This is topic Feel worse after shower in forum Medical Questions at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/1/138437

Posted by skimpbiz (Member # 4433) on :
 
I notice every time I get out of a hot shower, I'm exhausted. My neurological symptoms are worse as well, such as a hand intention tremor and buzzing in my feet.

Is this a giveaway that I have Multiple Sclerosis? I haven't been diagnosed with MS.

I've had Neuro Lyme, but for some years now, my doctor seems to believe the Lyme isn't as much a problem anymore.

All I know is showers are somewhat incapacitating and I'd love to know if that means I have MS, or if others with just lyme experience the same.

Thanks so much.

Marc
 
Posted by Rivendell (Member # 19922) on :
 
You can have neurological problems due to Lyme, some of which may not heal after treatment.

Sometimes, a person can't adjust to heat or cold quick enough.

So, if it started with Lyme, the nervous system never healed, or you still have Lyme. Sometimes MS can a manifestation of Lyme disease.

So. for you, not sure which it could be.

Just giving you my very limited knowledge on all of this.

Good Luck!
 
Posted by skimpbiz (Member # 4433) on :
 
I appreciate this thoughtful reply, Rivendell. Thank you.
 
Posted by lisaloo (Member # 12909) on :
 
I've often had this. Especially early on with lyme. Just lyme, no MS.
 
Posted by skimpbiz (Member # 4433) on :
 
I value your experience, Lisa.
 
Posted by orrn71 (Member # 50137) on :
 
So sorry you are dealing with this skimpbiz! I

totally understand this one. I feel like I avoid

showers, because it is so exhausting. I am NOT a

"dirty" person either. I used to be a shower a

day type person, but I just can't do it any more.

It just takes all my strength and energy. I have

become almost agoraphobic also, with not being

able to shower one of the main causes. My

doctor has suggested being tested for MS, but I

know I have been treating for Lyme and co-

infections pretty aggressively for several

months, but it is not getting better, but worse.

I didn't think there was a specific "test" for

MS.
 
Posted by Lymetoo (Member # 743) on :
 
Go for tepid water and see if that helps.

Keep us posted on what you find out.

I know many who have MCAS or MCAD have troubles with showers.

PS..orrn is correct .. there is no test for MS .. It's a diagnosis of exclusion.
 


Powered by UBB.classic™ 6.7.3