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Carol,

I used to have this happen with my CII, and it turned out it was the RF. I

know the Auria and the CII are different, but I think your audie should be able

to fix your problem.......

S.

CII 5/01

~~~~~~~~~~~~~~

----- Original Message -----

From: cbm_1933

I posted this earlier but no replies. My processor is cutting out

and I wondered if any of you had similar problem? It is not related

to any noise or loud sound. It cuts out when it is quiet; when I may

be speaking; when some one else may be speaking; or if I am just

riding along in silence in the car. any time. Dead space lasts

about 4 seconds. It can occur several times close together and then

not occur again for hours. It started on 2nd mapping day when I was

switched to the BTE Auria. We thought it was batteries not fully

charged but all batteries now fully charged and also happens on any

and all batteries. I also changed head pieces thinking maybe short

in the cord but that did not correct it either. I see my audie

Friday for third map and she knows about it and is checking with AB

and will also check all my programs but if any of you have had

similar experience please let me know so I can share with my audie.

thanks for any help.

Carol,

AB K90 12-17-03

Auria 1-13-04

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Donna, did you read the " draft letter to new members " that was just posted

yesterday??? It explains how the group works, how to change your

settings, etc.

You can see it here:

achalasia/message/15155

Of particular importance is the part where it tells you how to adjust your

email preferences.... I'll cut and paste that below for you. Nobody can

control your membership except for you -- a few mouse clicks is all

it takes to either go 'no mail' or unsubscribe from the group altogether.

There's no need to be bombarded with emails if you don't want to receive

them.

Debbi

-----------------------

You can change your email settings at any time by using the " Edit My

Membership " link on the upper right side of any group webpage. You may

change the email address to any other address you may have (which requires

you to " verify " the address by replying to an email that will send

to the alternate address.) [Please be aware that any address you use to

post to the group will be visible via the internet to the public and to

other group members via email.]

You can also change the frequency with which you receive emails.

" Individual Emails " means that each time someone posts to the group via

website or email, you will receive an email containing that post. " Daily

Digest " means that the day's posts will accumulate into one big email, one

message listed after another. At the end of the day (or more often if

there are more than 25 messages in any given day), will send this

one long email to your inbox. " No Email " means just what it says -- no

emails will be sent to you, and you will have to read each message on the

website's " Messages " page.

-----------------------

> Hi All,

>

> just for now I need to stop all of this email bombarding me - this group

> has been extremely helpful, but I need to move on. I have tried to follow

> the strps for removal, evening replying to the email they send u - but

> that was 2 weeks ago & I am still getting all of this email that I am not

> coping with. Does anyone have any suggestions please?????

>

> Donna

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Hi ;

I have SD and the generic worked just beautifully for me.I live in

Canada and we still have the Weth brand here.I hear it was sold to

Triax in the States.Steifel is also a good brand. Lynne

nicole jordan wrote:

> Hi everybody

> Just when I thought I was on the right track, my medical plan

> doesn't cover the Minocin, so Doc gave me Minocycline (generic). Has

> anyone used it and got same results?I read in one of the testimonies

> that you should use only name brands, so I'm concerned. Thank you in

> advance.

>

>

> ---------------------------------

> Feel free to call! Free PC-to-PC calls. Low rates on PC-to-Phone. Get

> Messenger with Voice

>

>

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,

The paragraphs below are from one of my 2002 postings. Since that

time, there has been little feedback from our group. It appears that

all generic minocyclines are not the same when it comes to RA, but

most of the time people who are taking a generic drug do not know its

manufacturer.

" The question of which generic brands of generic minocycline work for

RA keeps coming up in our group, but there have been more questions

than answers. A number of people have shared that they had to go back

to brand-name Minocin because " the generic " did not work for them --

but without providing the name of the manufacturer. A problem is that

brand-name Minocin is 4 1/2 time mores expensive than the generics.

I hereby volunteer to maintain the web page

www.tmgp.com/generic-mino.htm page to summarizes feedback on the

efficacity of generic minocyclines for RA. To share your experience,

please send your feedback to rheumatic . Please do

this now, even if you have already sent this information to the group

in the past. Be sure to include the manufacturer of the generic that

you have taken or are now taking. If you do not already know this

information, please ask your druggist.

In August 2000, Dr. Mercola wrote, " Clinical experience has shown

that many patients will relapse when they switch from the brand name

to the generic. Clinically it has been documented that it is

important to take Lederle brand Minocin. Most all generic minocycline

is clearly not as effective. A large percentage of patients will not

respond at all or not do as well with generic non-Lederle

minocycline. " Please see

http://www.mercola.com/2000/aug/27/Rheumatoid Arthritis.htm

There are a number of manufacturers of generic minocycline, and the

same drugstore may be carrying different manufacturers. If you do not

specify a manufacturer, the druggist will pull the generic of his/her

choice. Independent drugstores, as opposed to chain drugstores, may

be able obtain the generic from specific manufacturer upon request.

Also, different drugstores will charge differently for the same drug.

I found that my local independent drugstore was willing to match

Wal-Mart's pricing. "

***

The pelleted Minocin was developed by Lederle Labs, which became ESI

Lederle, which was acquired by Wyeth-Ayerst Laboratories, which then

changed its name to simply to Wyeth. Minocin by Lederle, ESI Lederle

and Wyeth were all the same thing. In early 2006, Wyeth sold its

Minocin product line to Triax Pharmaceuticals. Hopefully brand name

Minocin will remain what it has always been.

Sincerely, Harald

At 10:33 AM 5/25/2006, nicole jordan wrote:

>Hi everybody

> Just when I thought I was on the right track, my medical plan

> doesn't cover the Minocin, so Doc gave me Minocycline (generic).

> Has anyone used it and got same results?I read in one of the

> testimonies that you should use only name brands, so I'm concerned.

> Thank you in advance.

>

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It is a result of hyper activity of the spleen...so anything that causes

an unusually high amount of red blood cell destruction will lead to

enlargement. Anemia is a good example of that.

Is it something your doc will try to control, or has removal been

suggested?

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>

> It is a result of hyper activity of the spleen...so anything that

causes

> an unusually high amount of red blood cell destruction will lead to

> enlargement. Anemia is a good example of that.

>

> Is it something your doc will try to control, or has removal been

> suggested?

>

>

>

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>

> I have just been dx with splenomegaly does anyone have this with

hep.c?

> or is it something else wrong with me???

>

Yes I had to go to the ER this week for it so they say, I'll see my GI

Doc on the 22nd and learn more, All I know is I felt sick and pain in

left side.

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Shrugged his shoulders???? Are you kidding me????

Time for a new doctor first and foremost....

Don't allow yourself to be treated that way.

Are you in a position to seek a second opinion?

I would start there. You need to know exactly what

function of your spleen is compromised.

so sorry for your experience..

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,

Depression is one of the common symptoms of rheumatoid arthritis

along with joint stiffness and fatigue. It is likely that after two

months on the AP, you experiencing a Herxheimer reaction, during

which RA symptoms will actually be worse. The good news is that the

Herxheimer reaction is only temporary and is a good thing, proving

that the AP is working. After another couple of months, you should

start getting better and better. So cheer up!

Sincerely, Harald

At 06:00 PM 6/28/2006, you wrote:

>Has anyone experienced depression, i mean really bad, when starting

>the AP? I am in my second month and this started about 3 wks ago. I

>am at loss, since i've never felt this low before. Besides the

>tiredness, it's a major blow.

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Vit C helped us with this problem.

HELP!!!!

I am brand new to this group. My son has been consitpated most of his

young life (he is 4 and a half now). He has been on and off Miralax,

Kondremul, and senna drops. Nothing seems to help. I have been to

two GI specialists. One told me it is a result of functional stool

holding. Since they associate bowel movements with pain they tend to

hold their stools in. This just aggravates the problams.

I am ready to try anything.

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...my daughter has suffered with chronic constipation since infancy

as well (she is now almost 6). You should join the

group " Miralax " - it is all people who have children with chronic

constipation that are trying to (or have succeeded) in getting their

kids off Miralax. It is a wealth of info. I recently got my daughter

off Miralax after being on it for 5+ years. We've done it mostly with

the addition of Natural Calm (a magnesium citrate product). Mind you,

we also have had her on vitamin/mineral supplementation, probiotics,

anti-fungals (for yeast), essential fatty acids, and enzymes for a

while (at least 4 months for most of those) because she is ASD, so they

may (likely) have contributed to our success using Natural Calm. From

memory, others on the Miralax group have used Vitamin C, Fruit-Eze,

PlumSmart juice (made by Sunsweet and in your grocery store), and

KidLax. I haven't used any of those so can't give you advice on them,

but I can say that others have reported great success. The Miralax

group has been as helpful to me as this Enzymes and Autism group. Good

luck and feel free to email me with more questions,

Carol

>

> I am brand new to this group. My son has been consitpated most of

his

> young life (he is 4 and a half now). He has been on and off Miralax,

> Kondremul, and senna drops. Nothing seems to help. I have been to

> two GI specialists. One told me it is a result of functional stool

> holding. Since they associate bowel movements with pain they tend to

> hold their stools in. This just aggravates the problams.

>

>

> I am ready to try anything.

>

>

>

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>

> I went through the same thing with both of my children. My son ended

up with encopresis (a leakage of stool and accidents due to muscle

damage). When he is constipated now, I give him Magnesium Citrate

which is a powder that you mix in water or juice. It tastes citrusy.

Also give Vitamin C every day (can give up to bowel tolerance). We

also made both my kids do their " 10 minutes " in which they sat on the

tiolet for that amount of time and read a book, hoping to train their

bowels. Don't have them push or anything straining, but sometimes just

the act of sitting in that position leads to going. Hope this helps.

Amy

>

>

> I am brand new to this group. My son has been consitpated most of

his

> young life (he is 4 and a half now).>

>

>

>

>

>

>

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Just wanted to jump in and say that we see a chiropractor also and it has

helped tremendously in terms of helping the immune system and also helping to

calm both of my children now ages 4 and 6. We started a couple of months before

my daughter turned 3 years old. Now we get adjusted once every 2 weeks.I would

highly recommend it based on my experience. :o)

Ginger

P.s. I started going soon after my children and found out that I had

scoliosis. It helps with that also. MHO </HTML>

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Hello,

For us, our saving grace was taking our son to see a holistic

chiropractor, that practices " Hole-In-One " method on cervical

spine. It is possible that your son has a pinched spinal cord and

this is causing his onset of behaviors. When pinched, it causes a

tightness in the brain, sensory issues are noted, quick tempers,

seizure-like staring behavior, slowed auditory processing... these

are all things I notice get better when my sons spinal is

straightened. Our kids bump and fall so often, a bad fall could

have caused a change in his spine. It happens alot with my 2 boys -

age 3 and 6.

Also, we do Cranial Sacral Therapy, with an excellent, experienced

therapist. This CST has helped my 6 year old no longer be

dysgraphic, because now he writes insead of staring off to the

ceiling. And my other son stopped his staring spells after seeing

both doctors.

You should learn more about the spine and what it means to be out of

line. Alot of these autistic symptoms are eased or go away upon

correction.

These are inexpensive alternates that cannot hurt to try. The chiro

is a $40 visit, and the CST is $25. Not much money for something,

that for us, has shown to be more effective and lasting then any

amount of Speech and OT that we've done. For anyone who'd like

further explanations about our experience, e-mail me. Also, I live

in Michigan.

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I would like more information on how to find a CSTherapist...I tried the

website that was offered a while back, but couldn't find anywhere on it to

locate a practitioner. If you have any info on finding a practitioner for

CST, please email me privately at quicksilvergirl75@.... This

address is bouncing emails, unfortunately. Thanks!

in CA

Wife of 9 years to Phil

Mother to Emma (8), Jack (6), baby Graham b/d 6-2-05, and Liam

(1 year)

Homeschooling for our 4th year

Our blog about our kids: http://philhalpin.com/blog/kidsstuff.html

" Be gentle to all, and stern with yourself.” --St. Theresa of Avila

Re: HELP!!!!

Hello,

For us, our saving grace was taking our son to see a holistic

chiropractor, that practices " Hole-In-One " method on cervical

spine. It is possible that your son has a pinched spinal cord and

this is causing his onset of behaviors. When pinched, it causes a

tightness in the brain, sensory issues are noted, quick tempers,

seizure-like staring behavior, slowed auditory processing... these

are all things I notice get better when my sons spinal is

straightened. Our kids bump and fall so often, a bad fall could

have caused a change in his spine. It happens alot with my 2 boys -

age 3 and 6.

Also, we do Cranial Sacral Therapy, with an excellent, experienced

therapist. This CST has helped my 6 year old no longer be

dysgraphic, because now he writes insead of staring off to the

ceiling. And my other son stopped his staring spells after seeing

both doctors.

You should learn more about the spine and what it means to be out of

line. Alot of these autistic symptoms are eased or go away upon

correction.

These are inexpensive alternates that cannot hurt to try. The chiro

is a $40 visit, and the CST is $25. Not much money for something,

that for us, has shown to be more effective and lasting then any

amount of Speech and OT that we've done. For anyone who'd like

further explanations about our experience, e-mail me. Also, I live

in Michigan.

__________ NOD32 2176 (20070410) Information __________

This message was checked by NOD32 antivirus system.

http://www.eset.com

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I don't know what

IYKWIM

is.

cathleen

chlobot wrote:

>

> My daughter was bitten about 7 weeks ago. We found the tick, engorged,

> after it had been

> attached for less than 24 hours. She developed a rash & we started her

> on 6 weeks of

> amoxicillan, which just ended.

>

> She developed a fever after starting the abx but has had no other

> obvious symptoms since.

> However, for the last week or so she's been very " high strung " . I'll

> admit outright that she's

> high strung anyhow but now the behavior is suspect, IYKWIM. She tends

> to get a bit

> irrational and tantrummy a bit mroe easily than usual. She's somewhat

> " demanding " and gets

> loud when things don't go her way. She also totally overreacts to

> things by whining, crying,

> etc. Yes, some of it could be being a 4 yr old but this seems extreme.

>

> Does it sound like she still has the lyme bug or maybe needs some

> detox from the chmicals.

> In addition to the abx we have been giving her Astragalus,

> andropgraphis & resveratrol,

> probiotics, cod liver oil and doing epson salt/hydrogen peroxide detox

> baths several times a

> week.

>

> What else can I do? I'm petrified that this might get out of hand.

>

>

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It's an acronym for If You Know What I Mean

cathleen rehfeld wrote:

>

> I don't know what

>

> IYKWIM

>

> is.

>

> cathleen

>

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There is a good chance she is still sick. Amoxicillin did absolutely

nothing for me. I ended up taking three rounds of IV antibiotics later, none

of it

cured me. The only thing that helps me somewhat is the Buhner herbs etc.

maybe you can follow up with herbal meds. Did you read the Buhner book? You

can tailor the herbs to the actual symptoms. if you have not read it yet I

would highly recommend it.

Dagmar

**************Get the scoop on last night's hottest shows and the live music

scene in your area - Check out TourTracker.com!

(http://www.tourtracker.com?NCID=aolmus00050000000112)

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Thanks for the help! I too have dificulties with " the lingo " at

times. =)

Thanks so much.

=)

Robynn

> >

> > I don't know what

> >

> > IYKWIM

> >

> > is.

> >

> > cathleen

> >

>

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Why did your doc prescribe amoxicillin? I though doxycycline is the

most widely prescribed/accepted treatment. I think I would ask for a

month of doxy to be conservative.

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Have you tried magnesium? A lot of at bedtime?

>

> i need this girl to sleep. she looks bad.

> someone suggested amino acid solution, along with coline bitartrate.

> suggestions please

>

> melatonin makes her violent, and chlonidin (sp???) doesnt work to well.

>

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Try ornithine that works naturally to help sleep. Take 4000mg 8 500mg

capsules. This is for ages 12+ younger decrease the amount by ½

Take care

wani

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Since clonidine didn't work, you probably won't use it again. But I

wanted to alert you to its side effects.

http://www.drugs.com/clonidine.html

>

> i need this girl to sleep. she looks bad.

> someone suggested amino acid solution, along with coline bitartrate.

> suggestions please

>

> melatonin makes her violent, and chlonidin (sp???) doesnt work to

well.

>

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Can someone plz help me understand these reading?I just had a cbc and i don't

understand a thing my greatest concern are the readings that are low, everything

else is normal. I've had four infections this year so i'm kinda concerned looks

like I may hv another.

WBC.....3.39

RBC.....10.6

HGB......31.1

neutrophils........70.4

lymphocytes........18.1

i've had congestion and a sore thraught for a few days now also

aliza yaffa

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