Jump to content
RemedySpot.com

medication

Rate this topic


Guest guest

Recommended Posts

I can't recommend any, but I trust you'll do your homework before ordering.... You really have to be careful of allot of the pharmacies outside of the US. The laws are different and the strengths can be measured differently. Not to mention they are not monitored by the FDA.

Medication

Can anybody recommend a Canadian online pharmacy?Please visit the Zapper homepage athttp://www.ZapLife.org

Link to comment
Share on other sites

Try emailing bruce@.... Bruce Greenberg spoke

to a group of senior citizens at California State University, Long Beach,

about buying drugs from Canada. He assured everyone that the meds were the

same as those issued by U.S. pharmacies. You can email him for particulars

including prices. Some drugs are not available and he'll let you know which

ones.

I have NOT personally used his service and therefore CANNOT VOUCH for him.

Several seniors in the group did order drugs through his company and were

very satisfied. He warned everyone not to trust Mexican pharmacies because

of counterfeit drugs being marketed there. His assurance of Canadian

pharmacies is because of Canada's similar pharmaceutical laws. The way it

works is that your physician writes a prescription which Bruce's company

forwards to Canada. A Canadian physician has to rewrite the prescription

since they do not fill American prescriptions. The pharmacy then ships the

drugs directly to the patient. At least that's what he said. I asked about

the legality of this business and he said that was an unresolved issue.

U.S. pharmaceuticals are pressuring the Congress to stop foreign

prescriptions. It means a huge loss of income to them. We pay the most for

prescription drugs. Pharmaceutical companies say it is to cover the cost of

R & D but they fail to mention that the government grants millions of dollars

for research. We, the taxpayers, foot that bill. Believe me, pharmaceutical

companies are making money hand over fist.

Mike

> [Original Message]

> From: prelda <prelda@...>

> < >

> Date: 8/22/2004 4:41:18 PM

> Subject: Medication

>

> Can anybody recommend a Canadian online pharmacy?

>

>

>

>

> Please visit the Zapper homepage at

> http://www.ZapLife.org

>

Link to comment
Share on other sites

> > Pharmaceutical companies say it is to cover the cost of

> R & D

You know, I've always wondered why we Americans are supposedly

footing the entire R & D bill. If it were true that that's why they

cost so much, shouldn't the same drug cost the same amount in Canada

too???

Bridget

Link to comment
Share on other sites

Other countries have price controls on the drugsBridget <rumplegroups@...> wrote:

> > Pharmaceutical companies say it is to cover the cost of> R & D You know, I've always wondered why we Americans are supposedly footing the entire R & D bill. If it were true that that's why they cost so much, shouldn't the same drug cost the same amount in Canada too??? BridgetPlease visit the Zapper homepage athttp://www.ZapLife.org

Link to comment
Share on other sites

I believe Canada has price controls.

> [Original Message]

> From: Bridget <rumplegroups@...>

> < >

> Date: 8/23/2004 7:39:14 AM

> Subject: Re: Medication

>

>

> > > Pharmaceutical companies say it is to cover the cost of

> > R & D

>

> You know, I've always wondered why we Americans are supposedly

> footing the entire R & D bill. If it were true that that's why they

> cost so much, shouldn't the same drug cost the same amount in Canada

> too???

>

> Bridget

>

>

>

>

>

>

> Please visit the Zapper homepage at

> http://www.ZapLife.org

>

Link to comment
Share on other sites

  • 2 months later...

My dd has been on a few different meds. With her, it seemed that they had the opposite effect of what they were designed to do. Each child is different, however, remember that our kids chemical balance in the brain is much different than the norm. I do have friends who've put their kids on meds and they can see tons of differences, some of these kids have been through the "guinea pig" med game in order to find one that works for them.

It all depends on what your family is ready to dive into. I would question a teacher that recommends meds. Teachers in my area that recommend meds, usually do so to make their jobs easier, it's not for the benefit of the child.

Karyn, Mom to 4.10 yoa, dx'd severely autistic, hypotonia, APD, GF/CF, SCD 10 mths

"I hope that there is a special place in Heaven for any child who's life on Earth was Hell, and a special place in Hell for those who made it so!!" K. Blanco

Medication

My 6 year old grandson has been diagnosed on the autism spectrum (probably asperger but currently PDD). His teacher is indicating she thinks medication will help. My daughter is opposed. Is anyone's child on medication such as adderall or concertra and if so, do you notice any difference? The main thing the teacher is hoping the medication will do is calm him enough to be able to participate in the therapy sessions. Not that the medication is a cure but a help.What are your thoughts?Becky

Link to comment
Share on other sites

My son was on Focalin and Ritalin and both had negative effects. My son started to have these emotional meltdowns. Meltdowns would usually occur maybe once in a few months, but he was having them everyday after being on them about 3 days. But every child is very different and I have heard just as manny success stories as well. I will say this much, a teacher really should not be suggesting that a student be put on medication. I work in the school system and that is frowned upon. Now a teacher could suggest to the parents to seek the opinion of a doctor, but not to out right say "Your child needs to be on medication." To say a child needs to be on medication is to say that they have been diagnosed with as condition that requires it. And a teacher cannot "diagnose" a child. Seek outside "medical opinion" and don't rely on what your teacher's opinion is to be the end-to-all for your child.

HEard Karyn <klmitch@...> wrote:

My dd has been on a few different meds. With her, it seemed that they had the opposite effect of what they were designed to do. Each child is different, however, remember that our kids chemical balance in the brain is much different than the norm. I do have friends who've put their kids on meds and they can see tons of differences, some of these kids have been through the "guinea pig" med game in order to find one that works for them.

It all depends on what your family is ready to dive into. I would question a teacher that recommends meds. Teachers in my area that recommend meds, usually do so to make their jobs easier, it's not for the benefit of the child.

Karyn, Mom to 4.10 yoa, dx'd severely autistic, hypotonia, APD, GF/CF, SCD 10 mths

"I hope that there is a special place in Heaven for any child who's life on Earth was Hell, and a special place in Hell for those who made it so!!" K. Blanco

Medication

My 6 year old grandson has been diagnosed on the autism spectrum (probably asperger but currently PDD). His teacher is indicating she thinks medication will help. My daughter is opposed. Is anyone's child on medication such as adderall or concertra and if so, do you notice any difference? The main thing the teacher is hoping the medication will do is calm him enough to be able to participate in the therapy sessions. Not that the medication is a cure but a help.What are your thoughts?Becky__________________________________________________

Link to comment
Share on other sites

My eight year-old has been on several medications over the years and

for the past two years has been on a good mix of risperdal,

trileptal and concerta. We recently increased the concerta and had

the problems with the meltdowns but when we dialed the dosage back a

little they disappeared. Apparently many of our kids can get by with

a much lower dosage than the general population.

While it is true that teachers often seem to push medications more

than others, I have to say that we have been VERY happy with the

results that we have gotten, and I was VERY opposed to them at

first. I finally changed my mind when I was pregnant with my 4 year-

old and I was worried about my safety with a child who was

constantly having explosive meltdowns. It was difficult to find the

right meds and the right dosage, but it has made all the difference

in Nico's life and in our family's life. Of course, I hope he will

be able to come off of some, if not all, of them one day, but in the

mean time I am thankful that we have no serious side effects and

that our current meds have not lost their effectiveness.

Stacey

> My dd has been on a few different meds. With her, it seemed that

they had the opposite effect of what they were designed to do. Each

child is different, however, remember that our kids chemical balance

in the brain is much different than the norm. I do have friends

who've put their kids on meds and they can see tons of differences,

some of these kids have been through the " guinea pig " med game in

order to find one that works for them.

>

> It all depends on what your family is ready to dive into. I would

question a teacher that recommends meds. Teachers in my area that

recommend meds, usually do so to make their jobs easier, it's not

for the benefit of the child.

>

> Karyn, Mom to 4.10 yoa, dx'd severely autistic, hypotonia,

APD, GF/CF, SCD 10 mths

>

> " I hope that there is a special place in Heaven for any child

who's life on Earth was Hell, and

> a special place in Hell for those who made it so!! " K. Blanco

> Medication

>

>

>

> My 6 year old grandson has been diagnosed on the autism spectrum

> (probably asperger but currently PDD). His teacher is indicating

> she thinks medication will help. My daughter is opposed. Is

> anyone's child on medication such as adderall or concertra and if

> so, do you notice any difference? The main thing the teacher is

> hoping the medication will do is calm him enough to be able to

> participate in the therapy sessions. Not that the medication is a

> cure but a help.

> What are your thoughts?

> Becky

>

>

>

>

>

>

Link to comment
Share on other sites

With some children on the autism spectrum, it's not a question of

whether they can pay attention, but a question of tuning into their

special interests. Many can pay attention for literally hours if the

teacher or parent connects through whatever is driving the child's

interest at the moment. I remember a few years ago hearing about

teaching math by dividing Pokemon cards, for instance.

It's also possible that some kinds of movement could be allowed " while "

the child is concentrating. My daughter always jiggled her left knee

-- really hard and annoyingly -- when she was concentrating. She's

working on a master's degree now, and she still jiggles away while she

is working on her assignments. Movements like this are referred to as

" stims " , and serve a purpose for people who can't just sit still and

concentrate on demand.

Patty

rfholcom wrote:

> My 6 year old grandson has been diagnosed on the autism spectrum

> (probably asperger but currently PDD). His teacher is indicating

> she thinks medication will help. My daughter is opposed. Is

> anyone's child on medication such as adderall or concertra and if

> so, do you notice any difference? The main thing the teacher is

> hoping the medication will do is calm him enough to be able to

> participate in the therapy sessions. Not that the medication is a

> cure but a help.

> What are your thoughts?

> Becky

Link to comment
Share on other sites

If you go to the following link, you will find a report compiled by

the Autism Research Institute on biomedical interventions for

children with autism. The report is based on parent observation.

ARI has been around for years and has enough parents available to

collect what i consider to be significant data. I would like to

say, though, that as someone who has been doing this for awhile now,

you will see chelation as remarkably effective. It may be, but it

is also as popular right now as secretin is. I was around during

the secretin discovery, tried it, and yes i saw results. But, I

realize that sometimes we need to see results, and that new " cures "

will often be seen as effective in the beginning. Chelation has

been around a long time, and does work for what it is designed for,

of course. I'm even willing to try it, almost. The anti-fungals on

the list also show quite a bit of effectiveness, and i do believe

that they work. I do not, however, think that we know how to use

them to effectively treat candida yeast. We did nystatin a little

over a year ago. It was an every day dose. It did help dd, but the

longer she was on it, the more bad behaviors. To me, this indicates

that by the very nature of what nystatin does, it can be overdone,

as easily as underdone. Our bodies are supposed to have some things

in them, and i think candida yeast serves a purpose, but when an

overgrowth occurs, it harms some kids. On the other side of that

coin it makes sense that if the candida yeast was completely killed

off, perhaps there is something else that becomes overabundant

because the candida yeast is no longer available for it's purpose.

Medications are something we waited until after the age of 6 for,

except for secretin...i was caught up in the " cure " aspect, and did

it anyway. I've developed the opinion that even that " cure " must be

administered differently if it is to be used over time, because a

big push of a drug one time is not the same as correcting the

missing agent's avaiability in the body long term. I personally

hoped that the use of the secretin cream would show results larger

that it has, but there again, even though it is able to be released

slowly and transdermally, it is not the same as making it available

in the organ it was meant to occur in. We've used some various

medications, but dd reacts badly to most. I dont even consider it

to be just a reaction to the medicines, but maybe some of the

fillers that make medication deliverable in the body, because i have

trouble with some meds as well, and the only common denominator

would have to be the fillers, or dyes, because the active ingredient

varies. A tip on meds. NEVER get a full prescription! I've lost

lots of money on meds that no one could even take after the first 7

days! Anyway, here's the link i told you about an hour

ago***blushing***:

http://www.autism.com/ari/specialinterest/form34q.html

Link to comment
Share on other sites

Hi Becky,

We had a success with Adderall. My child was in danger of losing his

inclusion placement at about the age your grandson is, so we decided to

give it a try and it worked. He improved in all areas. We found a

good match pretty quickly but have since tried to switch to extended

release version of Adderall and Concerta and it was very bad. Also,

the generic of Adderall was very, very bad for him. I have since heard

that a lot of kids don't do well with extended release meds. So, if

they decide he really needs it, don't give up after the first try.

Now, I am trying some biomed stuff to help him be able to do without it

someday. We have not had to raise his dosage for a long time so I'm

thinking maturation may be helping some, too. Good luck with the

decision.

On Nov 13, 2004, at 11:21 AM, rfholcom wrote:

>

>

> My 6 year old grandson has been diagnosed on the autism spectrum

> (probably asperger but currently PDD). His teacher is indicating

> she thinks medication will help. My daughter is opposed. Is

> anyone's child on medication such as adderall or concertra and if

> so, do you notice any difference? The main thing the teacher is

> hoping the medication will do is calm him enough to be able to

> participate in the therapy sessions. Not that the medication is a

> cure but a help.

> What are your thoughts?

> Becky

>

>

>

>

>

>

>

>

Link to comment
Share on other sites

>As a nurse and a lawyer, i think it is outrageous for a teacher to suggest

such a thing. First off, concerta and ritalin, etc., does not typically help

these children but can make things worse. (i know i have tried them for my

autistic daughter since my adhd sone was on them). I still cannot believe the

teacher suggested this.

terry poling

> From: " rfholcom " <kholcomb@...>

> Date: 2004/11/13 Sat PM 04:21:43 GMT

> autism

> Subject: Medication

>

>

>

> My 6 year old grandson has been diagnosed on the autism spectrum

> (probably asperger but currently PDD). His teacher is indicating

> she thinks medication will help. My daughter is opposed. Is

> anyone's child on medication such as adderall or concertra and if

> so, do you notice any difference? The main thing the teacher is

> hoping the medication will do is calm him enough to be able to

> participate in the therapy sessions. Not that the medication is a

> cure but a help.

> What are your thoughts?

> Becky

>

>

>

>

>

>

>

>

Link to comment
Share on other sites

Owen's teacher suggested meds, too. He's not even 4 yet.

In a message dated 11/15/2004 9:19:54 PM Eastern Standard Time, autism writes:

Message: 6 Date: Mon, 15 Nov 2004 18:31:29 +0000 From: <terrypoling@...>Subject: Re: Medication>As a nurse and a lawyer, i think it is outrageous for a teacher to suggest such a thing. First off, concerta and ritalin, etc., does not typically help these children but can make things worse. (i know i have tried them for my autistic daughter since my adhd sone was on them). I still cannot believe the teacher suggested this.

Link to comment
Share on other sites

My daughter's DDK teacher suggested meds too. We have since switched her to another school and teacher.

Re: Medication>As a nurse and a lawyer, i think it is outrageous for a teacher to suggest such a thing. First off, concerta and ritalin, etc., does not typically help these children but can make things worse. (i know i have tried them for my autistic daughter since my adhd sone was on them). I still cannot believe the teacher suggested this.

Link to comment
Share on other sites

I am new to the group and wanted to share a little about myself before replying. I have a 19 yr old child with special needs. He does not have Autism, however I have worked with children in the spectrum since early 1997( In the public and private school setting as well as in the home.) My first question would be is the school staff meeting the child's sensory needs? It has been my experience that meds are the first thing to pop up in the teachers heads, without thinking about the individual child and their unique needs. 99% of the children that I have worked with are seeking to have their sensory needs met and once their sensory needs are being met the child will be able to focus and stay in his or her seat and remain on task. (A Sensory Diet) I have also found that meds such as adderall tend to have the adverse effect on children with Autism. I would only consider meds as an absolute last resort. As for the teacher suggesting meds- they were way out of line. They are supposed to be there to educate our children not diagnose and medicate.

Re: Medication>As a nurse and a lawyer, i think it is outrageous for a teacher to suggest such a thing. First off, concerta and ritalin, etc., does not typically help these children but can make things worse. (i know i have tried them for my autistic daughter since my adhd sone was on them). I still cannot believe the teacher suggested this.

Link to comment
Share on other sites

Teachers are not supposed to recommend meds- ever.

Concerning Adderall ( standard not time-release), my son does very well with it. Of course, he is on a very low dose, as most SN kids are poor metabolizers of medications, and also cannot handle any type of time-release medication either

..

-Camden.

I have also found that meds such as adderall tend to have the adverse effect on children with Autism. I would only consider meds as an absolute last resort. As for the teacher suggesting meds- they were way out of line. They are supposed to be there to educate our children not diagnose and medicate.

Link to comment
Share on other sites

  • 2 months later...

--- In achalasia , " " <techangel1972@y...>

Hi - I have not taken Levsin but I just for the first time

took NuLev - in tablet form that you allow to disolve on your tongue.

I've only taken it twice and only half a tablet each time. I found it

made me slightly 'foggy' and tired but that's it. The spasm went away

after about 5 min or so and I was able to function for the rest of my

day. Once I have my baby and I'm done nursing - I wouldn't hesitate

to even take a full tab. The side effects were minimal compared to

other meds I've tried and I felt it was very effective.

Good Luck

Happy Swallowing!

in Va.

>

> Hi all. I have a question. Right now I am taking Ametryptaline (low

> dose antidepressent) for my spasms. It doesn't seem to be working

> much anymore. I have Levsin drops that I've never taken due to the

> fact of all the crappy side effects. Does anyone else take Levsin?

> Does it work? What side effects do you have? I swear my spasms have

> been getting worse....Its driving me nuts!!!!!!

> And if not Levsin, what about something else? Any suggestions from

> anyone? That way I can bring it up to my doctor and see if he can

> get me a prescription for something else. And I simply can't

swallow

> pills. So it must be in liquid form or tablets that I am able to

> crush. Any suggestions would greatly be appreciated. Thank you.

>

>

Link to comment
Share on other sites

  • 2 weeks later...

Zoloft. 25mg daily

She also takes digestive enzymes, (non rx)

which help immensely. (She was diagnosed with Encopresis a few years ago).

~Penny ~

JAX Management, Inc.

http://www.jaxmgt.com

Furthering the cause of

Autism Awareness

From: Carlson

[mailto:cathykay@...]

Sent: Sunday, February 20, 2005

4:35 PM

AutismBehavior

Subject: Medication

>Since she's been on medication, she's been able to go to school

without fear

and live a more independent life.<

Would you mind sharing what medication she is on? I

would appreciate it.

Link to comment
Share on other sites

  • 4 months later...
Guest guest

My daughter was put on Risperdal 0.25mg but we had to stop because it caused

her hands to swell and itch real bad! She also has asthma and I noticed her

needing her inhaler more often but once we stopped the meds it has cleared up.

I also dont like the idea that it can cause " lactating " these girls have

enough issues!!

Shirley

Link to comment
Share on other sites

Guest guest

Tara:

My son was on .25 mg of Risperdal and it helped him greatly, I wish we were

still on it sometimes! It helped a lot with his anger regarding his anxiety,

helped him get to sleep at night, it just helped. As for the other, maybe

someone else can give you information on that one.

Link to comment
Share on other sites

Guest guest

Hi, Tara. I have two daughters with OCD and have it myself. My youngest

one, , was diagnosed at seven and two years later my oldest one, Hannah,

was

diagnosed at eleven. has been taking Risperdal for about three years

now and it has helped her to be more calm than she is without it. She just

recently went from a dose of .25 to .5 a day. In addition to the Risperdal, she

also takes Luvox for the OCD and Clonidine to help her to fall asleep at

night. My other daughter takes Luvox and Abilify. I have no experience with

the

other med you asked about. Kelley in NV

Link to comment
Share on other sites

Guest guest

Kelley

Is it possible for you to tell me how it affects you now-the ocd. It gets

me so discouraged at times that my ds will have this forever. I just need

to know and hear from ppl who have " lived through it " and can function.

When the days are good it is so wonderful but times when it is raging seems

just so hopeless. Thanks:)

Lynne

From: kelleydinkins@...

Reply-

Subject: Re: Medication

Date: Thu, 7 Jul 2005 09:13:16 EDT

Hi, Tara. I have two daughters with OCD and have it myself. My youngest

one, , was diagnosed at seven and two years later my oldest one,

Hannah, was

diagnosed at eleven. has been taking Risperdal for about three years

now and it has helped her to be more calm than she is without it. She just

recently went from a dose of .25 to .5 a day. In addition to the Risperdal,

she

also takes Luvox for the OCD and Clonidine to help her to fall asleep at

night. My other daughter takes Luvox and Abilify. I have no experience

with the

other med you asked about. Kelley in NV

Link to comment
Share on other sites

  • 2 months later...

I have....Ms. Debbie ( the nurse) told me to ask Dr. Rutledge.....I have

e-mailed him about this several times but he has not e-mailed me back. I am just

so afraid of making CLOS mad.....

Thanks though.

Sincerely,

luv2gab2@... wrote:

Hi , call clos. That's the only way to make sure. They are there for

you.

Suzanne H.

Dr. R 7-17-03

High Point

270-170

Link to comment
Share on other sites

Hi ... have you ever called Dr. Rutledge? I know he supervised your

surgery with Dr. , I think you said, so he is the most likely person to

follow you. You can also ask Debbie P. to track Dr. R. down if you're having

trouble. I copy Debbie P. when I email my doc, so she knows where I'm at all

the time. Keep on top of it! hugs Kim

Knippers <prayerwarrior02@...> wrote:I have....Ms. Debbie ( the

nurse) told me to ask Dr. Rutledge.....I have e-mailed him about this several

times but he has not e-mailed me back. I am just so afraid of making CLOS

mad.....

Thanks though.

Sincerely,

luv2gab2@... wrote:

Hi , call clos. That's the only way to make sure. They are there for

you.

Suzanne H.

Dr. R 7-17-03

High Point

270-170

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...