APS, Menopause & getting relief - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,411 members10,622 posts

APS, Menopause & getting relief

AnnieAxVale profile image
16 Replies

I know I cant have any HRT but just wondered if anyone can recommend any remedies that have helped them through it. What am finding most difficult is the sweating. Its not just night time its day time too and not always when am flushing either. Palms of me hands are sweaty as is my feet which is so annoying. Also starting to get a bit crabby more than I have been.

I take Vit B6 but dont think I am taking enough. Holland & Barrett sell 100mg tablets and my pharmacist recommended 20mg dose as highest I can take, but I knew you could take more so thats an option.

I cant take Oil of Eve Primrose because of my thyroid (which also means alot of other herbal and vit remedies too possibly.

Anyone got any recommendations of what else I might be able to try or at least research?

Thanks :) ( I am not on warfarin but Heparin)

Written by
AnnieAxVale profile image
AnnieAxVale
To view profiles and participate in discussions please or .
Read more about...
16 Replies
HollyHeski profile image
HollyHeskiAdministrator

I was given a blood pressure medication (Clonodine), to help with the sweats. I had had a hysterectomy & was having to go 'cold turkey'! My blood pressure was always normal anyway & didnt effect it either. It helped but didnt stop them completly.

AnnieAxVale profile image
AnnieAxVale

My thyroid is fine.. was checked very recently and had a visit to the GP this morning who offered me Clonodine which I said I would think about as I dont like to start new drugs unless absolutely necessary.. going to go down the natural route for now and see how it goes.. ty all :)

AnnieAxVale profile image
AnnieAxVale

Will do... am very careful about what I take, prescribed or not :)

MaryF profile image
MaryFAdministrator in reply toAnnieAxVale

I have Thyroid problems, and don't rely on just the TSH test being the only angle tested with my Thyroid. I privately pay for more extensive tests which show everything, doctors often and usually only do the TSH which is not a true indicator of what is going on. MaryF

ZRHONDA profile image
ZRHONDA

I take 2K mgs of vitamin D and I also found out the blood pressure medication, Clonidine helps with the hot fashes and sweating so my doctor switched me to that. I'm on a higher than usual dose but I take my blood pressure 4 to6 tines a day, if it goes below a certain threshold I must refrain from taking the clonidine. For some reason Prozac has helped me greatly. I also take a large dose of 80mg. Those are the only things that have helped me. Of course you must be closely monitored by your physician. I had a full hysterectomy after being diagnosed with Lupus SLE and Factor 5 Lieden. So HRT was out of the question. I hope you are able to get some relief. I know how awful it is to break out in a full body sweat while in a meeting or in public. I carry bandanas in my purse always to blot my face as well as baby wipes and deodorant. I feel for you and again I hope you find something that works for you. GOD BLESS.

glovebox profile image
glovebox

I've been using serenity cream for the last 2 years and have been amazed by the results. My consultant recommended it as I was having really awful sweats, migraines and not sleeping well. This has stopped all of these. Hope that helps x

MaryF profile image
MaryFAdministrator in reply toglovebox

I also use this, I am not on Warfarin, but have used Serenity for years, and it does help. MaryF

AnnieAxVale profile image
AnnieAxVale

Thank you all.. some really useful replies.. much appreciated.. will seek out this cream :) Is it chemist on the street or online? :)

MaryF profile image
MaryFAdministrator in reply toAnnieAxVale

It is on line, but do check with your consultant first, and for Thyroid issues join Thyroid UK on this platform, these are the tests I regularly do: thyroiduk.org.uk/tuk/testin... I pay for them myself. MaryF

AnnieAxVale profile image
AnnieAxVale in reply toMaryF

Thanks.. I am a member of there also.. sadly I dont have that option to pay.. infact prob dont have the option to buy the cream at that price.. :(

MaryF profile image
MaryFAdministrator in reply toAnnieAxVale

A pot lasts a long time, I do understand things are pricey, I feel very annoyed that I pay for nearly everything! MaryF

AnnieAxVale profile image
AnnieAxVale

Re the Serenity Cream by Wellsprings . I read an article that these people use petro chemicals in their cream .. and Health Science are the ones who do not.. its got a little confusing to say the least..

donnabrain profile image
donnabrain

I am currently using black cahosh from holland and barrett

think its seven pounds

Has reduced (but not stopped) my flushes

Am sweating quite a lot , but, hey, we are actually getting a summer this year!

AnnieAxVale profile image
AnnieAxVale in reply todonnabrain

GP advised me to avoid that .. but ty )

panda60 profile image
panda60

I have been taking HRT for a while. Tried coming off it but completely lost my memory so my GP said go back on it and my APS consultant and gynae consultant said it is ok. I had an ablation and a mirena coil fitted for post-menopausal bleeding -coil releases progesterone and I use an oestrogen gel. (skin reaction to patches). I am on warfarin so well anticoagulated.

My personal choice of course, but I wouldn't change my decision.

Wittycjt profile image
Wittycjt

Maybe Paxil? Try searching it out. I am on warfarin and take this. See what you HCP thinks.. Let us know please

Not what you're looking for?

You may also like...

APS - Triple Positive High levels

Hi everyone! Im new here, posting... not so new reading as i have been reading everyones posts...

Re: APS diagnosis

Hi there, Just wondered is it standard procedure to be waiting 6 months for a diagnosis on APS. I...
tAigers profile image

Getting used to APS

Hi all, only just found this Forum, excellent stuff when you are feeling a little lost.... I...

APS and migraines

Can anyone here tell me how the migraines associated with APS and or testing positive for...
Brychni profile image

APS specialist referral & thyroid results

Good afternoon everyone I hope you are all having a lovely weekend, It’s been 5 weeks since my...
Hollyhughes profile image

Moderation team

See all
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator
lupus-support1 profile image
lupus-support1Administrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.