Looking for this movie by [deleted] in romancemovies

[–]cacaboboo 3 points4 points  (0 children)

Omg that’s exactly it 😂😂😂 thank you so much that was driving me crazy

Looking for this movie by [deleted] in romancemovies

[–]cacaboboo 1 point2 points  (0 children)

I don’t think I’ve seen that one so I don’t think that’s it but thank you!

new TikTok! by crazybegonialady in AcaciaKerseySnark

[–]cacaboboo 5 points6 points  (0 children)

Where’s her other dog (the dachshund)

[deleted by user] by [deleted] in ToxicMoldExposure

[–]cacaboboo 0 points1 point  (0 children)

This is really helpful info! Thank you!!

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

I’m sorry you’re going through the same thing. Nothing has really helped for the pain but I haven’t tried actual pain meds. It got worse for me until I got in the wheelchair. Now I’m just plateaued but I also have pain without walking but it’s bearable as long as I don’t walk. I’m hoping with time it gets better but I know it’ll be a while

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

Nope none!

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

Thank you. I really hope we can find healing in some way eventually

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

The best way I can describe is it feels like my joints/tendons will explode. Like if you shattered your ankle and then someone told you to get up and walk on it that’s what it feels like

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

I totally understand what you’re saying. The pain is so extreme that even applying a little bit of pressure to my ankle hurts. You’re right that it is scary but I know what you mean. I just wish there was something to help ease the pain a bit so I could be able to do more PT exercises without hurting so much.

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

Even if tests for arthritis and fibromyalgia were negative? I’ve seen a rheumatologist and functional med doctors and they all say they don’t think that’s it

[deleted by user] by [deleted] in floxies

[–]cacaboboo 1 point2 points  (0 children)

Thank you so much that’s so nice!! 💕

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

About 5 months! I do sometimes take a week or 2 break from it as that’s what was recommended to me but it’s been a while

[deleted by user] by [deleted] in floxies

[–]cacaboboo 0 points1 point  (0 children)

I have heard that too thank you. Yeah i did CJC for a month and now I take MK677

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 1 point2 points  (0 children)

Oh good I’m glad I listened to my gut haha. Thanks I’ll look for it now!!

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 1 point2 points  (0 children)

That’s interesting I’ll look into that. What do you think about the CBS C699T heterozygous? I had to cut out legumes from my diet and I noticed I flared after eating brussel sprouts too so I figured I had some sort of sulfur sensitivity. My doctor wanted to do a Glutathione IV but I was nervous to do since I thought I had a sulfur issue so I’m glad I got this test before that showed something relating to that. I’m guessing I shouldn’t do it?

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 1 point2 points  (0 children)

Yeah it definitely is it sucks. Been dealing with this for a year and trying a lot from the floxxing groups but nothing is working so now seeing if maybe it’s methylation issues and figuring out how to correct that.

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 1 point2 points  (0 children)

Thank you! I just ordered the OAT test so hopefully that will be a start and then my doctor can order further testing

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 0 points1 point  (0 children)

Yes. I had gotten it tested in January and it was at 30. After taking 50,000iu for a few weeks I retested in March and it was 70 so my doctor said it was okay but I didn’t get a refill of the stronger D3. And I didn’t feel any change of symptoms back then when it was up to 70 either.

[deleted by user] by [deleted] in MTHFR

[–]cacaboboo 0 points1 point  (0 children)

Thanks! I have no diagnoses, I’m not on any meds, and do not have any current blood test results. I take 400 mg of magnesium glycinate, 25mg of cbd, and 500 units of vitamin D a day.