posted
I read how others are feeling better after a couple of months abx.
I have been on them for 4 months. Had a couple of days full of energy and the rest have been crummy.
This last week, extreme fatigue, sleep a great deal during the day and at night, aches in areas where I never had aches before, ankles very swollen compared to normal a month ago. And times when my kidneys are really sore.
Have had lyme and coinfections for 15 plus years.
Is there any hope at the end of this tunnel? I think I was feeling better before I started taking abx.
On 1500 flagyl and 1500 biaxin a day.
Posts: 66 | From BC Canada | Registered: Jan 2005
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posted
I feel much as you do. I've been on Abx for 6 months now. I had a great week about 10 days ago and thought I was cured. It all came back this week with a vengence. However, the good week was my first in a couple years and makes me believe that there is light at the end of this tunnel.
On a side note, I also often feel that I was better off before I started this treatment. I had headaches, aches & pains, and brain fog, but at least I could function. My LLMD keeps telling me that this path eventually leads to getting well and the other path just leads to getting worse.
Posts: 133 | From Rocheser, MN, USA | Registered: Dec 2004
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treepatrol
Honored Contributor (10K+ posts)
Member # 4117
posted
I started feeling better in 7or 8 months but the joint pain lingered on for a while. Hang in there this takes time.
Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003
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Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
Well.. looks like it's Cave to the rescue... again!
Steve and tree also have good info to share. Steve.. hang in there. Glad you finally do "see the light". More will come your way.
Brighty.. when you see that first good day... and it will come.... REMEMBER that day and think of it often. That ONE day of relief kept me going. Soon it will be 2 days.. then 4 days.. then a week.
It will be a roller coaster ride.. so DON'T be discouraged when you lose the good days for more bad. The good ones will be back.
The only other thing to add.. from me.. would be to keep in touch with the doctor if it doesn't get better or it is "too much".
Good luck!
------------------ If you get the choice to sit it out or dance...
posted
I'm just going to tell you the truth, and that is that this can take years. I have been on abx for 4 years now, and though I do have some improvements, I relapse immediately if I skip two doses.
This situation is not true for everyone, but for a fair number of Lyme sufferers, it is. If you have autoimmune activity with your Lyme, it can be very chronic, for instance. There seem to be a number of factors that affect whether or not the meds work well.
After only 4 months, you are not in this "intractable Lyme" group at all yet. Our LLMD said 18 months minimum, at the very start.
It is true that a lot of us feel worse during treatment, because the bugs are either "stirred up" or "dying off." Sometimes I wish I had just let them lie low, although obviously, for you and all of us, the bacteria were causing enough problems for us to seek treatment.
For people like me (and maybe you, you'll know this after a couple of years) our LLMD says treatment is like Pandora's Box. It lets out a lot of bad stuff that was hiding. And you can't go back, once you've started you have to keep going (he says).
Sorry to be so blunt. I never had the expectation of getting better in 4 months, and I always wonder why some patients hear otherwise. I wish you luck and good health after a few more months of treatment...
Aniek
Frequent Contributor (1K+ posts)
Member # 5374
posted
I've had Lyme for 18 years. It was 17 years when I started treatment.
I promised myself I'd give it a year and see what happened. Even with the promise, I wanted to give up about month 6. I had increased pain in my legs, hips and feet and was tired of being on all the meds. But I told myself I needed to stick it out for 12 months minimum.
Well, at about month 7, something miraculous happened. People started telling me I looked healthier. It was amazing, especially because the pain and weakness was really bad. But then, the pain and weakness started to get reduced as well.
I'm now on month 15. I'm not cured, but I am so much better than I was. People keep telling me they see a difference, particularly in my face. So give it time, and if you need to, get treatment for the pain and swelling.
Posts: 4711 | From Washington, DC | Registered: Mar 2004
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quote:Originally posted by SteveInMinnesota: My LLMD keeps telling me that this path eventually leads to getting well and the other path just leads to getting worse.
Good statement! It took a full year before I could tell ANY difference. Hang in there!
posted
I can't stress enough the same thing. I'm on IV rocephin 6 mos now with levaquin. There are days it's unbearable thinking, but last night there was a 2 or 3 hour reprieve. Maybe there is a light at the end of the tunnel - it's just so hard to see it when you don't think and feel like you usually do.
good luck and try to have patience. I say that today - tomorrow I feel like I don't know who I am. It rots, but there are a few breakthrough moments. I just keep going, take what I have to take and maybe one day wake up and feel like I'm back in my skin where I belong. I've had physical pains that I never had before treatment, bearable but never had, mental stuff, anxiety,...It's unthinkable unless you're going throug it like most of you are. I know treatment does this, but you wonder what's the disease, treatment or maybe just me after so long of having this.
Good health and hope you have some improvement soon.
Cigi
Posts: 320 | From Upstate, NY USA | Registered: Dec 2004
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I've been on abx, cyst busters and/or other meds and treatments for 12 months now.
I would say last year, when LD came crashing down on me, I was only a 25% capable person. It was so bad that I was not able to do my professional job, and in fact, I just recently lost my job because of LD.
The first 5 months offered zero improvement in my condition. Tried different abx and cyst busters. Did nothing for me.
At about 8-9 months things had started to turn around, slowly. I would say that I was back at 50% capacity after the 9th month. And today, I'm perhaps 75%.
I think a lot of the "feeling better" is also a matter of coming to terms with the disease...you know, becoming "comfortable" and knowledgable and understand how to "handle" Lyme disease and its complications...and realizing that it's NOT just a matter of taking abx.
I attribute the turning point for my improvement to be when it finally dawned on my how complex LD really is and that it can not be treated like most other infections.
At that point I decided to address the disease from all possible sides, while still taking abx.
LD is truly a systemic, whole-body disease. Involving everything from your diet to your emiotional habits to your surrounding living quarters to the general state of your physiological health.
This disease is a real a$$hole.
I have learned, and mind you I am NOT a medical doctor, that you can not treat this disease by just taking abx.
Just taking abx may work for some people though, but my take is that for most people with chronic LD, it takes a heck of a lot more to get cured.
I'm even starting to believe that abx might even be secondary to the whole thing. Of much greater importance is it to start living healthy - diet wise and mentally, and to address other medical problems that many of us have, such as metal poisining, poor lymphatic system, hormononal imbalances, thyroid problems, yeast issues. Not to forget the usual coinfection and mycoplasma suspects.
LD is an opportunistic little sucker...and a real a$$hole at it too.
I know this may sound like stupid and vague advice, but you gotta fight back at it yourself.
minoucat
Frequent Contributor (1K+ posts)
Member # 5175
posted
brighty, I've found flagyl to be a very difficult abx to tolerate. You might want to talk to your LLMD about using tinidazole instead. It doesn't have the research behind it that flagyl does (for LD, anyway) but it is thought to be very similar in its effect, without the extreme flagyl side effects.
My experience tallies with the other responders here. I felt dreadful in the 4th month of my protocol, and started having consistently better days after the 7th month.
Since you've had some good days, I'm assuming you are not having serious reactions to meds, but that always has to be watched for.
Treating aggressively for coinfections and staying on top of yeast has been critical to my recovery. Sauna has been very helpful, and lots of different detox. I drink gallons of tea of all kinds.
posted
Actually, I probably actually felt overall a bit worse after the first few months on serious abx. However, I know I was feeling better than I had been when the herxheimer reaction was happening. The main thing, though, was that I felt hope. I had found a good doc and finally had tests that indicated that I wasn't just, uh, like, ...'imagining'... all the pain and tiredness! The hope kept me going. And I came here and had people tell me. 'Yeah Lyme sucks; but believe me, things will improve, although the speed at which they improve may be excruciatingly slow... So hang in there, and put all your effort into optimizibg your recovery! This includes diet, what kinds of limits on activities are appropriate for a chronic illness like lyme that can flare at the drop of a hat, and herbal meds that can make a huge fifference. Ask any question you can think of, always. Be sure to be a.a.a.-- Assiduous About Acidophilus. Try gingko biloba and see if that helps. Do everything you can; lyme etc. is incredibly nasty, so you need to attack on every front you can! Be wary of co-infections; other diseases that often come with lyme. Be sure to be tested and/or treated for these. I had Babesiosis and Ehrlichiosis; until I attacked those it was hit-and-miss for me. That was for years! I'm surprised you're starting out on flagyl; maybe this is something new they're trying, or maybe it has been found to be good. Flagyl (metronidazole) is usually used later in treatment to eradicate antibiotic-resistant cystic forms of lyme that develop during treatmebt with other antibiotics. Always communicate with your doc about each treatment. This can keep him or her actively thinking about your case, as well as keep you informed! DaveS
[This message has been edited by HaplyCarlessdave (edited 14 June 2005).]
Posts: 4567 | From ithaca, NY, usa | Registered: Nov 2000
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posted
With the pain, fatigue and finacial challenges it would be very easy to give up.
I look at a year ago when I had many symptoms but was able to get through many days without headaches and fatigue.
Now it's a struggle to find the energy long enough to get one thing at a time done.
I long for a few bright days to return. I should could use one right away.
Posts: 66 | From BC Canada | Registered: Jan 2005
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lymeinhell
Frequent Contributor (1K+ posts)
Member # 4622
posted
Hi there! Haven't been arund much lately because I've been feeling so much better. Abx free since November.
4 months of abx - you've seen a few good days - good for you!! That means you're going in the right direction.
However, have you done any type of detoxing to give your body a break from the dieoff?
When I read your symptoms from last week, I thought to myself - sounds herxy to me. An achey liver - yikes - that pretty much says it all. You've become one big toxic waste dump.
Do you use Milk Thistle daily? Have you tried using the foot detox patches? They really do make a difference, and you need to get rid of the garbage in your system to feel better.
I used the patches daily for a year. When I check my symptom log, and I can clearly see my big turnaround was when I started using them.
Hang tough and remember to smile..
------------------ Julie G. ___________ lymeinhell
Posts: 2258 | From a better place than I was 11 yrs ago | Registered: Sep 2003
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posted
Brighty, I've been on abx 10 months...no improvements either. Pain has been excruciating especially in my left sciatic/thigh leg area making it impossible to roll over when trying to sleep which isn't easy with my sleep apnea.
Looking for better days ahead.
bettyg
Posts: 1 | From US | Registered: Aug 2015
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