Lymes

[Sydnie]

Hi All Lymies

Does anyone here with Lymes have UV Light sensitivity issues(no sun)? Would love to hear as havent heard anyone discuss this here.

Please reply if you know

ThanksSx

[lynnie_sydney]

Sydnie – if you type light sensitivity into the search box above, some past discussion on this will come up. Take a look at Maz's post in this thread. Lynnie http://www.rbfbb.org/view_topic.php?id=4912&forum_id=1&highlight=light+sensitivity

Be well! Lynnie

Palindromic RA 30 yrs (Chronic Lyme?)
Mino 2003-2008 100mg MWF - can no longer tolerate any tetracyclines
rotating abx protocol now. From Sep 2018 MWF - a.m. Augmentin Duo 440mg + 150mg Biaxsig (roxithromycin). p.m. Cefaclor (375mg) + Klacid 125mg + LDN 3mg + Annual Clindy IV's
Diet: no gluten, dairy, sulphites, low salicylates
Supps: 600mg N-AC BID, 1000mg Vit C, P5P 40mg, zinc picolinate 60mg, Lithium orotate 20mg, Magnesium Oil, Bio-identical hormones (DHEA + Prog + Estrog)

[Michele]

Hi Sydnie,

I had light sensitivity. For a few years before I flared with this illness, I recall needing to get high quality sunglasses. The sunlight really bothered me. I also fatigued in intense sunlight, got shaky and dizzy.

The UV of florescent lights affects me even more adversely.

I tried the MP for a while…that protocol makes you even more light sensitive.

After 9 months of a comprehensive lyme treatment, my light sensitivity is much improved. I love being in the sun! I spent 5 days at the beach this summer for vacation. 🙂 Florescent lights still slay me. Especially big box stores.

Michele

[Conniel7777]

Well… 

I have not been officially diagnosed with Lyme or any of the co-infections YET..  but I have every last stinkin' symptom…

and YES, I am very sensitive to light. I always seem to want to wear sunglasses. this seems to get worse when everything is flaring; when i am feeling good and not really flaring, the light doesnt bother me.

 

Connie

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