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Veteran Member

Date Joined Mar 2009
Total Posts : 4717
   Posted 5/11/2010 4:17 PM (GMT -7)   
I just wanted to thank you for helping everyone like you have. I appreciate it so much. And a big thank you to everyone else that posts and helps other too!....Deejavu, Razzle, Traveler and everyone. I appreciate you guys so much! If I forgot someone, I'm so sorry. My brain is rather foggy today.
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum

Veteran Member

Date Joined Apr 2009
Total Posts : 1304
   Posted 5/11/2010 7:26 PM (GMT -7)   
CG, you forgot someone...... Your self!
Bit 1972: Acute and chronic tonsillitis, UTI, miscarraige, appendicitis, hypoglycemia,  chronic neck pain w/ crushed vertibrae, chronic severe back pain, mitral valve prolapse, depression, resolution?
Bit Mother's Day 2007: Lyme, Babesia microti, hypothyroidism, EBV, HHV6, Parvovirus B19, low adrenals &misc other hormones, depression, anxiety, more of the above.

Veteran Member

Date Joined Aug 2007
Total Posts : 4400
   Posted 5/11/2010 9:18 PM (GMT -7)   
Thanks CG...and I agree with +Lyme...

Take care,
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.

Veteran Member

Date Joined Jul 2005
Total Posts : 570
   Posted 5/12/2010 6:02 AM (GMT -7)   
That's nice of you to say CajunGrl. That could be said about many people here, you included. This is a wonderful lyme forum and I've always enjoyed being a part of it as it feels like a close knit family here. You won't find a finer group of people anywhere.

I've learned so much here and have appreciated the support and kindness people have shown me when I was going through some very difficult times. This forum helped me to keep my hope alive and I will always be indebted to the wonderful people here at Healing Well for all they've done for me.

Thanks to everyone for all you have done to make this a great forum for all who participate!


Regular Member

Date Joined May 2010
Total Posts : 74
   Posted 5/13/2010 1:20 PM (GMT -7)   

You made me cry. What nice things to say. I've only just joined and I feel so connected. I was feeling so alone I cant even tell you.
So glad I found this forum. Emotional support is so great in the healing process. We are not just bodies. Healing on all levels is

So glad to be a part of this group. I'm still learning but hope to help in any way I can.

Veteran Member

Date Joined Aug 2005
Total Posts : 4325
   Posted 5/15/2010 7:55 AM (GMT -7)   
Awww shucks CG,
How thoughtful of you..  I'm not good at saying "thanks",  I have no idea why..  I just want to see people get better.
And as everyone else said, I agree that you are a blessing on this forum in every which way..
How is the moving going?   Come on, do tell..  I hope you doing okay!
It's all about the Immune System mixed with a large dose of Positive Thinking and Detoxing Daily!
This song is about my years with chronic lyme since 1995 and being in remission for over 4 years:

Forum Moderator

Date Joined May 2007
Total Posts : 36062
   Posted 5/15/2010 2:21 PM (GMT -7)   
Awww, gee!!!
CG, you've embarrassed me again with your kind words!!! I mainly do a lot of lurking, as I don't know very much about anything - but I DO like being happy!!!!! Giggle!!!
I guess this means I have to admit to reading posts that are directed at someone else now too, huh???? (blush blush!!)

Although I do agree with the others - you are a tremendous blessing to HW, as I know I wouldn't survive the first day as a Mod!!!! Tee hee!!!
It's been said:LD patients can be as ill as people w/ congest. heart failure & in as much pain as post-op patients.

New Member

Date Joined Oct 2011
Total Posts : 12
   Posted 10/31/2011 4:42 PM (GMT -7)   
Hi all,

I have been following threads on here for a while, but reading this one is what made me decide to join. I love the support you guys give each other. Anyhow, I have had health issues for about 8 years. I am guessing it's probably Lyme (I had an equivocal test, then did Igenix and had + bands).

I think I partly waited to join as somehow joining was like admitting to having it, and that has been a scary reality to face.

Anyhow, I long story short I have done the Mepron and Zithromycin for Babesia,right up until my liver couldn't take anymore. Then I found out I also have Brucellosis. Took meds for that, until liver couldn't take it anymore. Now I have to address the lyme, but don't want Rx. A friend told me about Envita in September, so came back here to research and found BWB's thread about Hansa. I have been reading all the Hansa stories I can get my hands on ever since.

I summarized the info in an effort to make sure I'd read them all, but that post got a cold reception. So anyhow, I am going to Hansa in November. I wanted to thank folks on the forum for their stories, especially you BWB, I am a detail fiend (used to do chemical engineering) so appreciate your information. I also recall there were folks who wanted to go, but money was tight. I cant recall all of those names, if anyone know someone that might benefit from sharing my room, please have them contact me.

Thanks again all, you have been a support network for me indirectly up until now. I will be sharing my Hansa story too :)

All the best,

New Member

Date Joined Oct 2011
Total Posts : 12
   Posted 10/31/2011 6:28 PM (GMT -7)   
Hi! Good luck to you at Envita, I actually had heard of that first. Maybe I could catch you offline to hear your two cents on Envita at some point? One can never research too much on this stuff, right? I watched your video, nice job! :)

All the best,
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