Been a very long time since I’ve been in this sight.
I have lyme, bart and possibly babs. I have morphea and discovered connection with lyme through this group and support of Maz.
5 years of grueling pain.
Nerve damage is extensive.
Recently I started colostrum and within a two days broke out in horrific rashes throughout my body. I was in IVIG for close to 2 years, & was surpised at this intense reaction.
I persevered. But it got to be too much to handle.
Started having drenching night sweats. SEVERE headaches. Pain in every inch of my body. The rashes started getting worse…open wounds. But once my nerve pain spread to my face i had to stop.
After a month of stopping colostrum..still no improvement.
So I took this as a sign that colostrum activated babs. Ughh…i know it’s good..bit the herxing is beyond.
The headaches are so SEVERE.
Started biaxin and just added plaquinal. Want to add Artemesia, wanted advise on best brand. I know Maz(miss u by the way..and thank you for years of support)
Thanks in advance
I’ve missed chatting with you, too, and so sorry to hear about this relapse…last we spoke, you seemed so much better. I’ll send you a PM with the brand of Artemisinin that my doc recommends.
Hope 2018 brings you and everyone here renewed health and much happiness!
Severe, swift onset RA as a result of Lyme disease
Current Meds: Biaxin (500mg BID), Tetracycline (500mg BID), Tirosint (88mcg), Liothyronine (10 mcg), Compounded Liposomal Artemisinin, LDN (3mg), Topical Progesterone,
Current Supps: Curcumin, Bovine Colostrum, ALA. NAC, Milk Thistle, Super Liquid Folate/B12/B-Complex, Probiotics, Vit D3
Supportive Measures: IV Myer's Cocktails, IV Glutathione, FIR Sauna, Gluten-free diet, Gym.