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Hey, I'm blood type O- ! Interesting, I didn't know that about type

Os. O is one of the rarer blood types, isn't it? Or maybe I'm just

thinking of O negative. Anyway, would love to hear more about that

book, .

>I'm reading the book 'Eat

> Right for Your Blood Type' and it makes soooo much sense. If you

don't mind

> me asking - are you a type O? I'm also wondering if any of the rest

of you

> guys are b/c it says that O's are prone to autoimmune disease and also

> thyroid disorders. I'm very curious if any of you are O's. I'll

write more

> about it if anyone is interested.

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Somehow I missed the original message about the blood types, but it's VERY interesting! I am an o- ! (Another thing we have in common, !)

Definitely write more about this!!

Thanks,

Miaja**

Bella Luna ToysBringing Imagination Into Play!www.bellalunatoys.com

-----Original Message----- Sent: Sunday, February 02, 2003 8:43 AMTo: Thyroiditis Subject: Re: HelloHey, I'm blood type O- ! Interesting, I didn't know that about typeOs. O is one of the rarer blood types, isn't it? Or maybe I'm justthinking of O negative. Anyway, would love to hear more about thatbook, .>I'm reading the book 'Eat > Right for Your Blood Type' and it makes soooo much sense. If youdon't mind > me asking - are you a type O? I'm also wondering if any of the restof you > guys are b/c it says that O's are prone to autoimmune disease and also > thyroid disorders. I'm very curious if any of you are O's. I'llwrite more > about it if anyone is interested.

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Hi ,

I'm new to the list. I have read the book you are referencing and yes, I am type O, as are all of my children.

Our GP wants to test my ten year old son for thyroid disease.

I was diagnosed in 1993 and had a partial thyroidectomy in 1994.

I really thought about giving in and eating as prescribed by the book but I was not ready to give up mushrooms.

And that's the truth. Isn't that sad? LOL.

Marta

-----Original Message-----From: Pierce Sent: Sunday, February 02, 2003 10:53 AMTo: Thyroiditis Subject: Re: HelloFish oil capsules are good for lowering triglycerides. It did help my sister. I take the Carlson's brand (Omega 3). I'm reading the book 'Eat Right for Your Blood Type' and it makes soooo much sense. If you don't mind me asking - are you a type O? I'm also wondering if any of the rest of you guys are b/c it says that O's are prone to autoimmune disease and also thyroid disorders. I'm very curious if any of you are O's. I'll write more about it if anyone is interested. write back please about that if you don't mind :)

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What book are you all talking about, I have been reading the post. I was diagnosed with Hashi's in October of last year

and I am still learning. I am taking synthroid, does anyone use alternative medicine for their hashi's?

-----Original Message-----From: Pierce Sent: Sunday, February 02, 2003 1:22 PMTo: Thyroiditis Subject: RE: HelloMarta,portobella mushrooms are allowed and they're sooo yummy. There's lots of things that I'm upset about giving up, but I have to do it!_________________________________________________________________STOP MORE SPAM with the new MSN 8 and get 2 months FREE* http://join.msn.com/?page=features/junkmail

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  • 1 year later...
Guest guest

Dear Recent Posters,

I am going to write one big email to address some of the recent

posters today, ok?

Patti, you haven't mentioned the wrist/hand problem. What up with

that? It breaks my heart to know you have to have help doing stuff

around the house because I know how independant and self sufficient

you are. Eventually the meds will be figured out and you will improve.

This is my hope for you. I have heard stories--some on this very group

--of those who were in awful shape and came back from it. Don't give

up and keep working with your doctors. It sounds like they have a

plan. Keep up your great attitude!!

Sandy, Since I haven't figured out the EN cure yet (and I have not by

any means given up) I hope we can all discover ways to lengthen our

remissions and make the flare-ups briefer and less severe. I am having

such fine results with the anti-embolism stocking and once your

current flare-up has subsided, perhaps you will give it a try.

Putting the stocking on while in flare-up is painful, but I think

wearing it between flares is helping to keep the edema down and that

in turn may be less stimulating to the immune cell clusters. This is

just a theory of course--one of many on this site. I am still eating

garlic and using the peroxide gel on my teeth, which may be addressing

hidden strep infection.

Sharon, I have many different sized shoes in my closet too. I have the

situation of having one EN leg only. When that foot swells I wear a

loose shoe and put an insert in the other shoe to take up the slack.

I have a pair of black canvas " mary-janes " that are so comfy. Mostly

they give the illusion of wearing shoes. They are really just

glorified slippers.

It is nearly 3 months since my last EN flare up. This is the longest I

have gone in a very long time. I do have a question. For those who are

using the TEDS stockings, how do you keep them up? Garter belt? Mine

seem to slip when I go for walks even though there is a wide elastic

band high on the thigh. If I wore the smaller size, I know it would be

uncomfortably tight.

Lots of us are in pain as we approach the weekend. I hope we will all

get rested and relax, and find reason to be happy in spite of the pain

and discomfort.

I thank all of you for your participation in this group. The support,

and exchange of ideas is what makes our group so special.

Love,

(idiopathic EN)

> > > > Well I finally started to desensitize back onto SSKI

> > yesterday.

> > > Have

> > > > done 2 days worth and have 2 days to go. I have not broken

> > out in

> > > > hives nor have I started to itch. I would think these would

> > be

> > > great

> > > > fantastic signs. Problem???? I have completely broken out

> in

> > a

> > > > major flare up of EN. I don't know if this desensitation is

> > > causing

> > > > this or not. I do see my dermatologist on Tuesday and I am

> > off of

> > > > work tomorrow so I was just going to rest a bit. But I'm in

> > pain

> > > and

> > > > can't get comfortable. The nurse I worked with today really

> > > wanted

> > > > me checked out at the ER, but how many visits does a person

> > have

> > > to

> > > > go through for them to really say, ummm...there really isn't

> > > anything

> > > > we could do for you. I will wait patiently till Tuesday,

> get

> > tons

> > > of

> > > > injections and discuss if the desensitizing caused this. I

> > pray

> > > it

> > > > did not. Going back on the SSKI is about my only hope

> here.

> > Oh

> > > > well, I guess if SSKI is causing it, at least I know not to

> > touch

> > > the

> > > > stuff in the future.

> > > >

> > > > Besides steriods, what other medications is everyone taking

> > that

> > > is

> > > > working for the EN?

> > > >

> > > >

> > > > the lumpy sore zoo

> > >

> > >

> > >

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Guest guest

> It is nearly 3 months since my last EN flare up. This is the longest I

> have gone in a very long time. I do have a question. For those who are

> using the TEDS stockings, how do you keep them up? Garter belt? Mine

> seem to slip when I go for walks even though there is a wide elastic

> band high on the thigh. If I wore the smaller size, I know it would be

> uncomfortably tight.

I was told to wear mine (prescribed for vasculitis which is what my

" EN-like " symptoms were described as causing) DURING a flare up to keep the

veins compressed so blood flows normally instead of " leaking out " causing

the edema/swelling. I had mine fitted at a medical supply house - they are

supposed to be very snug (there are varying degrees of compression depending

upon the problem) but feel pretty good after they have been on for 15

minutes or so. If fitted properly, and not stretched out of shape by

improper care, loss of elasticity, or putting them on incorrectly (they

should be kind of rolled up the leg) etc. they should stay up by themselves.

Mine come just to the top of my knees and my legs were measured for both

length from heel to calf and heel to knee to get the length; the

circumference of my largest leg was also measured at the ankle and the

widest part of the calf.

Though I've still got the bruised look where I had lumps a year ago, the

lumps have not returned. If I press on my leg, what should be soft fatty

tissue is somewhat hardened but " lumpless " on the surface.

Sue

---

Outgoing mail is certified Virus Free.

Checked by AVG anti-virus system (http://www.grisoft.com).

Version: 6.0.662 / Virus Database: 425 - Release Date: 4/20/2004

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  • 4 months later...

Has your boyfriend tried using a support stocking?

Greetings Robin

My wife just snuck some in our basket as Wal Mart Thursday.

They are great and comfortable and your boy friend might like them

I have three different colors.

Now I can mix and match.LOL

I wear them for blood clots in my legs.

Friends,

Jim /cns vasculitis

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Dear Robin,

We on this group are doing everything we can to make that day come

soon! I think of EN as a puzzle, and all of us have a tiny piece of

that puzzle...a part that may be exactly what we need to figure it

out. By sharing information we are learning so much more than we could

alone.

Has your boyfriend tried using a support stocking? I know it may be

difficult when there is a lot of pain and swelling, but it does help

to reduce the swelling, and rather quickly. An ACE bandage can also be

used and it can be wound as loosly as needed for comfort. I have been

wearing a TEDS stocking with great success. I only get EN in my left

leg, and so I only wear one stocking. I call it a " fashion statement "

:-). I have felt so much better since using it, and right now I am in

a nice remission without taking meds.

Please give your boyfriend our best regards, and wishes for getting

into remission and feelling better soon.

Love,

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  • 4 years later...

Its mutual I guess :-)

Ravin '82

> Ravin Sir,

> Its really nice to know a friendly person like you.

>

> With regards and good wishes,

>

> Amit Kant Singh

> Lecturer,

> Incharge Male Infertility and Reproductive Physiology Unit,Dept. of

> Physiology,

> Consultant Male Infertility Clinic, Dept. of Urology,

> Institute of Medical Sciences,

> Banaras Hindu University,

> Varanasi 221005 India

> E mail:- amitbhu08@...

>

>

>>

>> > Dear Sir/ Madam,

>> > I was surfing through the web there I came across the mgims e group. Its

>> a

>> > lovely site.The photo section is so good that we feel the real

>> > liveliness

>> of

>> > our Alma Mater.

>> > With regards and good wishes to All.

>> >

>> > Amit Kant Singh

>> > Lecturer,

>> > Incharge Male Infertility and Reproductive Physiology Unit,Dept. of

>> > Physiology,

>> > Consultant Male Infertility Clinic, Dept. of Urology,

>> > Institute of Medical Sciences,

>> > Banaras Hindu University,

>> > Varanasi 221005 India

>> > E mail:- amitbhu08yahoo (DOT) com <amitbhu08%40yahoo. com>

>> >

>> >

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dEAR rAVIN, Amit is right. The sniors say that don't call

me sir and what not but even when we write to our seniors SIR comes

automatically, perhaps it is genetically inherited in MGIMS.

Gursharan

> Its mutual I guess :-)

>

> Ravin '82

>

>

> On Tue, Oct 21, 2008 at 12:14 PM, Amit Singh

<amitbhu08@...<amitbhu08%40yahoo.com>>

> wrote:

> > Ravin Sir,

> > Its really nice to know a friendly person like you.

> >

> > With regards and good wishes,

> >

> > Amit Kant Singh

> > Lecturer,

> > Incharge Male Infertility and Reproductive Physiology Unit,Dept. of

> > Physiology,

> > Consultant Male Infertility Clinic, Dept. of Urology,

> > Institute of Medical Sciences,

> > Banaras Hindu University,

> > Varanasi 221005 India

> > E mail:- amitbhu08@... <amitbhu08%40yahoo.com>

> >

> >

> >>

> >> > Dear Sir/ Madam,

> >> > I was surfing through the web there I came across the mgims e group.

> Its

> >> a

> >> > lovely site.The photo section is so good that we feel the real

> >> > liveliness

> >> of

> >> > our Alma Mater.

> >> > With regards and good wishes to All.

> >> >

> >> > Amit Kant Singh

> >> > Lecturer,

> >> > Incharge Male Infertility and Reproductive Physiology Unit,Dept. of

> >> > Physiology,

> >> > Consultant Male Infertility Clinic, Dept. of Urology,

> >> > Institute of Medical Sciences,

> >> > Banaras Hindu University,

> >> > Varanasi 221005 India

> >> > E mail:- amitbhu08yahoo (DOT) com <amitbhu08%40yahoo. com>

> >> >

> >> >

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