This is topic How long do we treat this disease? in forum Medical Questions at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/1/120972

Posted by sick (Member # 9143) on :
 
I have been on different antbiotics for over 6 years now. Yes I am better in a lot of ways but others not so much.

I still sweat if I do anything at all. I mean it just pours off of me. When I use to have hot flashes I never sweat like this.

I have no endurance at all. I can't fold a load of clothes without resting several times. Can't carry anything very heavy.

I still suffer from air hunger also.

How do you know how long to treat. It seems like I am just stuck and not really getting any better or worse. And to make things worse I no longer have a LLMD.

SICK
 
Posted by beths (Member # 18864) on :
 
Did you treat babesia?

6 years seems a long time for little progress-maybe try herbs?
 
Posted by triathletelymie (Member # 26456) on :
 
Have you treated all co-infections?

Perhaps if you could give a little more info, you may get more ideas...???
 
Posted by map1131 (Member # 2022) on :
 
A couple of your lines really struck a cord with me....even though I've struggled with lyme & co for years, when I noticed even less endurance and the simple things like doing wash would leave in resting??

I finally decided it was time to get a cardio doc involved, just to make sure. All the tests revealed 100% blockage in right cornary artery.

TBTG, my body had built a little vessel to by pass the blockage. All these years lyme & co had covered up sx that healthy people feel.

So please make sure some of your sx aren't your heart screaming for help.

Also there are many options if abx failed you. Six years is a long time. Have you thought of trying alternative methods to control the bacteria load, like herbs, rife, naturopath doc for detox of heavy metals and parasites?

Iowa, has support groups. Have you looked to see if any are near you?

I was 42 yr old when this nightmare began, much too young to think about heart damage.

Pam
 
Posted by sick (Member # 9143) on :
 
map1131 I have had both knees replaced and had a physical before each one. The last one I had done last April. Wouldn't the heart test they do then have showed a blockage?

I haven't tried herbs because I feel like no more then I know about them I would be wasting what little money I have on them.

I don't know of any naturpath doc and I could not afford one if one was even close to me.

I don't know what the rifles cost.


sick
 
Posted by sick (Member # 9143) on :
 
triathletelymie
I am not sure what my doctor has treated me for. When I seen him he would always just talk to me and ask questions and when he was done he would write out the prescriptions. He never really told me much and maybe I never knewn what questions to ask.

sick
 
Posted by sick (Member # 9143) on :
 
You know I started getting sick when I was in my 20's. It took over 50 some years and many doctors before I knew what was wrong with me. Finally found out I had chronic lyme when I was tested by the Igenex lab.

I am now 64 and I don't know what you should feel like at this age. Maybe this is as good as you get from treatment and the rest is just my age. I just know both of my folks were very healthy until they were in their 90's. They never slowed down until they were in their very late 80's.

sick
 
Posted by pug7 (Member # 36995) on :
 
I am also in my early 60's and love what you said about not knowing what we should feel like at this age. I take a Tai Chi class at the senior center and find that most people have some issue/s.

I was also on antibiotics for 6 years, with some progress but not that much. I also developed positive lupus tests while in treatment.

Every time I tried to get off antibiotics, I got really sick, and my LLMD would tell me that I was one of those who would need them for life. I sought help from a functional medicine doctor (covered by insurance; like you, I have issues with cost), who helped me get off after explaining there is a 2-3 week withdrawal period when getting off long term antibiotics, partly because the meds are anti-inflammatory, and also because the immune system has become dependent on them.

I have been off for a few years now, and overall feel better off than I did on. There are residual GI and,in my experience, food allergy issues after getting off long term antibiotics. I can no longer eat quite a few things. But getting off dairy and gluten and a few other things also did more for my neuro problems than antibiotics.

If I were you, I would try getting off, but expect a few weeks of illness as you do that, and don't blame it on a relapse of Lyme, blame it on withdrawal. See how you feel in a month, then a few months, then a year. There will be other things that can help, that will become apparent or that others can tell you about, but you really don't have to go crazy with supplements and other costs, in my opinion.

Accepting limitations that remain and enjoying what you can do seems key, in the long run, to me.
 
Posted by nefferdun (Member # 20157) on :
 
Sick, I am 65 and I understand how you can wonder if some of your mental and physical problems are due to age especially when it has been such a long time since you felt well.

But I am closer to well now than I have been in years and I feel really good. I am not running a marathon but I can climb two flights of stairs without collapsing - in fact, without losing my breath.

You need to pay better attention to what infections you have treated. What drugs have you been on? Profuse sweating is usually a sign of babesia microti.

Once you treat everything (don't forget protomyxzoa) you will get better.
 
Posted by sick (Member # 9143) on :
 
When I go off of the antibiotics I am fine for 2 or 3 months then I start to sweat profusely and some of my lyme disease symptoms return so then I assume I need to start back on the antibiotics again.

I have gotten over the terrible fatigue so I don't sleep all the time like I use to. I know that the doxycycline helped with that.

May I ask neuro problems was you having?

How did you know if you was over the lyme disease. Did you get tested again?

I appreciate any advice you have as I am at a point where I don't know what to do next.

Did you take any supplements that you thought helped you?

sick
 
Posted by gigimac (Member # 33353) on :
 
No way!! I'm going to have to deal with withdrawal if i get off abx? I can't even begin to deal with that.

I am gonna start a new post.
 
Posted by sick (Member # 9143) on :
 
nefferdun

I know what antibiotics I have taken but I guess I don't know what co infections each of them treat. Is there a way of telling what each drug treats?

You say once you treat everything you will be better. I'm not sure what everything would consist of. Is there some where I could read about that?

I read as much as I can about lyme disease but I have problems with my memeory so it really don't much good. As far as I am concerned that should be the doctors job. I don't feel like I have had a very good LLMD but it was the only one I could go to.

sick
 
Posted by sick (Member # 9143) on :
 
Does anyone else have any thoughts or ideas?

sick
 
Posted by dbpei (Member # 33574) on :
 
sick, here is a good link explaining the co-infections and the drugs that are often used to treat. Hope this helps.

http://www.truthaboutlymedisease.com/phpBB3/viewtopic.php?f=10&t=313
 
Posted by sick (Member # 9143) on :
 
dbpei

Thank you Thank you Thank you! Bless your heart.
What a wonderful site you sent me.
I started reading it but will have to read more later. I seen it told what drugs are used for different co infections. I needed that so much.
I am going to print some of it as my memory is terrible. That way I can look back as needed.

I know we should be able to find the answers by ourself but some us are sick enough we just can't do that.

I only hope I can help someone as much as you have helped me.

sick
 
Posted by dbpei (Member # 33574) on :
 
sick, your mailbox is full. I tried to respond to your PM.

I hope you find some relief soon. The above website is an excellent resource, but it looks like you can no longer register for that forum.

An awesome website that has also helped me tremendously is

http://www.treatlyme.net/

Best wishes! PM me any time. I am a social worker by profession and I love helping people!
 
Posted by sick (Member # 9143) on :
 
Thank you. I cleaned out my mailbox.


sick
 
Posted by glm1111 (Member # 16556) on :
 
sick,

PLEASE look into treating for parasites. I didn't start getting well until I treated this often overlooked co-infection. Parasites/worms can play a MAJOR role in Lyme disease.

Google parasite symptoms and check the symptom list at Humaworm. One mos of tx is never enough and has to be ongoing till symptom free and then maintenance. It can take saeveral yrs to get rid of parasites.

Gael
 
Posted by Lymetoo (Member # 743) on :
 
BABESIA
 
Posted by sick (Member # 9143) on :
 
glm1111 Oh boy I have avoided that one. I have already been on antibiotics for years.
What did you use to treat parasites?
Will the Rifle get rid of them?

Lymetoo I thought about Babesia but you know I only sweat on my face, hair and neck. I thought you would sweat all over with it.
Do you think the Rifle will get rid of parasites?

sick
 
Posted by glm1111 (Member # 16556) on :
 
I used antiparasitic herbs like Parastroy, Humaworm, Hanna Kroeger Wormwood Combo, cloves, digestive plant enzymes and salt/c.

The antiparasitics and salt/c also worked to get rid of my babs and bart. To my knowledge, I don't think rife alone will get rid of parasites.

Gael
 
Posted by Lymetoo (Member # 743) on :
 
You don't have to have every symptom to have babesia.

RIFE can help get rid of yeast, parasites, Lyme, babesia, bartonella, whatever you have!
 
Posted by sick (Member # 9143) on :
 
Oh my I don't even know where to start.

sick
 
Posted by Lymetoo (Member # 743) on :
 
Babesiosis


As with other co-infections, there is a lot of overlap of symptoms between Lyme disease and Babesiosis. An accumulation of the following signs and symptoms probably warrant testing and/or treatment of Babesiosis:

___Chills

___Fatigue and often excessive sleepiness

___High fever at onset of illness

___Night sweats that are often drenching and profuse

___Severe muscle pains, especially the large muscles of the legs (quads, buttocks, etc.)

___Neurological symptoms often described as "dizzy, tipsy, and spaciness," similar to a sensation of "floating" or "walking off the top of a mountain onto a cloud"

___Depression

___Episodes of breathlessness, "air hunger", and/or cough

___Decreased appetite and/or nausea

___Spleen and/or liver enlargement

___Abnormal labs (low white blood count, low platelet counts, mild elevation of liver enzymes, and elevated sed rate)

___Headaches (migraine-like, persistent, and especially involving the back of the head and upper neck areas)

___Joint pain (more common with Lyme and Bartonella)

___anxiety/panic (more common with Bartonella)

___Lymph gland swelling (more common with Bartonella and Lyme)
 
Posted by sick (Member # 9143) on :
 
Thanks Lymetoo
 
Posted by tickled1 (Member # 14257) on :
 
Have you tried LDN (low dose naltrexone)?

Have you had your thyroid checked?

Do you have MTHFR, KPU, or HLA-DR genotypes?
 
Posted by sick (Member # 9143) on :
 
tickled1

The only one of your questions I can answer is yes I have had my thyroid checked and am on thyroid medication.

The rest I will have to look up as I do not know what all it is. Never heard of most you mentioned but will check it out tomorrow.


sick
 
Posted by minimonkey (Member # 8693) on :
 
Sick -- I also think your symptoms sound like Babesia. I sometimes had full body sweats, but often just my neck and head would sweat.

Generally babesia is treated with Mepron or Malarone -- sometimes quinine drugs are used. It's hard to get rid of Babesia -- some strains of it are worse than others... but MAN I felt better after we addressed mine.

Do you get head pain?
 
Posted by tickled1 (Member # 14257) on :
 
I have subclinical hypothyroidism. All my regular docs said my thyroid was fine according to results but I went to an integrative doctor that did some additional testing and found I was hypothyroid. I am on Tirosint now. I was on Armour before that but the Tirosint is working out better.

Many docs say thyroid is fine b/c they don't do the additional testing when in fact you could be hypothyroid and treating can make all the difference in the world.

Low Dose Naltrexone can also be very beneficial. It is an immune modulator and is used for Lyme, MS, Parkinson's and other autoimmune diseases. Have to start low and slow w/this.

Have you addressed yeast at all?

All the other things I mentioned like the MTHFR, KPU and HLA-DR are detox issues. I found out I have MTHFR and am homozygous C677T for that which means I can't convert folic acid or B12 to it's active, or methylated, form so I have to supplement these in their already active/methylated form.

Being deficient in these can cause serious symptoms. I have noticed improvement since starting "B Supreme" by "Designs for Health". If you are unable to get the testing done to find out if you have this you'd have nothing to lose by supplementing and see how it goes. It wouldn't hurt. Just make sure you don't take a regular B Complex supplement. It has to be in it's active form and I can assure you the one I mentioned is.

Are there integrative, alternative, osteopathic, homeopathic or naturopathic doctors in your area that take your insurance since $ is a factor? Don't waste your time w/conventional doctors. Good luck!
 
Posted by gmb (Member # 23562) on :
 
I too never really had night sweats.. so I thought most of my symptoms were Lyme and Bart.

I started treating Babs first and symptoms flared from there. My new night sweats are as you describe, only lightly on my face, neck and hair.

I also occationally sweat in same areas durig the day when under minimal physical excersion or high stress.

Its tough to determine cause with so many things wrong with us. I just call it a big science project trying to get well.

gmb
 
Posted by Catgirl (Member # 31149) on :
 
Sick, listen to glm1111. The woman is wise. I used to ignore her posts, but she turned out to be right with me. She is so right, it's simply not worth it to ignore this issue. I've made more progress treating parasites (in just a few months) and detoxing heavy metals than I ever did on abx.

IMO, parasites are a HUGE issue with lyme. Unfortunately, most of the lyme docs don't even have a clue about them, so we are all left to handle them ourselves.

It has been my experience that many people think because we live in a first world country that parasites don't exist here. Wrong. They come with the tick, food, water, etc. Parasites are just as much a part of nature as we are. I just got higher doses of them from ticks.

Also heavy metals. We have to detox them. Gigi knows more about metal detoxing than anyone I've ever spoken to or chatted with on line. Another very wise woman. I would read every single word she posts. IMO, there is a heavy metal parasite connection that should not be ignored to get well. Gigi explains this really well.

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=118683;p=0
 
Posted by sick (Member # 9143) on :
 
Oh I will. I listen to everyone who posts and take it quite seriously.

sick
 
Posted by D Bergy (Member # 9984) on :
 
Rife type frequency treatments totally eliminated Babesia in my wife. It took me three rounds of treatments to do it, but I was pretty green at it at that time. It would be faster for me now.

I have never used it for parasites.

It has brought my wife to 95 percent normal by greatly reducing, but not eliminating Lyme. Not sure of Bart is completely gone, but if it is there, it is not causing her any symptoms.

It will not cure everything, but for a one time investment, it is probably one of the cheapest treatment methods you can use for multiple infections, for as long as needed.

I still run the frequencies once in a while if she starts getting joint pain, but it is far better than the limited alternatives available to her.

I hope you can find some effective way of killing what sounds like Babesia.

Good luck

Dan
 
Posted by cozynana (Member # 34270) on :
 
I too would say that Gael is very wise when it comes to parasites. I talked to her personally when I was looking for answers.

I have used ipil-ipil,alinia,Hannah Kroeger Wormworm combo, and something else, escapes my mind.

I am going to try salt/C protocol soon.

I have associated the terrible sores and swelling of my tongue to parasites.

I had a geographic tongue and lesions until I treated for parasites.

The size of my tongue is about 1/2 of what it used to be.

My bowel and hip pain has greatly diminished after treatment of parasites.

I don't think I have expelled all parasites yet.

I may need to try salt/C to get rid of the rest of them.

I also know I have only been on parasite protocol for about two months.

This is not long enough to completely get rid of all parasites.

I am in for the long haul.
 
Posted by sick (Member # 9143) on :
 
D Bergy
What caused her joint pain? I didn't know it would help that.
sick
 
Posted by D Bergy (Member # 9984) on :
 
Lyme mostly, but Bart also caused some pain and swelling in the ankles.

Her first and main symptom was joint pain which was worst in the knees and ankles.

Most all joint pain is caused by pathogens of one kind or another. If the pain came shortly after a tick bite, you can narrow down the list of pathogens considerably.

Dan
 


Powered by UBB.classic™ 6.7.3