain only in

the bottoms of your feet. It does seem strange not to

have pain in any other joints, and yet have been dx

with RA? Anyway, welcome to the group.

Kathe in CA

--- orioles2324 <orioles2324@...> wrote:

> I've had pain in the bottom of both feet for over 3

> years. I had

> Tarsal Tunnel surgery last summer and then was

> diagnosed with RA this

> past winter. I've been taking methotrexate(2.5mg 3x

> 12hrs apart 1st a

> wk), Prednisone(5mg daily)and Celebrex 200mg daily.

> I can get around

> better but am still limited. Is it common to have RA

> only on the

> bottoms of both feet with no other pain. Where can I

> get information

> on this specific issue and talk with someone who has

> the same illness?

> Thanks!!--Chris

>

>

>

>

>

>

>

Kathe in CA

__________________________________

Start your day with - Make it your home page!

http://www./r/hs

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Thanks Kathi,

My RA factor was positive as well. The rest of me body is good to

go..save for depression but that's improving a bit more. I don't

know why my Doc speads out the Mtx.

I've improved enough to start getting on line...finally. Before I

just could not focus. thanks for your welcome!--Chris

>

> > I've had pain in the bottom of both feet for over 3

> > years. I had

> > Tarsal Tunnel surgery last summer and then was

> > diagnosed with RA this

> > past winter. I've been taking methotrexate(2.5mg 3x

> > 12hrs apart 1st a

> > wk), Prednisone(5mg daily)and Celebrex 200mg daily.

> > I can get around

> > better but am still limited. Is it common to have RA

> > only on the

> > bottoms of both feet with no other pain. Where can I

> > get information

> > on this specific issue and talk with someone who has

> > the same illness?

> > Thanks!!--Chris

> >

> >

> >

> >

> >

> >

> >

>

>

>

> Kathe in CA

>

>

>

>

> __________________________________

> Start your day with - Make it your home page!

> http://www./r/hs

>

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Thanks Kathi,

My RA factor was positive as well. The rest of me body is good to

go..save for depression but that's improving a bit more. I don't

know why my Doc speads out the Mtx.

I've improved enough to start getting on line...finally. Before I

just could not focus. thanks for your welcome!--Chris

>

> > I've had pain in the bottom of both feet for over 3

> > years. I had

> > Tarsal Tunnel surgery last summer and then was

> > diagnosed with RA this

> > past winter. I've been taking methotrexate(2.5mg 3x

> > 12hrs apart 1st a

> > wk), Prednisone(5mg daily)and Celebrex 200mg daily.

> > I can get around

> > better but am still limited. Is it common to have RA

> > only on the

> > bottoms of both feet with no other pain. Where can I

> > get information

> > on this specific issue and talk with someone who has

> > the same illness?

> > Thanks!!--Chris

> >

> >

> >

> >

> >

> >

> >

>

>

>

> Kathe in CA

>

>

>

>

> __________________________________

> Start your day with - Make it your home page!

> http://www./r/hs

>

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  • 11 months later...

I think it all depends on your level of illness. from what you've said

before, you may have mcs. I would spend some time around woodstoves

before you waste money on a project that you may find that you can not

tolerate. most mcs'ers can't tolerate wood heat or smoke. if you have

allergies or chronic sinusitis and multiple sensativitys 's way may

not work for you. just my view. someone once said that you cant see

what your mind cannot comprehind, that was a post of 's, yes I did

go and read some of his past posts to try to understand where he was

comeing from. well, I can only say that he doesn't see how different

our illnesses are because he was not exposed to that level. hope it

works out for you.good luck

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