MSA and Hypotension: My husband has... - Multiple System A...

Multiple System Atrophy Trust

1,774 members1,425 posts

MSA and Hypotension

Ruffner profile image
9 Replies

My husband has been dx with MSA recently. His most disabling symptom is NOH. We are struggling with treating his low blood pressure and the resulting supine hypertension. He also has very low heart rates (sometimes 40-45 bpm) with SOB and "wooziness." He is worse in the morning. If he sits in his reclining chair he feels okay. How do you maintain some kind of physical exercise when doing so brings on symptomatic hypotension?

Written by
Ruffner profile image
Ruffner
To view profiles and participate in discussions please or .
9 Replies
J0nstandard profile image
J0nstandard

Hi - I care for my sister with MSA - so I know about the NOH blood pressure problem and agree that it’s a big reducer of quality of life. My sympathies.Can I ask if he is on any meds to try control this?

Ruffner profile image
Ruffner in reply toJ0nstandard

Thank you for replying. I would like to know more about your sister if you are comfortable sharing. He has been taking Midodrine for about a year with modest, unpredictable results. We have tried to increase the dose but doing so causes supine hypertension over 200/115. He is not supposed to lay down while on the medication but his coat hanger pain and nausea are improved if he lays down so I find him in bed several times during the day. He's frustrated, anxious, depressed and at times ready to give-up but I am not giving up.

J0nstandard profile image
J0nstandard in reply toRuffner

I’m happy to share about my sister’s condition yes. She has very erratic BP readings that result in dizziness and fatigue - sometimes high sometimes low. The drug (steroid) fludrocortisone is having some stabilising effect but that is hit and miss. As far as I understand it the autonomous part of the brain the controls or regulates blood pressure has been damaged/impaired as a result of the MSA. She says that nothing short of lying down will help the feeling of vertigo/dizziness these days. So the cortisone is helping to stabilise the BP - but there’s no relief from the woozy symptoms unfortunately.

This in turn makes her feel less hungry (a bit nauseous).

It may be worth asking your doctor to consider alternative blood pressure regulating meds to see if one is better than another for your husband.

My best wishes for you both - it’s a very tough ride this illness. All strength to you.

Make every day count!

Ruffner profile image
Ruffner in reply toJ0nstandard

I'm sorry about your sister - you must be a very special person to care for her. Your description of her symptoms sounds very much like my husband. He also has daily nausea (he describes it as gnawing). We will ask about the Fludrocortisone tomorrow at his appt. My husband also tells me that lying down gives him the most symptom relief but it comes with the price of very high blood pressure. Hoping the Fludro works! Thank you and my best to you and your sister.

binnyrox profile image
binnyrox

HelloI’m sorry to hear of your husbands situation. It used to be a problem for me but the following helped immensely

1. I am prescribed Florinef to be taken daily. This medication does not work immediately but helps maintain more stable readings overall

2. I test my BP often and when it starts to drop - I will take a Midodrine. The helpful effect typically lasts a few hours

3. I check my BP before engaging physical exercise. My bp falls 20-30points so I ensure it’s at least 130 otherwise the danger of a fall is there. (I’ve had stitches to the head ignoring this)

4. To bring BP up quickly, I drink 250ml very cold water with a liberal dose of salt. (I do not have any renal problems). That works very well for me.

5. To negate rising BP at night, I was asked to sleep on a trendelenburg bed. It works.

A simple alternative is to place a few bricks under the legs of the bed head side - so the mattress tilts like a plank towards the feet

Hope this helps

BR

Ruffner profile image
Ruffner in reply tobinnyrox

Thank you! We go to his neurologist tomorrow so I'll bring up the Florinef. My husband's typical blood pressure drop is 60-70 points immediately upon standing and well over 100 points if he continues to stand. Yesterday, we measured 65/44 after a very short walk (curiously, he does not pass out). We have a wedge under his mattress but I don't think we have it raised high enough so we'll look into that too. I've been a nagging wife about the water - I wish he could manage that part on his own. My best to you.

Janeyl profile image
Janeyl

This is quite an old article, but I found it helpful in trying to manage NOH, which was the worst of my husband’s symptoms. ncbi.nlm.nih.gov/pmc/articl...

Ruffner profile image
Ruffner

I've read a lot on the subject but the article you referenced is the most comprehensive. We are doing many of the strategies but I think more could be added. My husband doesn't seem to be able to manage this on his own so I need to be more involved. Thank you.

SaltyFlorist profile image
SaltyFlorist

I have been living with NOH for 9 years. I have turned my physical therapy exercises into a floor yoga routine so that I can remember each exercise. I started small. 1 set of 10 stomach exercises. I now do 30 minutes 4-5 times per week. I will also hold the stair railing with both hands 10 steps each leg. (Bottom stair only) My goal is to keep my core and legs strong to help keep me safe from falls. It also reduces my anxiety.I take midodrine and fludrocortisone. My doc said it’s pointless if I don’t keep up on the salt and water. I drink 48 oz of water and 2 salt tablets before I get out of bed in the AM. It still takes me 60-90 minutes before I can sit up without getting sick. (I also use compression wear.)

To help me stay hydrated I love mixing citrus Nuun tablets in with my peach tea, drinking Gatorade with additional salt added to it and eating a lot of soup. If I get too low on fluids I’m quite ruined for the day. I don’t recover and spend the rest of that day in bed. I average 2-3 liters of fluid per day. I hope this is helpful.

Not what you're looking for?

You may also like...

Low Blood Pressure and MSA

My husband has MSA and he really struggles with constantly feeling dizzy and lightheaded. His...
Redjune1 profile image

MSA affected by Covid

My husband who is 5 years into this dreadful condition is currently in hospital due to COVID...
Jud11 profile image

MSA progression

Hi All, I hope that you are managing to enjoy the sunshine as much as possible. I haven't been...
Hellebelle profile image

strokes and msa

my mum couldn’t wake my dad the other morning , so he was admitted to hospital -they seemed to...
chester2107 profile image

Possible MSA diagnosis?

My husband was diagnosed at 45 with Parkinson's, that was 4 years ago. Over the last 6 months his...
Jem2121 profile image

Moderation team

See all
MSATKirsten profile image
MSATKirstenAdministrator
JamesMSAT profile image
JamesMSATAdministrator
NicoleMSA profile image
NicoleMSAAdministrator

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.