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Dear Ian,

I can only imagine how disconcerting it must be to have these tremors. I

agree that you should have them checked out by a doctor. Is there a chance

you are undernourished? I ask only because I read somewhere (can't remember

where) that anorexia is a possible side effect of IgAN or HSP. Sorry I can't

remember which of the two it was connected to. I know that I have had

trouble forcing myself to eat at times as has, and that might be a

contributor. As and other said, we are here to support you!

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Dear Ian

I am so very sorry to hear of your problem at the moment. I think the

shaky vibrations are not connected to IGAN. Are you on any medications

at the moment Ian that could be giving you side effects? Are you eating

well, I ask as having had eating problems myself, I used to shake badly

when hungry. I know it is very worrying for you and your girlfriend,

but please do get yourself checked out. We are here for support in

between time.

Best wishes

please help me

Hi guys,

Starting to get concerned with the vibrations in my body, very slight

but have started to increase throughout. My girlfriend has felt the

vibrations which are not visible. However, I apparently have a shaky

head!?! This causing her to panic and think it could be early stages of

'Parkinson's.

Am I the only person to be suffering with this?

Or is it a 'IgAN' symptom?

Any advice would much appreciated.

Many thanks

Ian

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Hi Ian.

I've also never heard of this as a symptom of IgAN. I don't recal your

kidney function situation, but a tingling-like feeling can happen if you

have really advanced kidney failure due to electrolytes imbalances. What

you're describing sounds a bit like it might be a tremor. You should have

that checked out by a doctor.

Pierre

RE: please help me

> Dear Ian

>

>

>

> I am so very sorry to hear of your problem at the moment. I think the

> shaky vibrations are not connected to IGAN. Are you on any medications

> at the moment Ian that could be giving you side effects? Are you eating

> well, I ask as having had eating problems myself, I used to shake badly

> when hungry. I know it is very worrying for you and your girlfriend,

> but please do get yourself checked out. We are here for support in

> between time.

>

>

>

> Best wishes

>

>

>

>

>

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Hi Ian,

If I recall correctly, when I was on predinsone my hands were shaking

tremendously... I've always been told I've had minor shake in my hands (nothing

that I've noticed personally, but other people have told me of it) and I believe

my neph told me predinsone can bring that out even more.

please help me

Hi guys,

Starting to get concerned with the vibrations in my body, very slight

but have started to increase throughout. My girlfriend has felt the

vibrations which are not visible. However, I apparently have a shaky

head!?! This causing her to panic and think it could be early stages of

'Parkinson's.

Am I the only person to be suffering with this?

Or is it a 'IgAN' symptom?

Any advice would much appreciated.

Many thanks

Ian

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No you aren't the only one Ian I had this and extreme shakes and body

jerks.......usually came on after something stressful, when my Neph saw me

with my head shakes he said that could be stopped and he put me on a small

dose of Atenalol which is a beta bloka. It worked and it happens very mildly

occassionaly but nothing as embarrassing or distressing as before.

I was told it was unlikely that it was Parkinson's but it looks just like

it, I know.

Best wishes

Sally.

please help me

Hi guys,

Starting to get concerned with the vibrations in my body, very slight but

have started to increase throughout. My girlfriend has felt the vibrations

which are not visible. However, I apparently have a shaky head!?! This

causing her to panic and think it could be early stages of 'Parkinson's.

Am I the only person to be suffering with this?

Or is it a 'IgAN' symptom?

Any advice would much appreciated.

Many thanks

Ian

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mentioned Prednisone as a potential for the shakes. I have to

agree with him completely.

I was only on Prednisone for a couple of months right after

diagnosis, and I shook so bad, I had to grab my arms to make them

stop sometimes. Just shaking someones hand was enough for me to

display Parkinson's -like symptoms.

As soon as I stopped taking Prednisone, the shaking stopped, and has

never returned.

Keep in mind that that I also had severe allergic reactions to

Prednisone, which eventually erupted into ulcers -- I would talk to

your doctor about this immediately.

Walt

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Hi Pierre, your response to Ians problem caught my eye. Im currently

scheduled for an EMG on my left foot because of tingling and numbness.You

mentioned electrolyte imbalance,could that be remedied by a

multi -vitamin.The tingling has been going on for a couple months.My doc

thinks it's from a pinched nerve.I disagree,I've been on disabilty and CPP

for the past 3 years because of IGAN and pulmonaty renal syndrome.I haven't

done anything physical enough to pinch a nerve.Gotta go, kitchens a mess and

the wife will be home soon from work.Don't want her to think I've been on

the computer all day :) Take care

RE: please help me

>

>

> > Dear Ian

> >

> >

> >

> > I am so very sorry to hear of your problem at the moment. I think the

> > shaky vibrations are not connected to IGAN. Are you on any medications

> > at the moment Ian that could be giving you side effects? Are you eating

> > well, I ask as having had eating problems myself, I used to shake badly

> > when hungry. I know it is very worrying for you and your girlfriend,

> > but please do get yourself checked out. We are here for support in

> > between time.

> >

> >

> >

> > Best wishes

> >

> >

> >

> >

> >

>

>

> To edit your settings for the group, go to our Yahoo Group

> home page:

> http://groups.yahoo.com/group/iga-nephropathy/

> Visit our companion website at www.igan.ca

>

>

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Hi .

No, a multi-vitamin won't affect an real electrolyte imbalance. I just

mentioned that as an example of what can cause tingling. Tingling and

numbness among kidney patients can also be caused by malnutrition and

vitamin B deficiency, and many kidney patients have what they call

peripheral neuropathy (affects mainly diabetics, I think), which also

manifests itself as tingling and numbness in the extremities. The first few

weeks on dialysis, they mentioned neuropathy a few times when I had tingling

after dialyis, until they finally figured out my calcium was too low (that's

an electrolyte). I had been just borderline, and when they put me on

dialysis, it dipped too low.

Kitchen is Ok here, so I'm just going to leave the snow for my wife to

shovel when she gets home, so she has something to do : )

Pierre

Re: please help me

> Hi Pierre, your response to Ians problem caught my eye. Im currently

> scheduled for an EMG on my left foot because of tingling and numbness.You

> mentioned electrolyte imbalance,could that be remedied by a

> multi -vitamin.The tingling has been going on for a couple months.My doc

> thinks it's from a pinched nerve.I disagree,I've been on disabilty and CPP

> for the past 3 years because of IGAN and pulmonaty renal syndrome.I

haven't

> done anything physical enough to pinch a nerve.Gotta go, kitchens a mess

and

> the wife will be home soon from work.Don't want her to think I've been on

> the computer all day :) Take care

>

>

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Ian,

I don¹t know where you are regarding kidney function, but my son had

pronounced tremors in his hands mainly when he tried to do some fine motor

task, like tie his shoes, dial the phone, etc. The tremors developed about 6

months before his transplant and he had to have a neurological consult

before the transplant to determine the cause. The neurologist decided they

were caused by the level of toxicity in his blood due to his low kidney

function (15 - 20% at that time), and sure enough they went away after the

transplant. However, one of the immunosuppressants he has to take now has

caused very mild tremors, but now it¹s only when he is holding his hands

still and consequently not nearly as frustrating as the old tremors.

And as mentioned in the other message, various meds can cause tremors as

well.

Good luck -

Betsy

> Hi guys,

>

> Starting to get concerned with the vibrations in my body, very slight but have

> started to increase throughout. My girlfriend has felt the vibrations which

> are not visible. However, I apparently have a shaky head!?! This causing her

> to panic and think it could be early stages of 'Parkinson's.

>

> Am I the only person to be suffering with this?

>

> Or is it a 'IgAN' symptom?

>

> Any advice would much appreciated.

>

> Many thanks

>

> Ian

>

>

>

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