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Re: other alternatives

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Have you considered that you may be able to stop the other meds if you

followed your RD's advice and went on Enbrel? Most people experience very

few side effects compared to MTX. I was able to stop all other meds

including pain meds when I went on Enbrel and I was on everything you are

taking except the tolectin. If you are concerned with Enbrel, read the

insert for MTX, especially the consequences of long term use. Enbrel may be

a more sensible choice if it works for you. Also, if you keep taking that

cocktail you may conceder taking folic acid supplements.

[ ] other alternatives

I was wondering if anyone on the list has tried other alternatives

than the usual meds for PA. At my last dr visit it was suggested

that I go on Enbrel. And while I know there are many people who are

thrilled with the drug...I have too many concerns and I just don't

want to go on it. I am currently on azulfidine,tolectin,and

methotrexate. I recently had a stomach bug and couldn't eat for

three days so I also didn't take my meds. I was amazed at how much

better I felt being off of everything. Not that my PA symptoms went

away but I have been less achy than I have been lately. So I begin

to think about alternative therapies but I have found little on the

net. Does anyone have any ideas they could point in my direction?? thanks

Tami

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I'd have to agree on that about the MTX...actually all of it is

frightening to mebut I ave always HATED taking any kind of medication

and now I'm on about 8. But I got the impression that the majority of

people are on ALL the same meds PLUS the Enbrel. If I am wrong then

that is great. I feel like I just keep adding. And also yes I'm

taking the folic acid too. I just forgot to mention it. Also, a blood

pressure med. One reason I am waiting on the Enbrel is cos I don't

know how much I'll have to pay myself and not sure I can afford it. I

carry my own insurance as I am self-employed.

thanks for the info

Tami

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  • 6 months later...
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Queen...I think you will find most of us have had the same

experience as you and have searched for other treatments along the

way. We each have found what works for us by experiments, being our

own health advocates, and trial and error. Don't give up. One thing

I will recommend is reading books on chronic illness and how to

accept the challenges and making the best of life. Read up in the

library on this site what we have tried and found also. I think

said it once...remember 50% of doctors graduated at the bottom

of their class and they don't know everything so question and search

til you find what works for you. Everytime I hear I need more

surgery (5 in 3 years now) I spend a day feeling sorry for me and

then get on with it. I have had this for 23 years and found

acceptance to be the key for me. Trudy.

> I've just had my 6th sinus polypectomy. I can't take it anymore.

Are

> there any other alternatives? herbal? Diet change? Etc? HELP!!!

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Thanx Trudy.

It helps to know I'm not alone in this. I read somewhere that

nutrients magnesium, B6, and zinc are helpful. It seems I'm having a

surgery almost every couple of years. You're right, I will keep doing

research, there's gotta be something...

>

>

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I second Trudy's thoughts. Its a process, and no one answer seems to

work for everyone, or even for anyone continuously over time. I've

benefited from finding the right meds, a sinus surgery, and diet

changes. I tried aspirin desens but can't maintain without side

effects.

It may be the diet changes have been the most subtle, yet profound

in impact. Although I avoid some of the worst salicylate foods, I'm

more dedicated to trying to eat more from " whole foods " concepts

popular with naturopaths, along with a few supplements. (I found

magnesium helpful when I started having heart palpitations and joint

pain last year).

One day at a time, one nostril at a time..

Alice

> Thanx Trudy.

>

> It helps to know I'm not alone in this. I read somewhere that

> nutrients magnesium, B6, and zinc are helpful. It seems I'm

having a

> surgery almost every couple of years. You're right, I will keep

doing

> research, there's gotta be something...

> >

> >

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Guest guest

I am a fellow person looking for alternatives. What I find so

frustrating that this doesn't seem to be as 'rare' as I am led to

believe. If this is the case, why? how etc? All the sites I have

looked at so far seem to look at just treating the individual

symptoms etc, what about the whole package?! My husband at one

stage found some interesting stuff, but it looks like noone is

really looking at that angle!

I am willing to try anything these days!

> > Thanx Trudy.

> >

> > It helps to know I'm not alone in this. I read somewhere that

> > nutrients magnesium, B6, and zinc are helpful. It seems I'm

> having a

> > surgery almost every couple of years. You're right, I will keep

> doing

> > research, there's gotta be something...

> > >

> > >

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  • 3 years later...
Guest guest

Have you ever tried antineoplastins, LimuPlus, or Ambrotose? Or has

anyone out there?

>

>

> Well, as a person LDN for almost 6 months, I can tell you a couple of

> things. Only problem for me was a major sleep disturbance for the

first

> week. Have had a couple of small symptom improvements

> which is a plus. Have never done steriods, but do quite a few

alternatives

> over my 20yr plus MS quest.

>

> Lorna

>

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