Hyperbaric Treatment (God is good!)

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Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 4:23 PM (GMT -6)   
Anyone done this? And how were your symptoms afterwards?

Quick story...

When I was first diagnosed with Lyme last year, I looked into a local hyperbarics facility for treatment. They told me how much it would cost and I had to opt out. The lady called me back within 5 minutes and asked me if I was a military veteran who had served overseas. I said yes and she told me to go to their website and there was a link there to an organization called Mission 22. This organization supports military veterans who have been deployed to combat who have developed traumatic brain injuries, neurological disorders, or diseases. I kinda forgot about the whole thing til just recently. I went to the site and applied last Friday. I received a reply from Mission 22 CEO yesterday telling me they would like to support me, but needed some info regarding my DD214 (discharge papers) and wanted info regarding my Lyme treatment. So, I responded with the info she asked for (plus a little more). I received a response less than 2 hours ago. She told me that she, herself, is a recovered Lyme sufferer and approved me for a 5-8 week hyperbaric treatment that would have cost me over $6 grand! And they would like me to start the first week in April. I will be going in for 60-90 minute treatments at least 4 times per week.

I'm about in tears over this. It has been a rough time. I've been on short term disability since November. Been getting reduced pay. My insurance through work termed out at the end of February because I am not actively working. And the insurance offered to me instead is from a company called COBRA, which would is astronomically priced per month for my family. Just no way I could pay what they wanted. So, I am having to go through healthcare.gov to get covered for now. And that doesn't start until April 1st.

I found out that I have mold growing in my HVAC system. By the grace of God I have an awesome company coming out to replace the entire system plus install an air purification system for cheaper than anyone else in the area. They usually don't finance because they are such a small company. But, they are making an exception for me.

God is good!

TDHENSLEY
New Member


Date Joined Mar 2018
Total Posts : 6
   Posted 3/13/2018 4:30 PM (GMT -6)   
Can you send me site info for Mission 22

Lapis_29
Veteran Member


Date Joined Sep 2017
Total Posts : 843
   Posted 3/13/2018 4:57 PM (GMT -6)   
nice!

that sounds great, hopefully it works for you

on lymenet there is a long ongoing thread with lots of people who have recovered using Hbot. Even the soft shell home versions work great, but you have to use it consistently, multiple times a week.

let us know how it goes for you.

Lapis_29
Veteran Member


Date Joined Sep 2017
Total Posts : 843
   Posted 3/13/2018 4:59 PM (GMT -6)   
hold on, you served overseas? did you by chance take the pyridostigmine bromide (PB), anti-nerve agent pills? they were giving them out like candy during the first gulf war.

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 5:07 PM (GMT -6)   
TDHENSLEY said...
Can you send me site info for Mission 22
Absolutely!!

http://www.mission22.com/#ourcause

Welcome to the forum!

I'm not too familiar with the Mission 22 home site. I was linked to a Mission 22 application page specifically for hyperbaric treatment through the local company's website.

TDHENSLEY
New Member


Date Joined Mar 2018
Total Posts : 6
   Posted 3/13/2018 5:12 PM (GMT -6)   
Thank you I will check it out. I am a veteran diagnosed with ALS last year and recently diagnosed with Lyme. I never believed ALS because I have been ill since returning home from deployment in 2007. God is so good I am thrilled you are getting treatment.

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 5:16 PM (GMT -6)   
Lapis_29 said...
hold on, you served overseas? did you by chance take the pyridostigmine bromide (PB), anti-nerve agent pills? they were giving them out like candy during the first gulf war.


I don't remember taking anything like that. I was in Iraq 2003-2004. We were given some type of anti malaria pills to take. But, like a dummy, I never took anything.

When we got into Baghdad, my Battalion made use of a horse track and set up operations in the stables. As you could imagine, it was filthy. We cleaned it uo. But, came in contact with a lot of bugs in the process.

Last week I spoke to a gyy that I deployed with. Last year, he was diagnosed with optic neuritis and he is now experiencing major light sensitivity and some tremors. He plans on testing for lyme and cos.

He sent me a link showing a growing number of soldiers coming back from Afghanistan and Iraq being infected with lyme and cos by sandflies. Mostly Bartonella.

Crazy stuff!

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 5:20 PM (GMT -6)   
TDHENSLEY said...
Thank you I will check it out. I am a veteran diagnosed with ALS last year and recently diagnosed with Lyme. I never believed ALS because I have been ill since returning home from deployment in 2007. God is so good I am thrilled you are getting treatment.
Crap! First off, thank you for your service. I am so sorry about your dignosis.

Are you treating lyme through an LLMD?

Check out this article, brother.

jennaslymeblog.com/sandflies-in-iraq-infect-americans-who-bring-home-lyme-disease-and-multiple-co-infections/

TDHENSLEY
New Member


Date Joined Mar 2018
Total Posts : 6
   Posted 3/13/2018 5:51 PM (GMT -6)   
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol

Lapis_29
Veteran Member


Date Joined Sep 2017
Total Posts : 843
   Posted 3/13/2018 5:52 PM (GMT -6)   
Hoagie said...
Lapis_29 said...
hold on, you served overseas? did you by chance take the pyridostigmine bromide (PB), anti-nerve agent pills? they were giving them out like candy during the first gulf war.


I don't remember taking anything like that. I was in Iraq 2003-2004. We were given some type of anti malaria pills to take. But, like a dummy, I never took anything.

When we got into Baghdad, my Battalion made use of a horse track and set up operations in the stables. As you could imagine, it was filthy. We cleaned it uo. But, came in contact with a lot of bugs in the process.

Last week I spoke to a gyy that I deployed with. Last year, he was diagnosed with optic neuritis and he is now experiencing major light sensitivity and some tremors. He plans on testing for lyme and cos.

He sent me a link showing a growing number of soldiers coming back from Afghanistan and Iraq being infected with lyme and cos by sandflies. Mostly Bartonella.

Crazy stuff!


brucellosis is what I would look at then, since it can go from horses to humans. have you looked much into that?

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 6:07 PM (GMT -6)   
TDHENSLEY said...
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol


My apologies for the assumption. My wife is ex military as well.

Where did you deploy to?

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/13/2018 6:10 PM (GMT -6)   
Lapis_29 said...
Hoagie said...
Lapis_29 said...
hold on, you served overseas? did you by chance take the pyridostigmine bromide (PB), anti-nerve agent pills? they were giving them out like candy during the first gulf war.


I don't remember taking anything like that. I was in Iraq 2003-2004. We were given some type of anti malaria pills to take. But, like a dummy, I never took anything.

When we got into Baghdad, my Battalion made use of a horse track and set up operations in the stables. As you could imagine, it was filthy. We cleaned it uo. But, came in contact with a lot of bugs in the process.

Last week I spoke to a gyy that I deployed with. Last year, he was diagnosed with optic neuritis and he is now experiencing major light sensitivity and some tremors. He plans on testing for lyme and cos.

He sent me a link showing a growing number of soldiers coming back from Afghanistan and Iraq being infected with lyme and cos by sandflies. Mostly Bartonella.

Crazy stuff!


brucellosis is what I would look at then, since it can go from horses to humans. have you looked much into that?


Interesting. Checking into that now. Thank you.

Girlie
Forum Moderator


Date Joined May 2014
Total Posts : 32588
   Posted 3/14/2018 12:32 AM (GMT -6)   
Hoagie - I am so happy for you. Please do keep us updated on your experience with the hyperbaric treatment.
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi

Girlie
Forum Moderator


Date Joined May 2014
Total Posts : 32588
   Posted 3/14/2018 12:33 AM (GMT -6)   
TDHENSLEY said...
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol


Welcome to our community, TDHENSLEY. Do you have a LLMD to treat you?
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi

TDHENSLEY
New Member


Date Joined Mar 2018
Total Posts : 6
   Posted 3/15/2018 7:51 PM (GMT -6)   
Girlie said...
TDHENSLEY said...
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol


Welcome to our community, TDHENSLEY. Do you have a LLMD to treat you?


I do have a LLMD Doctor. We have been working together for four months. I am so happy to have found this site.

Girlie
Forum Moderator


Date Joined May 2014
Total Posts : 32588
   Posted 3/16/2018 12:01 AM (GMT -6)   
TDHENSLEY said...
Girlie said...
TDHENSLEY said...
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol


Welcome to our community, TDHENSLEY. Do you have a LLMD to treat you?


I do have a LLMD Doctor. We have been working together for four months. I am so happy to have found this site.


That’s great you have a LLMD. Good luck with your treatment.

... and keep reading posts, ask any questions you have. Lots of knowledgeable people here.
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi

Dahlias
Regular Member


Date Joined Jun 2017
Total Posts : 456
   Posted 3/16/2018 7:24 AM (GMT -6)   
Hoagie, I am so happy to read this! A local friend has found that treatment very helpful. I hope it does the same for you!
"This too shall pass. It might pass like a kidney stone, but it will pass."

TDHENSLEY
New Member


Date Joined Mar 2018
Total Posts : 6
   Posted 3/17/2018 5:57 PM (GMT -6)   
Hoagie said...
TDHENSLEY said...
It was my pleasure to serve. I am not concerned with the ALS diagnosis. I intend to heal smile btw I am a woman....lol


My apologies for the assumption. My wife is ex military as well.

Where did you deploy to?


Qatar2006

1000Daisies
Veteran Member


Date Joined Apr 2016
Total Posts : 2437
   Posted 3/19/2018 3:55 PM (GMT -6)   
Oh, Hoagie. I am so happy to hear that you are able to do HBOT. (I had recommended this in a prior thread with you.) And wow - you are very fortunate to have their support. I'm truly sorry you are in need, but since you are, that is really truly wonderful that you they are able to help you. As you know, HBOT is not inexpensive. It is an amazing treatment, but it's generally unattainable due to location, availability, and cost for vast majority of people (which is extremely unfortunate).

There is a book called Oxygen Revolution that talks in great length about HBOT. Unfortunately, there is very little information about HBOT and lyme though in the book. However, the SPECT before and after (HBOT) pictures of the brains is truly inspirational!

We do have a fair amount of experience with this, and we are probably one of very few people who have experience with it with 4 members in the same family!! All four of us (me and the kids) have done HBOT - hard chamber and soft chamber. We have all had varying responses to it. However, for Kid#1, it was one of the most significant things we have done for him. It was a huge game changer for him, and because it was so expensive (and unknown), it was one of the last things we tried. But it made signficiant improvements for him. We did 40 sessions of hard chamber, and he really didn't react much during those weeks (except for few increases moods/irritability). However, after we were done, it transformed him (as his body was healing/improving from the treatments). My HBOT clinician said that some people see the effects a month after completing the series, and that was very true for his situation. (He also did repeat hard HBOT series later and then soft chamber at home too.)

Anyways, I'm happy to answer questions or share more specifics with you. I truly am excited for you and wishing you the best in HBOT journey. Please do share with us how it goes for you. Keeping fingers crossed for you!!
Kid#1: Extremely sick for several years, very difficult to treat, but doing great now!
Kid#2: Still sick now despite being treated for years but doing better (not well yet).
Kid#3: Generally good but relapsing off/on.
Me: Adv Labs positive 2016 (suspected I passed to my kids)-not as sick as others, mostly battling fatigue and yeast issues (heart/kidney issues resolved)
Treating with herbals now.

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/19/2018 5:33 PM (GMT -6)   
1000Daisies said...
Oh, Hoagie. I am so happy to hear that you are able to do HBOT. (I had recommended this in a prior thread with you.) And wow - you are very fortunate to have their support. I'm truly sorry you are in need, but since you are, that is really truly wonderful that you they are able to help you. As you know, HBOT is not inexpensive. It is an amazing treatment, but it's generally unattainable due to location, availability, and cost for vast majority of people (which is extremely unfortunate).

There is a book called Oxygen Revolution that talks in great length about HBOT. Unfortunately, there is very little information about HBOT and lyme though in the book. However, the SPECT before and after (HBOT) pictures of the brains is truly inspirational!

We do have a fair amount of experience with this, and we are probably one of very few people who have experience with it with 4 members in the same family!! All four of us (me and the kids) have done HBOT - hard chamber and soft chamber. We have all had varying responses to it. However, for Kid#1, it was one of the most significant things we have done for him. It was a huge game changer for him, and because it was so expensive (and unknown), it was one of the last things we tried. But it made signficiant improvements for him. We did 40 sessions of hard chamber, and he really didn't react much during those weeks (except for few increases moods/irritability). However, after we were done, it transformed him (as his body was healing/improving from the treatments). My HBOT clinician said that some people see the effects a month after completing the series, and that was very true for his situation. (He also did repeat hard HBOT series later and then soft chamber at home too.)

Anyways, I'm happy to answer questions or share more specifics with you. I truly am excited for you and wishing you the best in HBOT journey. Please do share with us how it goes for you. Keeping fingers crossed for you!!


Thank you so much Daisies.

I'll have to check out that book. I will be doing 40 dives as well.

I'm hoping everything goes smooth. Since Lyme and tx, I have developed some heavy anxiety. I used to be able to do MRIs. But, me last one went horribly. I tried twice and they ended up having to put ativan in my IV and put a mirror on the face cage thingy that they slide over your head so I could see out the bottom. Seems I have developed some claustrophobia. So, I am wondering if this is going to be an issue in the chamber. I have seen the ones they use, and they are pretty big and clear. But, still. I called the facility this morning and expressed my concern. She says that since she has been working there (since last July) no one that she has seen has had an issue with it. Since there's enough room for me to move around inside, and it's clear, I'm thinking I'll be ok. But, this whole ordeal has really thrown me for a loop. So, who knows.

Girlie
Forum Moderator


Date Joined May 2014
Total Posts : 32588
   Posted 3/19/2018 6:05 PM (GMT -6)   
Hoagie said...
1000Daisies said...
Oh, Hoagie. I am so happy to hear that you are able to do HBOT. (I had recommended this in a prior thread with you.) And wow - you are very fortunate to have their support. I'm truly sorry you are in need, but since you are, that is really truly wonderful that you they are able to help you. As you know, HBOT is not inexpensive. It is an amazing treatment, but it's generally unattainable due to location, availability, and cost for vast majority of people (which is extremely unfortunate).

There is a book called Oxygen Revolution that talks in great length about HBOT. Unfortunately, there is very little information about HBOT and lyme though in the book. However, the SPECT before and after (HBOT) pictures of the brains is truly inspirational!

We do have a fair amount of experience with this, and we are probably one of very few people who have experience with it with 4 members in the same family!! All four of us (me and the kids) have done HBOT - hard chamber and soft chamber. We have all had varying responses to it. However, for Kid#1, it was one of the most significant things we have done for him. It was a huge game changer for him, and because it was so expensive (and unknown), it was one of the last things we tried. But it made signficiant improvements for him. We did 40 sessions of hard chamber, and he really didn't react much during those weeks (except for few increases moods/irritability). However, after we were done, it transformed him (as his body was healing/improving from the treatments). My HBOT clinician said that some people see the effects a month after completing the series, and that was very true for his situation. (He also did repeat hard HBOT series later and then soft chamber at home too.)

Anyways, I'm happy to answer questions or share more specifics with you. I truly am excited for you and wishing you the best in HBOT journey. Please do share with us how it goes for you. Keeping fingers crossed for you!!


Thank you so much Daisies.

I'll have to check out that book. I will be doing 40 dives as well.

I'm hoping everything goes smooth. Since Lyme and tx, I have developed some heavy anxiety. I used to be able to do MRIs. But, me last one went horribly. I tried twice and they ended up having to put ativan in my IV and put a mirror on the face cage thingy that they slide over your head so I could see out the bottom. Seems I have developed some claustrophobia. So, I am wondering if this is going to be an issue in the chamber. I have seen the ones they use, and they are pretty big and clear. But, still. I called the facility this morning and expressed my concern. She says that since she has been working there (since last July) no one that she has seen has had an issue with it. Since there's enough room for me to move around inside, and it's clear, I'm thinking I'll be ok. But, this whole ordeal has really thrown me for a loop. So, who knows.


What face cage thingy? I never had one in any of the mri’s I had.
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi

WalkingbyFaith
Veteran Member


Date Joined Aug 2017
Total Posts : 1676
   Posted 3/19/2018 6:57 PM (GMT -6)   
Hoagie,

Yes, God is good!! I'm thrilled you're going to get this treatment. That's a huge blessing. Please keep us posted on how it goes for you and what it's like. I've never even seen or HBOT or thought about getting it. I seriously doubt if there's one anywhere near me anyway. There are precious few alternative medical providers around here.

I did not know so many of you were veterans. I was Army civilian employee until forced to apply for disability retirement when my symptoms got so bad and mold and chemical sensitivities drove me out of the office building. Haven't worked in a year now. My retirement package just got to OPM the end of January, so now I wait.

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/19/2018 8:07 PM (GMT -6)   
Girlie said...
Hoagie said...
1000Daisies said...
Oh, Hoagie. I am so happy to hear that you are able to do HBOT. (I had recommended this in a prior thread with you.) And wow - you are very fortunate to have their support. I'm truly sorry you are in need, but since you are, that is really truly wonderful that you they are able to help you. As you know, HBOT is not inexpensive. It is an amazing treatment, but it's generally unattainable due to location, availability, and cost for vast majority of people (which is extremely unfortunate).

There is a book called Oxygen Revolution that talks in great length about HBOT. Unfortunately, there is very little information about HBOT and lyme though in the book. However, the SPECT before and after (HBOT) pictures of the brains is truly inspirational!

We do have a fair amount of experience with this, and we are probably one of very few people who have experience with it with 4 members in the same family!! All four of us (me and the kids) have done HBOT - hard chamber and soft chamber. We have all had varying responses to it. However, for Kid#1, it was one of the most significant things we have done for him. It was a huge game changer for him, and because it was so expensive (and unknown), it was one of the last things we tried. But it made signficiant improvements for him. We did 40 sessions of hard chamber, and he really didn't react much during those weeks (except for few increases moods/irritability). However, after we were done, it transformed him (as his body was healing/improving from the treatments). My HBOT clinician said that some people see the effects a month after completing the series, and that was very true for his situation. (He also did repeat hard HBOT series later and then soft chamber at home too.)

Anyways, I'm happy to answer questions or share more specifics with you. I truly am excited for you and wishing you the best in HBOT journey. Please do share with us how it goes for you. Keeping fingers crossed for you!!


Thank you so much Daisies.

I'll have to check out that book. I will be doing 40 dives as well.

I'm hoping everything goes smooth. Since Lyme and tx, I have developed some heavy anxiety. I used to be able to do MRIs. But, me last one went horribly. I tried twice and they ended up having to put ativan in my IV and put a mirror on the face cage thingy that they slide over your head so I could see out the bottom. Seems I have developed some claustrophobia. So, I am wondering if this is going to be an issue in the chamber. I have seen the ones they use, and they are pretty big and clear. But, still. I called the facility this morning and expressed my concern. She says that since she has been working there (since last July) no one that she has seen has had an issue with it. Since there's enough room for me to move around inside, and it's clear, I'm thinking I'll be ok. But, this whole ordeal has really thrown me for a loop. So, who knows.


What face cage thingy? I never had one in any of the mri’s I had.


It's a cage mask type thing that I thought was standard for MRIs. Did you have brain and spine or just sline?

Girlie
Forum Moderator


Date Joined May 2014
Total Posts : 32588
   Posted 3/19/2018 8:13 PM (GMT -6)   
I've had two brain mri's.

First one was just my brain with the dye (ugh) for my pituitary gland.

Second one was brain and cervical spine

third, fourth and fifth were thoracic spine. (I think the third also included lumbar spine)


So 5 mri's.

I had to wear headphones - for the noise...and listened to music. Almost fell asleep a few times.

Oh, and I think something over my eyes maybe?
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi

Hoagie
Veteran Member


Date Joined Jul 2017
Total Posts : 614
   Posted 3/19/2018 8:22 PM (GMT -6)   
WalkingbyFaith said...
Hoagie,

Yes, God is good!! I'm thrilled you're going to get this treatment. That's a huge blessing. Please keep us posted on how it goes for you and what it's like. I've never even seen or HBOT or thought about getting it. I seriously doubt if there's one anywhere near me anyway. There are precious few alternative medical providers around here.

I did not know so many of you were veterans. I was Army civilian employee until forced to apply for disability retirement when my symptoms got so bad and mold and chemical sensitivities drove me out of the office building. Haven't worked in a year now. My retirement package just got to OPM the end of January, so now I wait.


Thank ypu WBF!

There might be a facility near you. It seems there are a lot in NC. Sorry to hear about your illnesses and early retirement. I'm in the middle of dealing with remnants of a mold issue at my house as well. I'd love to just pick up and move. But it's nearly impossible right now. Had a moldy crawlspace remediated and the hvac replaced. The hvac had mold in the air handler that was blowing it all throughout our house for who knows how long. Still have to disinfect all the inside of the house with a fogger and wash all fabrics in borax and an essential oil solution. Hopefully that does the trick.
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