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Re: MRI results are in

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Ahhh phooey on the school!! whyyyyyy do they make everything so

difficult :(

Sara gets her medicine before school and then at night. Heehee I don't think

Sara's school would give me a hard time about her medicine, if she had to

take it at school. Ive been up there at lunch time and the line for medicine

goes out into the hallway.

Good news about the cyst, as Sara's DR told me " noooooo tumor " with a heavy

accent lol

Kathy mom to Sara 8

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, you may want to share a copy of the " flag pole " mom story with the

school. Ask them if they really want to have something like that happen at

their school... just a thought. Kim.

MRI results are in

Whew...finally got the report in yesterday.

does not have a cyst!! He has a small cerebellum (common for DS)

and

that would not cause the seizures. The cause of the seizure is UNKNOWN

(actually most are unknown).

He is tolerating the medicine well. I bought him colace for the

constipation

(his tummy was hard as a rock this afternoon). He refuses to take the

colace..hummmm...everything else he takes fine. The pharmacist did tell me

that the Bactrim would probably loosen up his stools...well tonight they

did!!

I am having a problem with the school and the medication. The rx says one

thing...I wrote down the instructions (we have to bump the dose up every

four

days) and faxed this memo to the school with a cc to the Dr. Meanwhile, I

send a copy of the medication form along with the memo (I put see Memo on

the

paper)...the Dr finally signs the form today and faxes it back. But the

school will not allow it because the doctor did not write down the exact

dosing. The Dr abbreviated it on paper when I was there (not on the rx

though) and I understood it. I even made a note on the fax to the doctor to

review and make sure I had it down. Sheesh!! Then yesterday, the nurse

said

they didn't think he needed the medication at school. He gets a dose at 6

am, one at 1:30 and the third one at 9:00 (bedtime). I told her, " what, I

am

suppose to quit my job so I can give him medication in the afternoon " .

GEESH!!!!!!!!!!!!! What is their problem????

I had bought a box of fancy cookies at Trader Joes and was going to take it

in to the school nurse. Not after that comment yesterday...I took them into

work instead, hehehe!! Tim and I are giving his medication at

school

for now....not sure how much longer we can do this.

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,

Stick to your guns. I had to take Willie's Prescription bottle into the nurse's

office and I asked the pharmasist for an extra the last time I had his Adderall

filled. Other wise I would be doing the same thing!

Hugs beth

" The right to be heard does not automatically include

the right to be taken seriously. "

- Hubert Humphrey

http://www.twinenterprises.com/trach/trachkids/kids2/br

ittany.htm

Beth(HMS) mom to beth 8(HMS), Brit 7

DS,tracheomalacia,asthma and

reflux/corrected), and Willie 6 who is onry only.

_________________________________________________________________

iVillage.com: Solutions for Your Life

Check out the most exciting women's community on the Web

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In a message dated 11/30/00 12:38:30 PM Eastern Standard Time,

Dawn.Shaw@... writes:

<< It's not for the school nurse to decide when he needs his medication!!!!!

>>

Of course you are right--it is not up to the school nurse to decided time of

delievery of a medication--however he/she is governed by laws that require

certain things. One is clear directions from the doctor that is attached to

the medication and many states also require a written permission from the

parent as well. S/he has to dot all her " i " s and cross all her " t " s. :)

nancy

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,

It's not for the school nurse to decide when he needs his medication!!!!!

Yikes, they drive you nuts huh? The Dr. makes that choice, not her.

Sorry, this just gets me that they think they can second guess a

prescription from a dr. and not just do their job!!!!!!!!!

Dawn (mom to 7ds)

I am having a problem with the school and the medication. The rx says one

thing...I wrote down the instructions (we have to bump the dose up every

four

days) and faxed this memo to the school with a cc to the Dr. Meanwhile, I

send a copy of the medication form along with the memo (I put see Memo on

the

paper)...the Dr finally signs the form today and faxes it back. But the

school will not allow it because the doctor did not write down the exact

dosing. The Dr abbreviated it on paper when I was there (not on the rx

though) and I understood it. I even made a note on the fax to the doctor to

review and make sure I had it down. Sheesh!! Then yesterday, the nurse

said

they didn't think he needed the medication at school. He gets a dose at 6

am, one at 1:30 and the third one at 9:00 (bedtime). I told her, " what, I

am

suppose to quit my job so I can give him medication in the afternoon " .

GEESH!!!!!!!!!!!!! What is their problem????

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  • 2 years later...
Guest guest

,

I'm glad you are going to have another opinion. It's always better when

surgery is suggested. My Mom had tennis elbow that wouldn't respond to any

treatment. Out of desperation, she tried acupuncture, and it was very

successful and has not returned. But my Mom doesn't have RA, so I'm not

sure if that makes a difference. It may be worth a try if it avoids

surgery.

Tennis Elbow (Lateral Epicondylitis)

Shock Wave Helps Tennis Elbow

http://content.health.msn.com/content/article/48/39175.htm

Acupuncture's Analgesic Effect on Tennis Elbow Pain

http://acupuncture.com/Research/Elbow.htm

Acupuncture for Tennis Elbow

Study Suggests Treatment Is Effective, Even in Difficult Cases

http://www.acupuncturetoday.com/archives2001/feb/02elbow.html

http://www.nlm.nih.gov/medlineplus/elbowinjuriesanddisorders.html

http://www.scoi.com/teniselb.htm

http://www.medinfo.co.uk/conditions/tenniselbow.html

http://www.intelihealth.com/IH/ihtIH/WSIHW000/9339/23813.html

a

> Hi, My doc. just called to say MRI showed ligament and tendon damage.

> At first he said he wanted to operate to do a nerve release. Now he

> says take out damaged parts and reattach good ligament and tendon to

> bone. 6 to 9 months recovery.

> Thats a little different.

> I am going for another opinion.

> Whitehouse,

>

>

>

>

>

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  • 1 year later...

-Hi Dick,

I'm sorry I can't remember your meds. They traced numbness and

tingling in my hands and feet to remicade. I know other meds cn case

neuropathy as well.

Hope you find an answer,

Marti

- In , " woodworkerdp "

<woodworkerdp@y...> wrote:

> The MRI results are back and I don't have a pinched nerve. It did

> show Osteoarthritis and joint deterioration which we already new

but

> not pinched nerve. So now it's back to the family doctor (internal

> medicine) to continue trying to find out what is causing the

> numbness in my arms, hands and fingers. I can't hold on to a

> magazine to read without my hands and arms going numb and I also

> drop a lot of things. It gets very discouraging.

>

> I have had the carpel tunnel test done and no carpel tunnel and now

> the MRI and no pinched nerve. Does anyone know what else could

> cause the numbness in the arms, hands and fingers? Any suggestions

> to take to the doctors would be appreciated. I do have swelling in

> the wrist from the arthritis but was told that wouldn't cause

> numbness.

>

> Thanks

>

> Dick

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I know when I had my first nerve conduction study that they only

tested from the forearm to the fingertips. If they applied

the " jolt " above the elbow and hooked the probes to your fingers,

then the elbow was included. In my second test, they had me fold my

arms at the elbow and wait several minutes. Even then, the signal

was only very slightly delayed. I do know that arthritis is

mentioned as a complicating factor in many of the articles you find

on the net about ulnar neuropathy. I also know how uncomfortable and

unsettling it is and I hope they get to the bottom of it soon! Good

luck, keep reading and asking questions. Steve

> > I have the same condition. I had a nerve conductivity test done

> which showed nerve pinching in the elbows - even though I have some

> pins and needles sensation above the elbow as well.

> >

> > Greg.

> > [ ] MRI Resluts Are In

> >

> >

> > The MRI results are back and I don't have a pinched nerve. It

> did

> > show Osteoarthritis and joint deterioration which we already

new

> but

> > not pinched nerve. So now it's back to the family doctor

> (internal

> > medicine) to continue trying to find out what is causing the

> > numbness in my arms, hands and fingers. I can't hold on to a

> > magazine to read without my hands and arms going numb and I

also

> > drop a lot of things. It gets very discouraging.

> >

> > I have had the carpel tunnel test done and no carpel tunnel and

> now

> > the MRI and no pinched nerve. Does anyone know what else could

> > cause the numbness in the arms, hands and fingers? Any

> suggestions

> > to take to the doctors would be appreciated. I do have

swelling

> in

> > the wrist from the arthritis but was told that wouldn't cause

> > numbness.

> >

> > Thanks

> >

> > Dick

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-

Hi Dick,

Here is a link that talks about nerves and different causes for the

problems with them. meds, RA, are mentioned...I know lipitor was one

of the listed meds that can cause it...I am taking zocor.

also...cancer meds...which could include MTX.maybe you could ask your

doc about holding one to see if your problem improves.

http://www.mayoclinic.com/invoke.cfm?objectid=299185F1-834D-4191-

9573A9B58C3D3D6B & dsection=3

it sure can et comlicated and discouraging!

Marti

-- In , " woodworkerdp "

<woodworkerdp@y...> wrote:

> Thank you everyone,

>

> This is a list of the meds I am now on. At the time the numbness

> started, about 4 years ago, I wasn't on any of these meds. As time

> has gone on, the numbness has gotten worse. As I noted, I can't

> even hold a magazine without my hands and arms going numb.

>

> I see the doctor in the morning and will mention about the elbow.

> Did x-rays show the condition, Or is there another test that needs

> to be done to the elbow? I thought the elbows were test when I

had

> the carpel tunnel test done. Is this a different test?

>

> Lipitor, 40 mg,

>

> Methotrexate, 2.5 mg, 5 a week

>

> Folic Acid, 400 mcg, 6 a day

>

> Diovan, 80/12.5,

>

> Nexium, 40 mg,

>

> Torsemide, 20 mg

>

> Potassium, 595 mg

>

> Temazepam, 15mg

>

> Enbrel, 25mg vial, injections twice a week

>

> Mobic, 7.5 mg, 1 - 2

>

> Ultracet, 0-M/650, 1 or 2 tablets 4 times a Day

>

> Hydrocodone/APAP 10/500 TABMCK,

>

> Foradil Aerolizer, 12mcg

>

> Pulmicort, 200mcg,

>

> Blephamide Opth. Susp, 10ml

>

> Singulair, 10 mg

>

> Alabutterol Inhaler

>

>

>

> Thanks for all your help.

>

>

>

> > I have the same condition. I had a nerve conductivity test done

> which showed nerve pinching in the elbows - even though I have some

> pins and needles sensation above the elbow as well.

> >

> > Greg.

> > [ ] MRI Resluts Are In

> >

> >

> > The MRI results are back and I don't have a pinched nerve. It

> did

> > show Osteoarthritis and joint deterioration which we already

new

> but

> > not pinched nerve. So now it's back to the family doctor

> (internal

> > medicine) to continue trying to find out what is causing the

> > numbness in my arms, hands and fingers. I can't hold on to a

> > magazine to read without my hands and arms going numb and I

also

> > drop a lot of things. It gets very discouraging.

> >

> > I have had the carpel tunnel test done and no carpel tunnel and

> now

> > the MRI and no pinched nerve. Does anyone know what else could

> > cause the numbness in the arms, hands and fingers? Any

> suggestions

> > to take to the doctors would be appreciated. I do have

swelling

> in

> > the wrist from the arthritis but was told that wouldn't cause

> > numbness.

> >

> > Thanks

> >

> > Dick

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  • 1 year later...

louise,

So happy to hear that this was something simple and treatable. This diagnosis

certainly makes sense. We all have a tendancy to think the worse, especially

with our children.

Jackie

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louise,

So relieved to hear the results. Now you know what to expect if she has another

sinus infection. I'm surprised she never spiked a fever.

My soon to be 3 year old with CMT has also had sinus problems. After a course

of antibiotics and contstant post nasal drip and cough, My pediatrician called

with his MRI results ( which was done for his nuero workup before his CMT

diagnosis) showing inus inflamation and asked if he was symptomatic...yes like

I've been trying to tell you. Although he was only 18 months at the time I can

imagine he too had a headache.

I am right there with you. The constant worring about their health. The latest

with has been a persistant hives lasting 5 weeks with no relieve from

Zertec. We finnally saw an alllergist since he also has asthma. It is not a

allergic reaction but possibly a histamine reaction to a virus he might have had

7 weeks ago or a disease process manifesting as a rash and will need further

blood test if he doesn't respond to a 2 week course of Zertec.

So of course I too think of the worst and fear the possibility of putting him

through more blood test. He has had at least 6 different blood draws for gentic

testing and the ruling out process.

Take Care

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HI, Louise

I am so happy to hear the MRI results.

I am sorry Katelyn has an infection but happy that is all it is. My kids

have really scared me only to find out it was nothing. What a great feeling

" Nothing " is ..

I hope we can help you in the future.

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