This is topic Does anyone else experience substantial air hunger while showering?? in forum Medical Questions at LymeNet Flash.


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Posted by jam338 (Member # 14002) on :
 
Does anyone else have this problem? I am wondering what it specifically relates to.

I noticed it first starting over a decade ago, long before I was diagnosed or disabled. Friends had a hot tub, but whenever I got in it I would become overwhelmed with air hunger where I had get out or sit on the edge facing the breeze after less than 5 minutes.

Now, just getting in my own shower does the same thing to me. I have noticed it being worse since I started Red Root Extract. When I take a bath I can't have the water too hot or I can't breathe. It feels like I am suffocating or trying to breathe through a hot wet washcloth. Very wierd. Any ideas about causes of this?? Thanks for any help:)

I can only imagine that those in hot humid climates must really suffer.

I was diagnosed with Lyme and Babesia Duncani within the last month, but have had symptoms for years (diagnosed FM/CFS 15 yrs).
 
Posted by Tracy9 (Member # 7521) on :
 
Interesting; I've always had this problem but never related it to Lyme. I have the exact same symptoms/feelings you describe.

I can't even stand getting a facial; the part where they blow steam in your face makes me feel like I'm suffocating.
 
Posted by adamm (Member # 11910) on :
 
Sometimes when I get really overheated--neither of the LLMD's

I've seen think I have babs, though.
 
Posted by lymeHerx001 (Member # 6215) on :
 
I have been through this with the LLMD before.

Years ago I would notice that I would get very tired and my eyes red from a shower.

Then it progressed to burning of the skin and achiness after a shower.


My LLMD said its something with the cytokines in the immune system becoming activated by the hot water.

I think it might just be the mold issue too. Showers are notorius for mold of which I get those symptoms.

Hope this helps!
 
Posted by m0joey (Member # 13494) on :
 
hi jam,

the hot water dilates our blood vessels, which rapidly leads to the orthostatic intolerance you're experiencing. It's like standing up with blood rushing downward even faster than it usually does.

-joey
 
Posted by jam338 (Member # 14002) on :
 
hi Joey, nice to hear from you again! Thanks for explaining this strange phenomenom. I plan to bring it up to our LLMD at my next visit. I'll email you on what he says:)

Joey are you still taking the Biotech Cell Guard supplements with the elements mentioned by Dr. Cheney as being important precursor elements? I completely forgot about following through on that until today. My brain went into overload after first learning I have Lyme and Babesia Duncani so I lost perspective on those discussions we were having on the other board.
 
Posted by scared08 (Member # 14695) on :
 
Hi Jam,

I've been meening to reply to this for a while; sorry for the delay! I don't know if I can be of any help, but I'll share my experience with you in hopes that it will help.

Just like you, which is kind of ironic, I too have lyme and Babesia WA 1 which I'm pretty sure is Duncai.

I was infected 18 yrs. ago; the original typical sx of flu, joint pain, fever, rash etc...lasted about 2 months. They dx me with Lupus. However after feeling somewhat better with small sx here and there.

I started to notice the same thing!! I remember going into a suana and I couldn't breath and was so weak, I could barley walk. Then I went in a hot tub, same reaction!!! Friends had to help me out as I didn't have the strength to get out. Then the hot/warm baths---same thing.

So silly now that this went on for years and I never thought anything of it; over a decade like you. I finally mentioned it to my Dr. and then the dx of M.S. was made.

After finally being dx 2 and 1/2 years ago, they did a 24hr urine hormone and endocrine test. As it turned out, this was the cause!!!

As far as me, my Adrenal gland, pitutary, hypo-thalumas, everything was not working. All of these gland produce hormones to regulate your heart rate, B.P.; well just about everything! So as a result, your body is unable to adjust to the tempature change.

I have to take warm showers with a box fan in the bathroom. NO HOT TUBS, BATHS, OR SAUNAS! And your right, living in a humid very hot enviroment is difficult. On a good day if I can make it to the river, I have to keep my legs in the water or I'm done!

Please talk to LLMD and have a 24hr urine like what I had. It can't hurt and it may help you a great deal.

Sorry this is so long! It was interesting to see someone with the exact same sx's! I wanted you to know that you're not alone and you need to discuss it with your Dr.

Take care!
 
Posted by treepatrol (Member # 4117) on :
 
I use too I noticed if I turned the hot water down so the water was just warm I did better.
 
Posted by lymeHerx001 (Member # 6215) on :
 
Hot water feels beter at first, but then I get sicker afterwards.

I was also thinking of the toxins in the water being absorbed in larger quantities by the skin because of the heat.
 
Posted by johnnyb (Member # 7645) on :
 
Jam,

Just like you and scared, I also have Lyme and Babesia Duncani.

Especially before Babesia treatment, I got the "can't breathe well" feeling while taking a warm shower, like I was suffocating.

It should improve with treatment. Hope this helps.

In the meantime, lecithin may help the air hunger symptoms. You can get it in any health food store.

- J
 
Posted by jam338 (Member # 14002) on :
 
Scared and Johnny, interesting that we share such similar and odd symptoms....but, maybe it is not as odd as we have thought since at least 3 of us seem to share very similar symptoms with it! I'll try adding some lecithin in and see if that helps, thanks Johnny for that suggestion!
 
Posted by Geneal (Member # 10375) on :
 
I have POTs and NMH and a hot shower or bath can lead to increased air hunger

Or shortness of breath along with flushing of my neck and top of my chest.

I guess I should add more cold water to the mix,

But I am usually so cold (hands and feet) when I get there,

I just can't wait to get warmed up. [shake]

I am treating for babesia/Lyme and bartonella.

I may have to live with this though chronically,

Even when I get to remission with Lyme and Co.

Good news while debilitating, it is not fatal. [Smile]


Hugs,

Geneal
 
Posted by Lymetoo (Member # 743) on :
 
Could also be MOLD or the fragrances in your soaps or shampoos!!!!

I think it was fragrances that caused mine, because I switched to unscented stuff and no longer have the problem.
 


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