This is topic Too fatigued to talk? in forum Medical Questions at LymeNet Flash.


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Posted by BartonFink (Member # 10818) on :
 
Hello

Have you had fatigue that bad? I have had that for weeks now. Have you found anything to help with it? Now I'm even too fatigued to type more... [Frown]

BF
 
Posted by mtnwoman (Member # 8385) on :
 
Yes, I've known fatigue that bad. At my worst I found that talking exhausted me.

Try keeping blood sugars even by avoiding overly refined foods like fruit juice, cereals, granola bars, etc.

Hopefully you are not vegetarian. I found protein each meal helped me.

Have you ferritin checked -- ideal between 35-75. It's your iron stores.

You might check one of those saliva adrenal tests to see what your cortisols are doing.

Check your thyroid: TSH (want <2.00) and free T3 and free T4.

I hope you are under the care of a good integrative doc who can explore what may be going on? Good luck!
 
Posted by Lymetoo (Member # 743) on :
 
Are you being treated for babesia? I would suspect that to be the culprit. Sorry you're so exhausted....been there.... and it's rough!
 
Posted by BartonFink (Member # 10818) on :
 
I think my ferritin was something like 45.

Yes actually I already ordered a saliva test (adrenals, thyroid, sex hormones) so hopefully that will tell something. My TSH was 2.6 the last time it was checked (blood test) and frees were pretty low.

I have a pretty good doc yes but even she is clueless...

Of course, this might have something to do with Biaxin that I just started yesterday.
 
Posted by BartonFink (Member # 10818) on :
 
I dont think we have babesia in this country.

My only treatment is Biaxin at the moment, just started it. Plus many supplements.

quote:
Originally posted by Lymetoo:
Are you being treated for babesia? I would suspect that to be the culprit. Sorry you're so exhausted....been there.... and it's rough!


 
Posted by painted turtle (Member # 7801) on :
 
YES!

I've been in places of not being able to reach in for the words, the response....as I lay in bed and the voice of my partner was just an echo of a fade.

Completely energy less.

I think it was the brain inflammation at its worst.

I should count my lucky stars this part of the "fatigue" has improved with antibiotic treatment.
 
Posted by EWT1638 (Member # 11315) on :
 
I understand what you are talking about. Sometimes I will get so weak (suddenly!) that I can't ever think straight. I think it must be something akin to having a stroke...you can't get your thoughts (as disorganized as they are) to your mouth!
 
Posted by bejoy (Member # 11129) on :
 
I've started addressing mitochondrial dysfunction, and it seems to be making a big difference with my energy level. This is the power center of the cells.

You might want to look at info on mitochondria, and supplements including:

CoQ10
Acetyl L-Carnitine
D Ribose
NADH
B complex vitamins

Good luck.
 
Posted by lymednva (Member # 9098) on :
 
Years before my Lyme dx I experienced this and was helped when I was treated for dysautonomia.

I recently tested positive for Babs and will be interested to see if my treatment, which I just started, helps this area of my health. It would be great news if it did because it's the most physically disabling problem I have.
 
Posted by Skyler (Member # 11549) on :
 
I have experienced this too. I am so sorry this is happening to you.

I don't know any advice for dealing with it, but hang in there!

I'll be sending good thoughts and a little energy your way!
 
Posted by BartonFink (Member # 10818) on :
 
quote:
Originally posted by bejoy:
I've started addressing mitochondrial dysfunction, and it seems to be making a big difference with my energy level. This is the power center of the cells.

You might want to look at info on mitochondria, and supplements including:

CoQ10
Acetyl L-Carnitine
D Ribose
NADH
B complex vitamins

Good luck.

Interesting. I might try those. How big doses are you using?
 
Posted by bejoy (Member # 11129) on :
 
http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=056445

Here's a recent thread with a couple of links to good articles.

There are some good research articles on CoQ10 and Parkinsons floating around out there. As I recall, they recommend up to 2400mg daily. I've been taking 1400 daily for the past five days, and I notice a big difference(but the stuff is really pricey.)

I'm not sure my amounts are going to give you a good base line or starting point, as I am still experimenting. You could ask others if you post a new thread.
 
Posted by Dave6002 (Member # 9064) on :
 
At my worst, talking, listening, typing and watching TV, all made me mentally exhausted.

It lasted for a month or so.

With abx treatment, it's gone for a while.
 
Posted by David95928 (Member # 3521) on :
 
Has this become worse since starting Biaxin? IF so, you may be herxing.
 
Posted by dmbfan (Member # 11948) on :
 
Yes, I get this when herxing. My dr came me similar herbs as Bejoy posted above. I am doing better now.
 


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