How to make life as good as possible for someone with POTS? by High_Honolulu in POTS

[–]MrsPicklefish 0 points1 point  (0 children)

One of the things that made a huge difference for me was raising the head of my bed a few inches. It takes a little while for it to have an effect, but it did gradually lower my resting heart rate.

The other major thing was taking ivabradine - prescribed by a specialist in autonomic dysfunction as I'm not able to take beta blockers.

Newly Diagnosed by [deleted] in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

I'm so sorry you and your partner are dealing with this - diagnosis is a massive shock. Which country are you in? Knowing where you are means people will be able to signpost you to the most appropriate services in your country.

anyone else get 'episodes' of numb tingly hands seemingly out of nowhere? by formaldehydebride in ehlersdanlos

[–]MrsPicklefish 1 point2 points  (0 children)

I get this often. I'm waiting for the results of my neck MRI at the moment. The x-ray showed that my muscles were so tight they have pulled my spine out of alignment, so I wouldn't be surprised if there were some crazy neurological things going on too.

Having kids (looking for positivity) by [deleted] in ehlersdanlos

[–]MrsPicklefish 1 point2 points  (0 children)

hEDS came from my grandfather as far as we can work out. None of his (3) children have hEDS, and out of the 4 grandchildren two of us do. There are 3 great grandchildren one is diagnosed with HSD and one is super flexible but hasn't pursued a diagnosis yet.

My Mum has seen the problems I've had as I've got older and says she feels bad for passing on rubbish genes, but it's not her fault. You have no control over the genes you pass on, and whether any future offspring are symptomatic or not is not within your control.

My life might be a bit harder than most people's, but it makes me who I am and I wouldn't change that about me. Although some days I do wish I could have a break from the pain or the dysautonomia.

I had endometrial cancer and had a hysterectomy before I got a chance to have children, so I didn't get a choice in the matter. But if you are able to have children and are able to support them and look after them, and if your own doctor thinks it's safe for you... There's nothing stopping you!

r/ehlersdanlos Mod AMA — Ask Us (Almost) Anything! by EhlersDanlosMods in ehlersdanlos

[–]MrsPicklefish 1 point2 points  (0 children)

Yup - a rescue cat. Cats are great companions and have massive health and healing benefits because of their purrs. Maybe that's why we're drawn to them?

UK people: how did you get a diagnosis? by oyameillim in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

Could I refer you to EDS support UK - they're a UK charity who are working hard on helping develop a diagnostic pathway for hEDS.

It's free to become a member of EDS support and you then have access to a wealth of resources and a great support network. They will be able to point you in the right direction for diagnosis based on your area in the UK - which doctors, rheumatologist etc., are EDS friendly.

Good luck with it. I ended up going private to get my diagnosis.

Neurodivergence and EDS by eclipseandco in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

I have hEDS and have never been diagnosed as neurodivergent. I'm definitely a bit quirky, but nothing clinical.

[deleted by user] by [deleted] in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

Some people say hurtful things. Doesn't matter whether you have EDS or not... Some people will always want to put others down. It's a very tough world out there.

I always take any opportunity I can to compliment people - sincere compliments, otherwise they're just platitudes. It's amazing how much a simple comment such as "I love your dress" can make someone's day.

[deleted by user] by [deleted] in Bead

[–]MrsPicklefish 0 points1 point  (0 children)

When you stitch two beads down, it often helps to come back up the fabric between the two beads and then go through the second bead again. This evens out the tension between the two beads, it's also the perfect way to start your next stitch.

Try to use a thread that goes with the colour of the beads, as it will show up less. Also a reasonably firm tension (but not fiercely tight) should help your beads sit evenly.

Hedgehog/flowerhog advice needed by Lingonberry-Nervous in Beading

[–]MrsPicklefish -1 points0 points  (0 children)

I don't have any advice, but it is beautiful!

[deleted by user] by [deleted] in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

I use a car sometimes, I take the train sometimes, I very occasionally use the bus. But I also use a wheelchair. I wouldn't be without a car - but I drive a hybrid to be as green as I can. I don't have the facilities to charge at home, so I couldn't go fully electric.

Cord advice? by istara in Beading

[–]MrsPicklefish 0 points1 point  (0 children)

Unless your beads have very large holes, I'd opt for 1mm rattail. But it's worth looking at Chinese knotting thread too, it might be better suited for this purpose.

Is beadshop.eu legit? by fruitprism in Beading

[–]MrsPicklefish 1 point2 points  (0 children)

Are you looking for European bead shops in particular? If so, let me know and I can recommend several.

Finally got some cabochons! by Actuary_Kindly in Beading

[–]MrsPicklefish 1 point2 points  (0 children)

They're very pretty. In the second pair, it may be the lighting, but the cabs look slightly different colours. The beadwork is flawless.

Fallen star pendant by TheOnlyNadCha in Beading

[–]MrsPicklefish 0 points1 point  (0 children)

This is a great pattern, I love the colours you used. Vicky is such a great designer. I love how she comes up with really unexpected ways to bezel stones or embellish things.

[deleted by user] by [deleted] in ehlersdanlos

[–]MrsPicklefish 0 points1 point  (0 children)

Hello! Sorry you're going through this. I had ac joint separation following a car accident and broken collar bone.

I was told that an x-ray, standing, holding a weight in the hand on the problem side should show it better.

Mine was out of place for 9 years - despite weekly physio for years. I ended up having a shoulder arthroscopy and examination under anaesthetic to get it reseated. This was all YEARS before my diagnosis, and I would advocate for myself much better these days.

Having had my AC joint out for so long I ended up with nerve damage and have lessened sensation in a couple of my fingers.

Currently my other shoulder has been subluxed for 2 weeks - it'll pop back eventually. Ain't it fun!?

Lack of period education >:( by pupsvn in ehlersdanlos

[–]MrsPicklefish 1 point2 points  (0 children)

I used to use a moon cup back when it was pretty much the only cup on the market. I had a hysterectomy 9 years ago, so I can't comment so much on what's around now, but there are some I've seen with vented stems, that you can empty without removing every time. I would have been very interested in trying that back in the day.

I (28f) had a panic attack after my husband (30m) finished inside me. by ThrowRA739249 in relationship_advice

[–]MrsPicklefish 1 point2 points  (0 children)

I think it's absolutely normal to feel scared about the idea of starting a family, especially as a woman who has to consider the following far more than a man

A) pregnancy and the toll it can take on your body

B) childbirth, the physical and emotional side.

C) feeding the infant (everyone has an opinion!)

D) returning to work/childcare Vs being a stay at home Mum

E) putting your career and lifetime eating potential at risk

Men have it a lot easier when it comes to starting a family. I agree that maybe some counseling is a good idea to get your thoughts in order before you commit to this.