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I Have Very Severe Poly Neuropathy What Can I Do? I Have To Use A Walker Nerve Damage Re EMG. Sudden Severe Pain Back Of Legs
A MyAmyloidosisTeam Member asked a question 💭

calf and hamstring muscles severe pain when standing or trying to walk

Foods To Avoid With Amyloidosis Read Article...
A MyAmyloidosisTeam Member

watch that your BP doesn't go too low if it does take hydrocortisone see Endocrinology amyloidosis specialist. Do your ankles swell feet etc do your retain fluid ? Do you take Lasix water pill. Whaya… read more

Organ Specific Primary Amyloidosis Can You Explain This Condition?
A MyAmyloidosisTeam Member asked a question 💭
A MyAmyloidosisTeam Member

I am suffering from primary Amyloidisis affected on kideny filtration so creatine increased to @8

Has Anyone Taken Tafamidis And Gotten Better?
A MyAmyloidosisTeam Member asked a question 💭
A MyAmyloidosisTeam Member

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Does Anyone Else Have Balance Issues?
A MyAmyloidosisTeam Member asked a question 💭

My husband who was diagnosed about a year ago, but who has had symptoms of CATTR for +12years has severe balance issues. Originally they were blamed on vestibular neuritis, but seem to worsen ever more frequently with "bouts" of imbalance and falls. Sometimes there is LOC, other times he is just soooo tired that he falls down. Drs seem to just shake their heads and seem to imply it is a separate issue
Has anyone else ever had inner ear nerve damage attributed to the amyloidosis?

A MyAmyloidosisTeam Member

I had a stroke in Cerebellum that I thought was cause of balance issues ( don’t know when), but I think it may be related. Had gotten worse lately. I have CM ATTR so it may have triggered the stroke.

Hi Dan From Calgary Asking After Taking 10 Mg Of Dex 2 Hours Before Treatment Increases Your Blood Pressure As Mine Seems To Go Up
A MyAmyloidosisTeam Member asked a question 💭
I Am Wondering If I Should Continue To Take Tafamidis As I Am In Stage Iiib Advanced Heart Failure?
A MyAmyloidosisTeam Member asked a question 💭

I have be taking Tafamidis since March 2022 with no positive changes. I was thinking that due to my advanced heart failure I may not see any benefit by continuing to take Tafamidis.

A MyAmyloidosisTeam Member

You should stay on meds. It helped my brother a lot. He got a heart transplant las November after thanksgiving and he is doing so good now. I hope I get a prescription soon.

My Eyes Have Gotten So Much Worse To The Extent That They Are Worse Than Any Other Of The Symptoms.
A MyAmyloidosisTeam Member asked a question 💭

Worse is the double and triple vision. I also get blurry eyes, and runny eyes. I frequently have to squint to see anything. Anyone had similar experiences? Any suggestions for help? Thanks, Bev H.

A MyAmyloidosisTeam Member

Thank you Cindy3!!!

ATTRwt : Has Anyone Verified Hearth Thickness After Using Tafamidis By Echocardiogram Versus The Thickness Before The Therapy?
A MyAmyloidosisTeam Member asked a question 💭

I think the only way to really understand how much Tafamidis works is by comparing the heath thickness before and after, at least 1 year of therapy. Has anyone got this information?

A MyAmyloidosisTeam Member

Sheldon, is the Acoramidis also manufactured by the same company as Tafamidis and Patisiran?

Has Anyone Here Been Referred To Palliative Care? My Hubby’s Pain Is Out Of Control, The Hematologist Referred Him Today.
A MyAmyloidosisTeam Member asked a question 💭
A MyAmyloidosisTeam Member

Palliative Care has been wonderful, they manage all his pain meds. The team is so caring, empathic and I couldn’t imagine managing this path without them.

Will The Site Be Putting Up Any New Material In The Resources Section? Some Of The Material Is From 2021… Maybe A Little Outdated 🤷🏻‍♀️
A MyAmyloidosisTeam Member asked a question 💭
A MyAmyloidosisTeam Member

Sean I’m sorry you’re not getting what you need from this site. I might have to agree to disagree on some of your points. I wish you the best on this journey we’re all on.