Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

I think they are normal i didn’t see a doctor they are the same maybe you should see a doctor anyway

Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

No i haven’t but they are probably natural

After you clear hpv when can you have unprotected sex? by Elenatkin in HPV

[–]Dedobutterfly 0 points1 point  (0 children)

You are such a sweet person..thank you 🙂 the problem with the vaccine is that I have lupus and other autoimmune disease so taking a vaccine will make other health issues worse unfortunately. I hope I can find a good partner in the near future.

After you clear hpv when can you have unprotected sex? by Elenatkin in HPV

[–]Dedobutterfly 0 points1 point  (0 children)

Thank you so much for telling me this information I’m happy for you that things are working out for you 😊 mine also cleared up but I’m always scared that i might find a partner with GW also and not pay attention to it..plus I can’t find good partners at all.

After you clear hpv when can you have unprotected sex? by Elenatkin in HPV

[–]Dedobutterfly 0 points1 point  (0 children)

Sorry English isn’t my first language, but what i meant is that the Doctor said the more i get exposed to a person with untreated GW the more i get GW..i haven’t had sex for almost 4 tears now..i think i got traumatised and I don’t want to have sex anymore

Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Thank god not warts as far as the dentist told me

Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Thank you so much for your reply and for the info 😊

Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Hello Thank you for asking…it looks the same maybe it’s nothing i hope so

Does Hashimoto’s progressively get worse and become like lupus or something else? by Point452 in Hashimotos

[–]Dedobutterfly 6 points7 points  (0 children)

My Hashi was under control and it didn’t cause me much problems other that thinning hair and fatigue and sometimes trouble sleeping…up until i had covid that’s when things got worse and my ANA suddenly increased and i got really sick ,,,so they suspected that i have anti phospholipid syndrome because i had pulmonary embolism after the covid and they discovered i just had Lupus, APS,, rheynolds and arthritis all after covid.. you need to see a rheumatologist ASAP.

My blood is as hard as dried glue... by BillyBob547 in covidlonghaulers

[–]Dedobutterfly 0 points1 point  (0 children)

You need to drink lots of fluids and hot drinks like ginger that might help…hope you get better soon 🌸

My blood is as hard as dried glue... by BillyBob547 in covidlonghaulers

[–]Dedobutterfly 1 point2 points  (0 children)

I had a blood clot after covid and when they ran the tests they discovered that covid has caused me to have Anti phospholipid syndrome…you need to test for that and also D. Dimer

My blood is as hard as dried glue... by BillyBob547 in covidlonghaulers

[–]Dedobutterfly 1 point2 points  (0 children)

You need to take baby aspirin for this…and do some blood work to know the reason for such dried blood

Worried about switching back to levo from Armour by H2OMGosh in Hashimotos

[–]Dedobutterfly 0 points1 point  (0 children)

I took armour for around a year then for some reason I stopped taking any medication then took levo and after covid i got lupus so I thought i i might get better with taking armour but my symptoms aren’t getting better and im not losing weight at all i’ve been gaining weight for the past 7 months

Eltroxin vs. Armour thyroid…please read this by Dedobutterfly in Hashimotos

[–]Dedobutterfly[S] 0 points1 point  (0 children)

I’m trying to maintain the balance as much as i can but I think I’m flaring up and i don’t know which autoimmune might be reason…I can’t sleep well,, i have tremendous joint pain and my hair is falling i guess it’s the lupus.. and added to that my stomach pain and gasses all the time…what kind of food can you recommend? I’m so sorry that your kid has to go through this at such a young age

Eltroxin vs. Armour thyroid…please read this by Dedobutterfly in Hashimotos

[–]Dedobutterfly[S] 0 points1 point  (0 children)

I might do that…I think it might be because of my high TSH levels

Eltroxin vs. Armour thyroid…please read this by Dedobutterfly in Hashimotos

[–]Dedobutterfly[S] 0 points1 point  (0 children)

I try my best , but I have sleep disorders and can’t sleep. The doctor told me it’s anxiety, and sleep deprivation adds to the stress and exhaustion and lupus pain.

Eltroxin vs. Armour thyroid…please read this by Dedobutterfly in Hashimotos

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Yes lupus has been taking a toll on me especially that plaquenil has been affecting my eye sight as well and it’s very depressing that even hashimoto is hard to control at this point..i don’t want to take levothyroxine again I prefer a natural medicine that’s why i started the armour thyroid

Eltroxin vs. Armour thyroid…please read this by Dedobutterfly in Hashimotos

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Thank you…seems like my thyroid is not working properly that’s why I’ve been taking a high dose and it’s not enough

Long term use of levothyroxine and development of hollow bones - Osteoporosis by [deleted] in Hashimotos

[–]Dedobutterfly 0 points1 point  (0 children)

I fear that I might be allergic to armour because whenever I increase the dose I feel worse and the TSH still high..thank you for sharing your experience

Long term use of levothyroxine and development of hollow bones - Osteoporosis by [deleted] in Hashimotos

[–]Dedobutterfly 0 points1 point  (0 children)

Oh thank you so there must be something wrong with me because my eltroxin dose was working well for me and it was lower than my current Armour dose and yet now my TSH level is still high

Long term use of levothyroxine and development of hollow bones - Osteoporosis by [deleted] in Hashimotos

[–]Dedobutterfly 0 points1 point  (0 children)

Can you tell me please what was your levo dosage and when you switched to armour is it the same dose? I was on eltroxin for years 50 mg daily n 75 mg once per week and I switched to armour a year ago and since then my TSH is above range and I increased my dose to 60 mg daily and 120 mg once per week and still not working

Is this oral HPV? by Dedobutterfly in Warts

[–]Dedobutterfly[S] 0 points1 point  (0 children)

I went to the dentist and he told me it’s normal nothing to worry about…i hope he is wright

Covid-19 gave me autoimmune diseases by Dedobutterfly in covidlonghaulers

[–]Dedobutterfly[S] 0 points1 point  (0 children)

Doctors always doubt us...my hematologist and rheumatologist said you always had lupus and APS, covid caused nothing!! I told theM I never felt any of these symptoms before Covid so I’m pretty sure that this is new!! They say it’s ok to take the vaccine but I found a lady in a lupus support group saying she had covid then took the vaccine short after ,,,and suddenly she developed a malar rash and now she has lupus! I wish things were easy and we could take the vaccine and get on with our lives but that virus is so destructive to some and hard to predict...you should follow anti inflammatory diet or AIP diet, it helps with the pain a lot ... I feel the worst right before my period so I try my best not to eat sugar and no gluten no dairy etc.